Syndrome

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  Subject Areas on Research

  • A 29-year-old woman with sudden anemia and arterial oxygen desaturation. 
  • A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. 
  • A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. 
  • A case of vanishing bile duct syndrome and IBD secondary to Hodgkin's lymphoma. 
  • A clinical syndrome in imported cows subjected to environmental stress in Sudan. 
  • A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). 
  • A fatal x-linked recessive reticuloendothelial syndrome with hyperglobulinemia. X-linked recessive reticuloendotheliosis. 
  • A history of the concept of atypical depression. 
  • A model of neural cross-talk and irritation in the pelvis: implications for the overlap of chronic pelvic pain disorders. 
  • A new syndrome: ascites, hyperbilirubinemia, and hypoalbuminemia after biochemical modulation of fluorouracil with N-phosphonacetyl-L-aspartate (PALA). 
  • A pathogenetic role for TNF alpha in the syndrome of cachexia, arthritis, and autoimmunity resulting from tristetraprolin (TTP) deficiency. 
  • A perspective on trials comparing enoxaparin and unfractionated heparin in the treatment of non-ST-elevation acute coronary syndromes. 
  • A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. 
  • A radiologic syndrome after high dose chemotherapy and autologous bone marrow transplantation, with clinical and pathologic features of systemic candidiasis. 
  • A randomized, placebo-controlled trial of early eptifibatide for non-ST-segment elevation acute coronary syndromes. 
  • A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome. 
  • A role for sonic hedgehog signaling in the pathogenesis of human tracheoesophageal fistula. 
  • A spatio-temporal absorbing state model for disease and syndromic surveillance. 
  • A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations. 
  • A tale of two countries: Insights from the differences in Canadian/American patterns of care for patients with acute coronary syndromes. 
  • A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27. 
  • A variant of the LRP4 gene affects the risk of chronic lymphocytic leukaemia transformation to Richter syndrome. 
  • A young patient with polyarthralgia and hearing loss: a case report of Muenke syndrome. 
  • A zebrafish model for the Shwachman-Diamond syndrome (SDS). 
  • 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). 
  • 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). 
  • Abdominal migraine: prophylactic treatment and follow-up. 
  • Aberrant cortical development is driven by impaired cell cycle and translational control in a DDX3X syndrome model. 
  • Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. 
  • Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS? 
  • Acne agminata limited to the eyelids. 
  • Acute clopidogrel use and outcomes in patients with non-ST-segment elevation acute coronary syndromes undergoing coronary artery bypass surgery. 
  • Acute coronary syndromes and diabetes mellitus. 
  • Acute coronary syndromes in patients with diabetes mellitus: diagnosis, prognosis, and current management strategies. 
  • Acute encephalopathy and fatty hepatomegaly. 
  • Adherence to evidence-based therapies after discharge for acute coronary syndromes: an ongoing prospective, observational study. 
  • Adipose tissue in the filum terminale: a computed tomographic finding that may indicate tethering of the spinal cord. 
  • Advances in Imaging for the Management of Acute Aortic Syndromes: Focus on Transesophageal Echocardiography and Type-A Aortic Dissection for the Perioperative Echocardiographer. 
  • Agreement Between Child Self-report and Caregiver-Proxy Report for Symptoms and Functioning of Children Undergoing Cancer Treatment. 
  • Allergic response to medical products in patients with alpha-gal syndrome. 
  • Allograft loss in renal transplant recipients with cryptococcus neoformans associated immune reconstitution syndrome. 
  • Alpha1-adrenergic blockers and intraoperative floppy-iris syndrome. 
  • An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS. 
  • An automated strategy for bedside aPTT determination and unfractionated heparin infusion adjustment in acute coronary syndromes: insights from PARAGON A. 
  • An unusual variant of familial preexcitation. 
  • Anaesthetic management of a parturient with the postural orthostatic tachycardia syndrome: a case report. 
  • Anesthetic management of a ventilator-dependent parturient with the King-Denborough syndrome. 
  • Anesthetic management of children with Moebius sequence. 
  • Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence. 
  • Antenatal sonographic features of Walker-Warburg syndrome. Value of endovaginal sonography. 
  • Anterior spinal artery syndrome? 
  • Anti-Jo-1 syndrome presenting as cryptogenic organizing pneumonia. 
  • Antibody responses to protein, polysaccharide, and phi X174 antigens in the hyperimmunoglobulinemia E (hyper-IgE) syndrome. 
  • Anticentromere antibody. Clinical Correlations and association with favorable prognosis in patients with scleroderma variants. 
  • Antidepressants in chronic pain syndromes. 
  • Antifibrinolytic therapy in the management of the Kasabach Merritt syndrome. 
  • Antiplatelet and antithrombin therapies in the acute coronary syndromes. 
  • Arthritis syndromes associated with human T cell lymphotropic virus type I infection. 
  • Arthrogryposis, renal tubular acidosis and cholestasis syndrome: spectrum of the clinical manifestations. 
  • Assessment of pediatric bowel and bladder dysfunction: a critical appraisal of the literature. 
  • Association between admission white blood cell count and one-year mortality in patients with acute coronary syndromes. 
  • Association of a cancer diagnosis with vulnerability and frailty in older Medicare beneficiaries. 
  • Association of intravenous morphine use and outcomes in acute coronