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Subject Areas on Research
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A 29-year-old woman with sudden anemia and arterial oxygen desaturation.
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A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion.
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A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.
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A case of vanishing bile duct syndrome and IBD secondary to Hodgkin's lymphoma.
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A clinical syndrome in imported cows subjected to environmental stress in Sudan.
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A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).
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A fatal x-linked recessive reticuloendothelial syndrome with hyperglobulinemia. X-linked recessive reticuloendotheliosis.
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A history of the concept of atypical depression.
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A model of neural cross-talk and irritation in the pelvis: implications for the overlap of chronic pelvic pain disorders.
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A new syndrome: ascites, hyperbilirubinemia, and hypoalbuminemia after biochemical modulation of fluorouracil with N-phosphonacetyl-L-aspartate (PALA).
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A pathogenetic role for TNF alpha in the syndrome of cachexia, arthritis, and autoimmunity resulting from tristetraprolin (TTP) deficiency.
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A perspective on trials comparing enoxaparin and unfractionated heparin in the treatment of non-ST-elevation acute coronary syndromes.
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A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
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A radiologic syndrome after high dose chemotherapy and autologous bone marrow transplantation, with clinical and pathologic features of systemic candidiasis.
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A randomized, placebo-controlled trial of early eptifibatide for non-ST-segment elevation acute coronary syndromes.
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A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome.
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A role for sonic hedgehog signaling in the pathogenesis of human tracheoesophageal fistula.
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A spatio-temporal absorbing state model for disease and syndromic surveillance.
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A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.
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A tale of two countries: Insights from the differences in Canadian/American patterns of care for patients with acute coronary syndromes.
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A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
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A variant of the LRP4 gene affects the risk of chronic lymphocytic leukaemia transformation to Richter syndrome.
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A young patient with polyarthralgia and hearing loss: a case report of Muenke syndrome.
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A zebrafish model for the Shwachman-Diamond syndrome (SDS).
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ACC/AHA 2002 guideline update for exercise testing: summary article. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1997 Exercise Testing Guidelines).
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ACC/AHA/ASE 2003 guideline update for the clinical application of echocardiography: summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/ASE Committee to Update the 1997 Guidelines for the Clinical Application of Echocardiography).
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Abdominal migraine: prophylactic treatment and follow-up.
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Aberrant cortical development is driven by impaired cell cycle and translational control in a DDX3X syndrome model.
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Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.
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Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS?
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Acne agminata limited to the eyelids.
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Acute clopidogrel use and outcomes in patients with non-ST-segment elevation acute coronary syndromes undergoing coronary artery bypass surgery.
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Acute coronary syndromes and diabetes mellitus.
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Acute coronary syndromes in patients with diabetes mellitus: diagnosis, prognosis, and current management strategies.
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Acute encephalopathy and fatty hepatomegaly.
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Adherence to evidence-based therapies after discharge for acute coronary syndromes: an ongoing prospective, observational study.
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Adipose tissue in the filum terminale: a computed tomographic finding that may indicate tethering of the spinal cord.
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Advances in Imaging for the Management of Acute Aortic Syndromes: Focus on Transesophageal Echocardiography and Type-A Aortic Dissection for the Perioperative Echocardiographer.
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Agreement Between Child Self-report and Caregiver-Proxy Report for Symptoms and Functioning of Children Undergoing Cancer Treatment.
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Allergic response to medical products in patients with alpha-gal syndrome.
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Allograft loss in renal transplant recipients with cryptococcus neoformans associated immune reconstitution syndrome.
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Alpha1-adrenergic blockers and intraoperative floppy-iris syndrome.
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An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.
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An automated strategy for bedside aPTT determination and unfractionated heparin infusion adjustment in acute coronary syndromes: insights from PARAGON A.
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An unusual variant of familial preexcitation.
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Anaesthetic management of a parturient with the postural orthostatic tachycardia syndrome: a case report.
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Anesthetic management of a ventilator-dependent parturient with the King-Denborough syndrome.
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Anesthetic management of children with Moebius sequence.
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Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence.
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Antenatal sonographic features of Walker-Warburg syndrome. Value of endovaginal sonography.
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Anterior spinal artery syndrome?
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Anti-Jo-1 syndrome presenting as cryptogenic organizing pneumonia.
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Antibody responses to protein, polysaccharide, and phi X174 antigens in the hyperimmunoglobulinemia E (hyper-IgE) syndrome.
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Anticentromere antibody. Clinical Correlations and association with favorable prognosis in patients with scleroderma variants.
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Antidepressants in chronic pain syndromes.
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Antifibrinolytic therapy in the management of the Kasabach Merritt syndrome.
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Antiplatelet and antithrombin therapies in the acute coronary syndromes.
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Arthritis syndromes associated with human T cell lymphotropic virus type I infection.
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Arthrogryposis, renal tubular acidosis and cholestasis syndrome: spectrum of the clinical manifestations.
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Assessment of pediatric bowel and bladder dysfunction: a critical appraisal of the literature.
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Association between admission white blood cell count and one-year mortality in patients with acute coronary syndromes.
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Association of a cancer diagnosis with vulnerability and frailty in older Medicare beneficiaries.
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Association of intravenous morphine use and outcomes in acute coronary syndromes: results from the CRUSADE Quality Improvement Initiative.
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Association of neuropsychiatric symptoms and sub-syndromes with cognitive impairment in community-dwelling Asian elderly.
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Association of revascularisation with low mortality in non-ST elevation acute coronary syndrome, a report from GUSTO IV-ACS.
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Association of statin therapy with outcomes of acute coronary syndromes: the GRACE study.
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Attenuation of rebound ischemia after discontinuation of heparin therapy by glycoprotein IIb/IIIa inhibition with eptifibatide in patients with acute coronary syndromes: observations from the platelet IIb/IIIa in unstable angina: receptor suppression using integrilin therapy (PURSUIT) trial.
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Atypical imaging findings in a near-fatal case of posterior reversible encephalopathy syndrome in a child.
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Auricular acupuncture in the treatment of acute pain syndromes: A pilot study.
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Autosomal dominantly inherited generalized basaloid follicular hamartoma syndrome: report of a new disease in a North Carolina family.
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Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.
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Axenfeld-Rieger syndrome. A spectrum of developmental disorders.
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Bayesian adaptive trial design in acute heart failure syndromes: moving beyond the mega trial.
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Bilaminar interepithelial bodies within fingerprint dystrophy-like changes in bilateral iridocorneal endothelial syndrome.
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Biliary atresia-polysplenia syndrome: surgical and clinical relevance in liver transplantation.
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Binge eating disorder and night eating syndrome: psychological and behavioral characteristics.
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Bivalirudin during cardiopulmonary bypass in patients with previous or acute heparin-induced thrombocytopenia and heparin antibodies: results of the CHOOSE-ON trial.
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Blau syndrome and related genetic disorders causing childhood arthritis.
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Bleeding events with abciximab in acute coronary syndromes without early revascularization: An analysis of GUSTO IV-ACS.
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Bleeding in acute coronary syndromes.
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Blue Vision (Cyanopsia) Associated With TURP Syndrome: A Case Report.
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Brief clinical report and review: the Marden-Walker syndrome.
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Bronchoalveolar lavage as a tool to predict, diagnose and understand bronchiolitis obliterans syndrome.
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CD7+, CD4-, CD8- acute leukemia: a syndrome of malignant pluripotent lymphohematopoietic cells.
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Cancer cachexia syndrome in head and neck cancer patients: Part II. Pathophysiology.
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Cardiac rhabdomyosarcoma presenting as hypereosinophilic syndrome.
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Case Series of Thrombosis With Thrombocytopenia Syndrome After COVID-19 Vaccination-United States, December 2020 to August 2021.
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Cases from the Osler Medical Service at Johns Hopkins University. Zieve syndrome.
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Cerebrospinal fluid 5-hydroxyindoleacetic acid and homovanillic acid in the pediatric opsoclonus-myoclonus syndrome.
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Challenges in predicting the need for coronary artery bypass grafting at presentation in patients with non-ST-segment elevation acute coronary syndromes.
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Changes in patterns of coronary revascularization strategies for patients with acute coronary syndromes (from the CRUSADE Quality Improvement Initiative).
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Changing the model of care for patients with acute coronary syndromes.
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Characteristics, management, and outcomes of 5,557 patients age > or =90 years with acute coronary syndromes: results from the CRUSADE Initiative.
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Characterization of myocardial infarction as an end point in two large trials of acute coronary syndromes.
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Chest case of the day. Williams-Campbell syndrome.
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Childhood Cancer Symptom Cluster: Leukemia and Health-Related Quality of Life.
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Choanal atresia and associated anomalies.
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Chronic Lyme disease: the controversies and the science.
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Chronic ear surgery in patients with syndromes and multiple congenital malformations.
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Chronic multifocal retinal infiltrates in patients infected with human immunodeficiency virus.
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Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal.
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Cinaciguat, a soluble guanylate cyclase activator: results from the randomized, controlled, phase IIb COMPOSE programme in acute heart failure syndromes.
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Classification of epilepsy syndromes and role of genetic factors.
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Clinical Phenotyping for Pain Mechanisms in Urologic Chronic Pelvic Pain Syndromes: A MAPP Research Network Study.
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Clinical Relevance of Ischemia with Nonobstructive Coronary Arteries According to Coronary Microvascular Dysfunction.
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Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
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Clinical assessment of acute heart failure syndromes: emergency department through the early post-discharge period.
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Clinical characteristics, process of care, and outcomes of Hispanic patients presenting with non-ST-segment elevation acute coronary syndromes: results from Can Rapid risk stratification of Unstable angina patients Suppress ADverse outcomes with Early implementation of the ACC/AHA Guidelines (CRUSADE).
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Clinical development of pharmacologic agents for acute heart failure syndromes: a proposal for a mechanistic translational phase.
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Clinical outcomes in cytomegalovirus-positive Posner-Schlossman syndrome patients treated with topical ganciclovir therapy.
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Clinical significance of thrombocytopenia during a non-ST-elevation acute coronary syndrome. The platelet glycoprotein IIb/IIIa in unstable angina: receptor suppression using integrilin therapy (PURSUIT) trial experience.
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Clinical trials of pharmacological therapies in acute heart failure syndromes: lessons learned and directions forward.
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Clinical, electrocardiographic, and biochemical data for immediate risk stratification in acute coronary syndromes.
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Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 1: Pluridisciplinary perspective on their hemodynamics and morphomechanics.
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Clonal expansion of CD8+ BV8 T lymphocytes in bone marrow characterizes thymoma-associated B lymphopenia.
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Clopidogrel to treat patients with non-ST-segment elevation acute coronary syndromes after hospital discharge.
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Cnksr2 Loss in Mice Leads to Increased Neural Activity and Behavioral Phenotypes of Epilepsy-Aphasia Syndrome.
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Coexistent carpal tunnel syndrome and cervical radiculopathy (double crush syndrome).
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Cogan's syndrome.
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Cold provocation testing and hand-arm vibration syndrome--an audit of the results of the Department of Trade and Industry for the evaluation of miners (Br J Surg 2003; 90: 1076-1079).
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Cold provocation testing and hand-arm vibration syndrome--an audit of the results of the Department of Trade and Industry for the evaluation of miners (Br J Surg 2003; 90: 1076-1079).
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Commentary on: ferrokinetics in the syndrome of familial hypoferremic microcytic anemia with iron malabsorption.
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Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
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Comparison of amaurosis fugax and transient cerebral ischemia: a prospective clinical and arteriographic study.
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Comparison of benefits and complications of hirudin versus heparin for patients with acute coronary syndromes undergoing early percutaneous coronary intervention.
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Comparison of effectiveness of enoxaparin versus unfractionated heparin to reduce silent and clinically apparent acute myocardial infarction in patients presenting with non-ST-segment elevation acute coronary syndrome.
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Comparison of outcomes of patients with acute coronary syndromes with and without atrial fibrillation.
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Comparison of test-negative and syndrome-negative controls in SARS-CoV-2 vaccine effectiveness evaluations for preventing COVID-19 hospitalizations in the United States.
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Complete Response of a Young Woman With MYD88WT Bing-Neel Syndrome on Ibrutinib Monotherapy Following a Single Cycle of B Hyper-CVAD/IT MTX.
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Conceptualizing comorbid PTSD and depression among treatment-seeking, active duty military service members.
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Congenital ichthyosis with spastic paraplegia of adult onset.
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Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.
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Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome.
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Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
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Corneal endothelial cell abnormalities in an early stage of the iridocorneal endothelial syndrome.
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Coronary heart disease moderates the relationship of chronic stress with the metabolic syndrome.
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Correction of hypoprothrombinemia by immunosuppressive treatment of the lupus anticoagulant-hypoprothrombinemia syndrome.
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Correlation between the international consensus definition of the Cancer Anorexia-Cachexia Syndrome (CACS) and patient-centered outcomes in advanced non-small cell lung cancer.
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Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease.
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Cuboid Edema Syndrome Following Fixation of Proximal Fifth Metatarsal Fractures in Professional Athletes.
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Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhood.
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Cyclophosphamide therapy of severe systemic necrotizing vasculitis.
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Cylindroma (adenoid cystic carcinoma) causing unilateral cranial neuropathy.
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Cytokines and adhesion molecules in the pathogenesis of vasculitis.
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Cytomegalovirus pneumonitis is a risk for bronchiolitis obliterans syndrome in lung transplantation.
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DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.
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De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.
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De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
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De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
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Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia.
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Defects of ocular motility after stereotactic midbrain lesions in man.
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Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.
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Detrusor overactivity persisting at night and preceding nocturia in patients with overactive bladder syndrome: a nocturnal cystometrogram and polysomnogram study.
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Diagnosis and treatment of the systemic and cutaneous necrotizing vasculitis syndromes.
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Diagnostic and therapeutic approach to the patient with vasculitis.
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Diazoxide restores beta3-adrenergic receptor function in diet-induced obesity and diabetes.
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Dietl's crisis: a syndrome of episodic abdominal pain of urologic origin that may present to a gastroenterologist.
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Differential treatment benefit of platelet glycoprotein IIb/IIIa inhibition with percutaneous coronary intervention versus medical therapy for acute coronary syndromes: exploration of methods.
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Dimensions of Religiosity and PTSD Symptom Clusters in US Veterans and Active Duty Military.
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Direct thrombin inhibitors in acute coronary syndromes: effect in patients undergoing early percutaneous coronary intervention.
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Distal metaphyseal ulnar-shortening osteotomy: surgical technique.
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Distinct functions of Nijmegen breakage syndrome in ataxia telangiectasia mutated-dependent responses to DNA damage.
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Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25.
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Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.
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Donor hepatic function: a factor in postreperfusion syndrome.
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Drug rash with eosinophilia and systemic symptoms (DRESS syndrome).
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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.
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Dubowitz syndrome: a defect in the cholesterol biosynthetic pathway?
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Early corneal findings in Cogan's syndrome.
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Early invasive strategy for acute coronary syndromes without persistent ST-segment elevation: has the time come for 'drive-through' angiography?
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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease.
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Effect of hirudin vs heparin on haemostatic activity in patients with acute coronary syndromes; the GUSTO-IIb haemostasis substudy.
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Effects of repetitive transcranial magnetic stimulation (rTMS) on specific symptom clusters in depersonalization disorder (DPD).
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Effects of total-body digital photography on cancer worry in patients with atypical mole syndrome.
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Efficacy and safety of enoxaparin compared with unfractionated heparin in high-risk patients with non-ST-segment elevation acute coronary syndrome undergoing percutaneous coronary intervention in the Superior Yield of the New Strategy of Enoxaparin, Revascularization and Glycoprotein IIb/IIIa Inhibitors (SYNERGY) trial.
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Efficacy and safety of fondaparinux versus enoxaparin in patients with acute coronary syndromes undergoing percutaneous coronary intervention: results from the OASIS-5 trial.
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Electrophysiological basis and genetics of Brugada syndrome.
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Elevated body mass index and intermediate-term clinical outcomes after acute coronary syndromes.
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Elevated creatine kinase-MB with normal creatine kinase predicts worse outcomes in patients with acute coronary syndromes: results from 4 large clinical trials.
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Elevated soluble interleukin-2 receptor in childhood hemophagocytic histiocytic syndromes.
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End points for clinical trials in acute heart failure syndromes.
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Endothelial metaplasia in the iridocorneal endothelial syndrome.
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Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
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Epidemiology of cardiorenal syndrome.
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Epidemiology of cardiorenal syndrome.
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Epilepsy in KCNH1-related syndromes.
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Epithelial clara cell injury occurs in bronchiolitis obliterans syndrome after human lung transplantation.
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Escape from tolerance in the human X-linked autoimmunity-allergic disregulation syndrome and the Scurfy mouse.
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Estimated Global Proportions of Individuals With Persistent Fatigue, Cognitive, and Respiratory Symptom Clusters Following Symptomatic COVID-19 in 2020 and 2021.
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Estuary-associated syndrome in North Carolina: an occupational prevalence study.
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Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship.
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Evaluation of dyslipidemia in the emergency department: impact of cholesterol testing on subsequent therapy.
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Evaluation of preprocessing techniques for chief complaint classification.
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Evolution in cardiovascular care for elderly patients with non-ST-segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative.
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Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
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Extent of ST-segment depression and cardiac events in non-ST-segment elevation acute coronary syndromes.
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Facial pain from an elongated styloid process (Eagle's syndrome).
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Facilitatory effects of 4-aminopyridine on neuromuscular transmission in disease states.
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Familial occurrence of meralgia paraesthetica.
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Familial pancreatic cancer.
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Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters.
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Familial spinocerebellar degeneration with corneal dystrophy.
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Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs.
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Floppy eyelid syndrome as a subset of lax eyelid conditions: relationships and clinical relevance (an ASOPRS thesis).
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Foster Kennedy syndrome.
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Frailty and aging-associated syndromes in lung transplant candidates and recipients.
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Frequency of stent thrombosis after acute coronary syndromes (from the SYMPHONY and 2nd SYMPHONY trials).
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From guidelines to clinical practice: the impact of hospital and geographical characteristics on temporal trends in the management of acute coronary syndromes. The Global Registry of Acute Coronary Events (GRACE).
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Frozen shoulder syndrome: diagnostic and treatment strategies in the primary care setting.
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Fryns syndrome survivors and neurologic outcome.
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Further clinical and molecular delineation of the 15q24 microdeletion syndrome.
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Further data supporting that paclitaxel-associated acute pain syndrome is associated with development of peripheral neuropathy: North Central Cancer Treatment Group trial N08C1.
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GM-CSF inhibition reduces cytokine release syndrome and neuroinflammation but enhances CAR-T cell function in xenografts.
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Galectin 3 complements BNP in risk stratification in acute heart failure.
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Gender differences in associations between DSM-5 posttraumatic stress disorder symptom clusters and functional impairment in war veterans.
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Gender disparities in the diagnosis and treatment of non-ST-segment elevation acute coronary syndromes: large-scale observations from the CRUSADE (Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes With Early Implementation of the American College of Cardiology/American Heart Association Guidelines) National Quality Improvement Initiative.
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Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.
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Genetic generalized epilepsies.
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Genetic testing and tumor surveillance for children with cancer predisposition syndromes.
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Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy.
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Global mortality associated with 33 bacterial pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019.
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Glutamate receptor autoimmunity in Rasmussen's encephalitis.
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Glycoprotein IIb/IIIa inhibitors in acute coronary syndromes: pathophysiologic foundation and clinical findings.
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Growing Teratoma Syndrome of Testicular Origin.
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HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals.
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HLA and Cogan's syndrome.
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Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiency.
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Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.
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Healthcare for older adults in North America: challenges, successes and opportunities.
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Heart failure with preserved left ventricular systolic function among patients with non-ST-segment elevation acute coronary syndromes.
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Hemangioma, supraumbilical midline raphé, and coarctation of the aorta with a right aortic arch: single causal entity?
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Heparin dosing and outcome in acute coronary syndromes: the GUSTO-IIb experience. Global Use of Strategies to Open Occluded Coronary Arteries.
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Heparin-induced thrombocytopenia in the pediatric intensive care unit population.
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Hereditary progressive atrioventricular conduction defect. A new syndrome?
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Hereditary renal cell carcinoma in the Eker rat: a rodent familial cancer syndrome.
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Hereditary renal disease and preauricular pits: report of a kindred.
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Herpes simplex virus hepatitis after renal transplantation.
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High incidence of pacemaker syndrome in patients with sinus node dysfunction treated with ventricular-based pacing in the Mode Selection Trial (MOST).
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High prevalence of geriatric syndromes in older adults.
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High-dose intravenous methylprednisolone for Kasabach-Merritt syndrome.
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High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
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Histopathology of fungal rhinosinusitis.
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How I treat catastrophic thrombotic syndromes.
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Hubris syndrome: an acquired personality disorder? A study of US Presidents and UK Prime Ministers over the last 100 years.
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Hyaluronan contributes to bronchiolitis obliterans syndrome and stimulates lung allograft rejection through activation of innate immunity.
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Hyper IgM syndrome associated with defective CD40-mediated B cell activation.
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Hypercalcemia, hypercalciuria, and elevated calcitriol concentrations with autosomal dominant transmission due to CYP24A1 mutations: effects of ketoconazole therapy.
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Hyperinsulinism/Hyperammonemia Syndrome: a synopsis.
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Hyperlactataemia syndromes associated with HIV therapy.
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Identifying Symptom Clusters Among People Living With HIV on Antiretroviral Therapy in China: A Network Analysis.
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IgE Fc receptor positive T and B lymphocytes in patients with the hyper IgE syndrome.
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IgE Fc receptor positive T, B and NK cells in patients with the hyper-IgE syndrome.
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Iliopsoas bursitis: clinical features, radiographic findings, and disease associations.
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Image of the month.
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Immune reconstitution syndrome associated with opportunistic mycoses.
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Immunogold localisation of laminin in normal and exfoliative iris.
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Impact of bleeding severity on clinical outcomes among patients with acute coronary syndromes.
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Impact of encephalopathy on mortality in the sepsis syndrome. The Veterans Administration Systemic Sepsis Cooperative Study Group.
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Impact of lung transplant operation on bronchiolitis obliterans syndrome in patients with chronic obstructive pulmonary disease.
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Impact of major bleeding on 30-day mortality and clinical outcomes in patients with acute coronary syndromes: an analysis from the ACUITY Trial.
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Impact of on-site cardiac interventional facilities on management and outcome of patients with acute coronary syndromes.
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Improving acute coronary syndrome care: the ACC/AHA guidelines and critical pathways.
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Improving the care of patients with non-ST-elevation acute coronary syndromes in the emergency department: the CRUSADE initiative.
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Increased T follicular helper cells and germinal center B cells are required for cGVHD and bronchiolitis obliterans.
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Index of suspicion. Case 1: Infant who has respiratory distress. Case 2: Abnormal behavior, seizures, and altered sensorium in a 7-year-old boy. Case 3: Fever and dysphagia in a 4-year-old girl.
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Infantile glaucoma associated with the Diamond-Blackfan syndrome.
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Influence of Inflammatory and Oxidative Stress Pathways on Longitudinal Symptom Experiences in Children With Leukemia.
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Influence of clinical trial enrollment on the quality of care and outcomes for patients with non-ST-segment elevation acute coronary syndromes.
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Influence of coronary artery disease and coronary revascularization status on outcomes in patients with acute heart failure syndromes: a report from OPTIMIZE-HF (Organized Program to Initiate Lifesaving Treatment in Hospitalized Patients with Heart Failure).
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Inhaled steroids as prophylaxis for delayed pulmonary toxicity syndrome in breast cancer patients undergoing high-dose chemotherapy and autologous stem cell transplantation.
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Insulin resistance syndrome and cardiovascular disease: genetics and connections to skeletal muscle function.
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Insurance coverage and care of patients with non-ST-segment elevation acute coronary syndromes.
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Integrating GP IIb/IIIa inhibition into treatment strategies for acute ST-elevation myocardial infarction.
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Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15.
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Intraoperative floppy iris syndrome: report of a case and histopathologic analysis.
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Intratumoral consumption of indium-111 labeled platelets in a patient with hemangiomatosis and intravascular coagulation (Kasabach-Merritt syndrome).
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Iris vasculopathy in exfoliation syndrome. An immunocytochemical study.
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Is transplant operation important in determining posttransplant risk of bronchiolitis obliterans syndrome in lung transplant recipients?
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Jaffe-Campanacci syndrome. A case report and review of the literature.
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Jhum-jhum: neuropsychiatric symptoms in a Nepali village.
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Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.
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Juvenile primary fibromyalgia syndrome.
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Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?
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Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2.
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LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.
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LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein.
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Lambert-Eaton myasthenic syndrome: the lack of short-term in vitro effects of serum factors on neuromuscular transmission.
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Lamotrigine in absence and primary generalized epilepsies.
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Laryngeal and ocular granulation tissue formation in two Punjabi children: LOGIC syndrome.
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Latest developments in the assessment and management of chronic musculoskeletal pain syndromes in children.
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Lessons learned from clinical trials in acute heart failure: phase 3 drug trials.
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Lifetime comorbidity, lifetime history of psychosis and suicide attempts, and current symptoms of patients with deteriorated affective disorder.
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Lithium carbonate in pseudobulbar palsy.
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Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.
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Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.
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Long-term oral platelet glycoprotein IIb/IIIa receptor antagonism with sibrafiban after acute coronary syndromes: study design of the sibrafiban versus aspirin to yield maximum protection from ischemic heart events post-acute coronary syndromes (SYMPHONY) trial. Symphony Steering Committee.
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Long-term results after the glycoprotein IIb/IIIa inhibitor abciximab in unstable angina: one-year survival in the GUSTO IV-ACS (Global Use of Strategies To Open Occluded Coronary Arteries IV--Acute Coronary Syndrome) Trial.
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Longitudinal dimensionality of adolescent psychopathology: testing the differentiation hypothesis.
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Longitudinal study of neuropsychological functioning in patients on chronic hemodialysis: a preliminary report.
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Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
-
Low-molecular-weight heparins and glycoprotein IIb/IIIa inhibitors with percutaneous coronary intervention in acute coronary syndromes.
-
Lung transplantation for Williams-Campbell syndrome.
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Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model.
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Man-in-the-barrel syndrome after thoracoilium fusion.
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Management of patients with acute coronary syndromes in the United States by platelet glycoprotein IIb/IIIa inhibition. Insights from the platelet glycoprotein IIb/IIIa in unstable angina: receptor suppression using integrilin therapy (PURSUIT) trial.
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Management of severe lower abdominal or inguinal pain in high-performance athletes. PAIN (Performing Athletes with Abdominal or Inguinal Neuromuscular Pain Study Group).
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Management strategies for Mayer-Rokitansky-Kuster-Hauser related vaginal agenesis: a cost-effectiveness analysis.
-
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
-
Mean subaxial space available for the cord index as a novel method of measuring cervical spine geometry to predict the chronic stinger syndrome in American football players.
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Mesenteric Malperfusion Syndromes in Type A Aortic Dissection: Current Management Strategies.
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Mice lacking the p53-effector gene Gadd45a develop a lupus-like syndrome.
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Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome.
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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
-
Migraine.
-
Minimally invasive colopexy for pediatric Chilaiditi syndrome.
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Miscellaneous vasculitic syndromes including Behçet's disease and central nervous system vasculitis.
-
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.
-
Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
-
Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.
-
Modified varicella-like syndrome in children previously vaccinated with live attenuated measles, mumps, rubella and varicella vaccine.
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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
-
Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
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Molecular cross-talk among chromosome fragility syndromes.
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Mollaret meningitis. A report of three cases.
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Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA.
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Muir-Torre syndrome.
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Mullerian dysgenesis: a critical review of the literature.
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Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
-
Multidisciplinary assessment and diagnosis of conversion disorder in a patient with foreign accent syndrome.
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Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.
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Musculoskeletal syndromes associated with malignancy.
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Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.
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Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.
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Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
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Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.
-
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
-
Myasthenic syndrome caused by plectinopathy.
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Myoclonus and tremor response to thalamic deep brain stimulation parameters in a patient with inherited myoclonus-dystonia syndrome.
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Myopia predicts better outcome in persistent hyperplastic primary vitreous.
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Nager acrofacial dysostosis.
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National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines: clinical characteristics and utilization of biochemical markers in acute coronary syndromes.
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National Academy of Clinical Biochemistry and IFCC Committee for Standardization of Markers of Cardiac Damage Laboratory Medicine Practice Guidelines: analytical issues for biochemical markers of acute coronary syndromes.
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Natural history of paclitaxel-associated acute pain syndrome: prospective cohort study NCCTG N08C1.
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Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes.
-
Neural misdirection in congenital ocular fibrosis syndrome: implications and pathogenesis.
-
Neurocutaneous disease: Neurocutaneous dysesthesias.
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Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases.
-
Neuroligins provide molecular links between syndromic and nonsyndromic autism.
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Neuropathic Ocular Pain due to Dry Eye is Associated with Multiple Comorbid Chronic Pain Syndromes.
-
New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma.
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Non-communicable disease syndemics: poverty, depression, and diabetes among low-income populations.
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Nonoperative and operative management of snapping scapula.
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Normative data for vascular and neurological tests of the hand-arm vibration syndrome.
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Novel approach to the treatment of distal malperfusion secondary to ascending aortic dissection.
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Occult spontaneous esophageal perforation. Unusual clinical and radiographic presentation.
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On angiomas of retina, brain, and skin.
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Optimal use of nitrogen to suppress the high pressure nervous syndrome.
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Oral platelet glycoprotein IIb/IIIa inhibition.
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Outcomes of patients with acute coronary syndrome and previous coronary artery bypass grafting (from the Pravastatin or Atorvastatin Evaluation and Infection Therapy [PROVE IT-TIMI 22] and the Aggrastat to Zocor [A to Z] trials).
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Outcomes of patients with acute coronary syndromes and prior coronary artery bypass grafting: results from the platelet glycoprotein IIb/IIIa in unstable angina: receptor suppression using integrilin therapy (PURSUIT) trial.
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Ovarian dysmetabolic syndrome.
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Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndrome.
-
Overview of current noninodilator therapies for acute heart failure syndromes.
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PET Imaging of Dementia: Update 2022.
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PTEN loss in the continuum of common cancers, rare syndromes and mouse models.
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PURA Syndrome and Myotonia.
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Pain Syndromes and Management in Adult Hematopoietic Stem Cell Transplantation.
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Pain management strategies for thoracotomy and thoracic pain syndromes.
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Painful bone marrow edema syndrome of the foot and ankle.
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Pallister-Hall syndrome associated with an unbalanced chromosome translocation.
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Pan-aortic hybrid treatment of mega-aorta syndrome.
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Pancreatic insufficiency in Toriello-Carey syndrome: report of a second patient.
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Paraneoplastic limbic encephalopathy with testicular carcinoma. A reversible neurologic syndrome.
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Pathologic correlates of bronchiolitis obliterans syndrome in pulmonary retransplant recipients.
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Patterns of aspirin dosing in non-ST-elevation acute coronary syndromes in the CRUSADE Quality Improvement Initiative.
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Pediatric pain syndromes and management of pain in children and adolescents with rheumatic disease.
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Pediatric solid tumors and associated cancer predisposition syndromes: Workup, management, and surveillance. A summary from the APSA Cancer Committee.
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Pena-Shokeir type I syndrome: in utero sonographic appearance.
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Percutaneous coronary interventions in patients with heparin-induced thrombocytopenia.
-
Pharmacodynamics, pharmacokinetics, and safety of single-dose subcutaneous administration of selatogrel, a novel P2Y12 receptor antagonist, in patients with chronic coronary syndromes.
-
Pharmacokinetics and safety of TP10, soluble complement receptor 1, in infants undergoing cardiopulmonary bypass.
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Pharmacological treatment of elderly patients with acute coronary syndromes without persistent ST segment elevation.
-
Physical Activity, the Childhood Cancer Symptom Cluster-Leukemia, and Cognitive Function: A Longitudinal Mediation Analysis.
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Platelet activation in myocardial ischemic syndromes.
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Platypnea-Orthodeoxia Syndrome: To Shunt or Not to Shunt, That is the Question.
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Poland's syndrome associated with childhood non-Hodgkin's lymphoma.
-
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
-
Polysplenia with pulmonary arteriovenous malformations.
-
Population pharmacokinetics of micafungin in neonates and young infants.
-
Post-obstructive diuresis: a varied syndrome.
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Post-pericardiotomy syndrome after percutaneous balloon pericardiotomy.
-
Posterior axial corneal malformation and uveoretinal angiodysgenesis--a neurocristopathy?
-
Posterior fossa syndrome and long-term neuropsychological outcomes among children treated for medulloblastoma on a multi-institutional, prospective study.
-
Potassium clearance and reactive gliosis in the alumina gel lesion.
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Poverty, process of care, and outcome in acute coronary syndromes.
-
Pre-engraftment syndrome after myeloablative dual umbilical cord blood transplantation: risk factors and response to treatment.
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Predicting a late positive serum troponin in initially troponin-negative patients with non-ST-elevation acute coronary syndrome: clinical predictors and validated risk score results from the TIMI IIIB and GUSTO IIA studies.
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Prediction of risk of death and myocardial infarction in the six months after presentation with acute coronary syndrome: prospective multinational observational study (GRACE).
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Predictors of target organ damage in hypertensive blacks and whites.
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Prevalence, predictors, and outcomes of patients with non-ST-segment elevation myocardial infarction and insignificant coronary artery disease: results from the Can Rapid risk stratification of Unstable angina patients Suppress ADverse outcomes with Early implementation of the ACC/AHA Guidelines (CRUSADE) initiative.
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Prior aspirin use predicts worse outcomes in patients with non-ST-elevation acute coronary syndromes. PURSUIT Investigators. Platelet IIb/IIIa in Unstable angina: Receptor Suppression Using Integrilin Therapy.
-
Proceedings of the fifth international RASopathies symposium: When development and cancer intersect.
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Prognostic implications of abnormalities in renal function in patients with acute coronary syndromes.
-
Prognostic importance of new small Q waves following non-ST-elevation acute coronary syndromes.
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Prognostic value of ST segment depression in acute coronary syndromes: insights from PARAGON-A applied to GUSTO-IIb. PARAGON-A and GUSTO IIb Investigators. Platelet IIb/IIIa Antagonism for the Reduction of Acute Global Organization Network.
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Prognostic value of isolated troponin elevation across the spectrum of chest pain syndromes.
-
Prostaglandin F2alpha levels in human ovarian plasma in pregnancy and in a case of Halban's disease.
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
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Pseudo-Mirizzi syndrome in acute cholecystitis.
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Pulmonary hemorrhage syndrome as a manifestation of disseminated intravascular coagulation: analysis of ten cases.
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Pulmonary hypertension and sleep apnea.
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Pulmonary hypertension associated with portal hypertension in a child with Williams syndrome--a case report.
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Quantification of creatine and guanidinoacetate using GC-MS and LC-MS/MS for the detection of cerebral creatine deficiency syndromes.
-
Quantitative assessment of diffusion abnormalities in posterior reversible encephalopathy syndrome.
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Racial differences among high-risk patients presenting with non-ST-segment elevation acute coronary syndromes (results from the SYNERGY trial).
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Randomized COMparison of platelet inhibition with abciximab, tiRofiban and eptifibatide during percutaneous coronary intervention in acute coronary syndromes: the COMPARE trial. Comparison Of Measurements of Platelet aggregation with Aggrastat, Reopro, and Eptifibatide.
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Randomized evaluation of the efficacy of enoxaparin versus unfractionated heparin in high-risk patients with non-ST-segment elevation acute coronary syndromes receiving the glycoprotein IIb/IIIa inhibitor eptifibatide. Long-term results of the Integrilin and Enoxaparin Randomized Assessment of Acute Coronary Syndrome Treatment (INTERACT) trial.
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Rapid remodeling of the maxillary sinus in silent sinus syndrome.
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Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
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Rationale and clinical evidence for the use of GP IIb/IIIa inhibitors in acute coronary syndromes.
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Rationale and design of the GRACE (Global Registry of Acute Coronary Events) Project: a multinational registry of patients hospitalized with acute coronary syndromes.
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Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.
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Recurrent Hemispheric Stroke Syndromes in Symptomatic Atherosclerotic Internal Carotid Artery Occlusions: The Carotid Occlusion Surgery Study Randomized Trial.
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Red fingers syndrome in a patient with pseudolymphoma.
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Reflechi twòp--thinking too much: description of a cultural syndrome in Haiti's Central Plateau.
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Regional control after precision lymph node dissection for clinically evident melanoma metastasis.
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Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene.
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Relation between baseline risk and treatment decisions in non-ST elevation acute coronary syndromes: an examination of international practice patterns.
-
Relationship Between Central Obesity, General Obesity, Overactive Bladder Syndrome and Urinary Incontinence Among Male and Female Patients Seeking Care for Their Lower Urinary Tract Symptoms.
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Renal tubular insufficiency, cholestatic jaundice, and multiple congenital anomalies--a new multisystem syndrome.
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Resting-state functional connectivity predicts longitudinal pain symptom change in urologic chronic pelvic pain syndrome: a MAPP network study.
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Rheumatologic manifestations of cancer.
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Ring chromosome 17: phenotype variation by deletion size.
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Risk factors for ovarian cancers with and without microsatellite instability.
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Risk stratification in acute coronary syndromes: the need for continued vigilance in "low-risk" patients.
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ST-segment monitoring in patients with acute coronary syndromes.
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Sacral neuromodulation for the dysfunctional elimination syndrome: a single center experience with 20 children.
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Sacral neuromodulation in children with dysfunctional elimination syndrome: description of incisionless first stage and second stage without fluoroscopy.
-
Safety and efficacy of abciximab combined with dalteparin in treatment of acute coronary syndromes.
-
Scheimpflug imaging in late Capsular Bag Distention syndrome after phacoemulsification.
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Screening for Moral Injury: The Moral Injury Symptom Scale - Military Version Short Form.
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Seckel syndrome and moyamoya.
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Seeking the optimal aspirin dose in acute coronary syndromes.
-
Selective serotonin reuptake inhibitors for fibromyalgia syndrome.
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Self-discrepancies as predictors of vulnerability to distinct syndromes of chronic emotional distress.
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Self-healing juvenile cutaneous mucinosis.
-
Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease.
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Serotonin-lesion myoclonic syndromes. I. Neurochemical profile and S-1 receptor binding.
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Severe laryngomalacia and bronchomalacia in DiGeorge syndrome and CHARGE association.
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Six-month outcomes of percutaneous coronary balloon angioplasty in acute coronary syndromes: Results from the PURSUIT trial.
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Solution structure of the NaV1.2 C-terminal EF-hand domain.
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Somnolence syndrome after focal radiation therapy to the pineal region: case report and review of the literature.
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Spatiotemporal changes in along-tract profilometry of cerebellar peduncles in cerebellar mutism syndrome.
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Spontaneous intracranial hemorrhage and multiple intracranial aneurysms in a patient with Roberts/SC phocomelia syndrome.
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Spontaneous intracranial hypotension syndrome treated with fludrocortisone.
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Statin therapy--time to turn the focus from efficacy to implementation?
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Strategies of patient care in acute coronary syndromes: rationale for the Global Registry of Acute Coronary Events (GRACE) registry.
-
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
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Successful management of pain syndrome due to Angiostrongylus cantonensis by implantable spinal cord stimulator.
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Successful treatment of sudden hearing loss in Cogan's syndrome with corticosteroids.
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Surgical removal vs observation for subfoveal choroidal neovascularization, either associated with the ocular histoplasmosis syndrome or idiopathic: I. Ophthalmic findings from a randomized clinical trial: Submacular Surgery Trials (SST) Group H Trial: SST Report No. 9.
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Susac syndrome with transient inverted vision.
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Sustained ventricular arrhythmias among patients with acute coronary syndromes with no ST-segment elevation: incidence, predictors, and outcomes.
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Sweating in ectodermal dysplasia syndromes. A review.
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Symptom Clusters, Physical Activity, and Quality of Life: A Latent Class Analysis of Children During Maintenance Therapy for Leukemia.
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Symptom Management and Psychosocial Needs of Adults With Acute Myeloid Leukemia During Induction Treatment: A Pilot Study.
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Symptom Science: Advocating for Inclusion of Functional Genetic Polymorphisms.
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Symptom clusters in children.
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Symptoms of neurasthenia following earthquake trauma: re-examination of a discarded syndrome.
-
Systemic inflammatory response syndrome after human syngeneic intestinal transplantation: evidence for disruption of enterocyte barrier function.
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Takotsubo cardiomyopathy: an unusual syndrome mimicking an ST-elevation myocardial infarction.
-
Tapia's syndrome. The erratic evolution of an eponym.
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Temporal trends in the use of early cardiac catheterization in patients with non-ST-segment elevation acute coronary syndromes (results from CRUSADE).
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Tezosentan in patients with acute heart failure and acute coronary syndromes: design of the Randomized Intravenous Tezosentan study (RITZ-4).
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Tezosentan in patients with acute heart failure and acute coronary syndromes: results of the Randomized Intravenous TeZosentan Study (RITZ-4).
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The 'morning glory syndrome' - a mesodermal defect?
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The Editor's Roundtable: arterial thrombosis and acute coronary syndromes.
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The HLA antigens in Cogan's syndrome.
-
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family.
-
The J wave patterns and risk of sudden cardiac death in patients with coronary artery disease.
-
The London Fibromyalgia Epidemiology Study: direct health care costs of fibromyalgia syndrome in London, Canada.
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The London Fibromyalgia Epidemiology Study: the prevalence of fibromyalgia syndrome in London, Ontario.
-
The Longitudinal Parallel Process Analysis of Biomarkers of Oxidative Stress, Symptom Clusters, and Cognitive Function in Children With Leukemia.
-
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
-
The cardiofaciocutaneous syndrome.
-
The correlation between presenting ST-segment depression and the final size of acute myocardial infarcts in patients with acute coronary syndromes.
-
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
-
The early glycoprotein IIb/IIIa inhibition in non-ST-segment elevation acute coronary syndrome (EARLY ACS) trial: a randomized placebo-controlled trial evaluating the clinical benefits of early front-loaded eptifibatide in the treatment of patients with non-ST-segment elevation acute coronary syndrome--study design and rationale.
-
The editor's roundtable: management and treatment of non-ST-segment elevation in acute coronary syndromes.
-
The effect of alpha1-adrenergic receptor antagonist tamsulosin (Flomax) on iris dilator smooth muscle anatomy.
-
The evolving picture of microdeletion/microduplication syndromes in the age of microarray analysis: variable expressivity and genomic complexity.
-
The genetics of the J wave patterns.
-
The hepatopulmonary syndrome: radiologic findings in 10 patients.
-
The impact of emergency department structure and care processes in delivering care for non-ST-segment elevation acute coronary syndromes.
-
The implications of blood transfusions for patients with non-ST-segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative.
-
The intra-articular component of the subscapularis tendon: anatomic and histological correlation in reference to surgical release in patients with frozen-shoulder syndrome.
-
The obesity paradox in non-ST-segment elevation acute coronary syndromes: results from the Can Rapid risk stratification of Unstable angina patients Suppress ADverse outcomes with Early implementation of the American College of Cardiology/American Heart Association Guidelines Quality Improvement Initiative.
-
The ophthalmologic manifestations of the cardio-facio-cutaneous syndrome.
-
The peeling skin syndrome.
-
The preexcitation syndromes.
-
The primary megacystis syndrome.
-
The prognostic value of creatine kinase elevations extends across the whole spectrum of acute coronary syndromes.
-
The prognostic value of the admission and predischarge electrocardiogram in acute coronary syndromes: the GUSTO-IIb ECG Core Laboratory experience.
-
The prolonged burner syndrome.
-
The rationale for an acute heart failure syndromes clinical trials network.
-
The syndrome of 5-fluorouracil cardiotoxicity. An elusive cardiopathy.
-
The syndrome of frontal lobe epilepsy: characteristics and surgical management.
-
The syndrome of hyperostosis and hyperphosphatemia.
-
The trilateral retinoblastoma syndrome.
-
The uveal effusion syndrome and trans-scleral flow.
-
Three children with a syndrome of obesity and overgrowth, atypical psychosis, and seizures: a problem in neuropsychopharmacology.
-
Thrombocytopenia and absent radii (TAR) syndrome associated with horseshoe kidney.
-
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
-
Time-resolved MR angiography as a useful sequence for assessment of ovarian vein reflux.
-
Too much of a good thing? Tracing the history of the propofol infusion syndrome.
-
Townes-Brocks syndrome: twenty novel SALL1 mutations in sporadic and familial cases and refinement of the SALL1 hot spot region.
-
Transcholedochal cholecystolithotomy for a variant of Mirizzi's syndrome.
-
Transcription factor E2-2 is an essential and specific regulator of plasmacytoid dendritic cell development.
-
Treatment planning and biomechanics of distraction osteogenesis from an orthodontic perspective.
-
Troponin T and quantitative ST-segment depression offer complementary prognostic information in the risk stratification of acute coronary syndrome patients.
-
Troponin T levels and risk of 30-day outcomes in patients with the acute coronary syndrome: prospective verification in the GUSTO-IV trial.
-
Troponin and other cardiac markers: role in management of acute coronary syndromes.
-
Troponin-T and N-terminal pro-B-type natriuretic peptide predict mortality benefit from coronary revascularization in acute coronary syndromes: a GUSTO-IV substudy.
-
Two Cases of Late Shone Syndrome With Pulmonary Hypertension: Heart-Lung Transplant or Valve Surgery?
-
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.
-
Ultrasonographic measurement of induced myopia associated with capsular bag distention syndrome.
-
Ultrastructural study of Norrie's disease.
-
Ultrastructural study of the corneal epithelium in the recurrent erosion syndrome.
-
Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
-
Unilateral empyema as a complication of infectious mononucleosis: a pathogenic variant of Lemierre's syndrome.
-
Unusual complications of antipsychotic drugs.
-
Urologic chronic pelvic pain syndrome: insights from the MAPP Research Network.
-
Urologic syndrome associated with wire caging in AKR mice.
-
Use of hand carried ultrasound, B-type natriuretic peptide, and clinical assessment in identifying abnormal left ventricular filling pressures in patients referred for right heart catheterization.
-
Use of immunosuppressive agents in the treatment of severe ocular and vascular manifestations of Cogan's syndrome.
-
Use of multidetector computed tomography for the assessment of acute chest pain: a consensus statement of the North American Society of Cardiac Imaging and the European Society of Cardiac Radiology.
-
Use of multidetector computed tomography for the assessment of acute chest pain: a consensus statement of the North American Society of Cardiac Imaging and the European Society of Cardiac Radiology.
-
Use of proven therapies in non-ST-elevation acute coronary syndromes according to evidence-based risk stratification.
-
Usefulness of ST depression with T-wave inversion in leads V(4) to V(6) for predicting one-year mortality in non-ST-elevation acute coronary syndrome (from the Electrocardiographic Analysis of the Global Use of Strategies to Open Occluded Coronary Arteries IIB Trial).
-
Usefulness of biomarkers for predicting long-term mortality in patients with diabetes mellitus and non-ST-elevation acute coronary syndromes (a GUSTO IV substudy).
-
VATER and hydrocephalus: distinct syndrome?
-
VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD.
-
Validation of the English translation of the low anterior resection syndrome score.
-
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.
-
Vascular morphogenesis: tales of two syndromes.
-
Vitrectomy for vitreomacular traction syndrome with macular detachment.
-
Walker-Warburg syndrome.
-
Wellens syndrome: a life-saving diagnosis.
-
What is the frequency and functional and clinical significance of complex lesions in non-infarct-related arteries after fibrinolysis for acute ST-elevation myocardial infarction?
-
What's in a name? Eponyms in head and neck imaging.
-
When you hear hoof beats...do not forget the zebras.
-
Women's health issues with fibromyalgia syndrome.
-
[Livedoid vasculopathy with heterozygous factor V Leiden mutation and sticky platelet syndrome].
-
Keywords of People
-
Alexander, John Hunter Peel,
Professor of Medicine,
Medicine, Cardiology
-
Bennett, Vann,
George Barth Geller Distinguished Professor of Molecular Biology,
Duke Cancer Institute
-
Cohen-Wolkowiez, Michael,
Kiser-Arena Distinguished Professor,
Pediatrics, Infectious Diseases
-
Laskowitz, Daniel Todd,
Professor of Neurology,
Duke Science & Society
-
O'Connor, Christopher Michael,
Adjunct Professor in the Department of Medicine,
Medicine, Clinical Pharmacology
-
Pitt, Geoffrey Stuart,
Adjunct Professor in the Department of Medicine,
Medicine, Cardiology
-
Starmer, Charles Franklin,
Professor Emeritus of Computer Science,
Computer Science
-
Taylor, Gregory Alan,
Professor in Medicine,
Integrative Immunobiology
-
Turner, Dennis Alan,
Professor of Neurosurgery,
Biomedical Engineering
-
Yancy Jr., William Samuel,
Professor of Medicine,
Medicine, General Internal Medicine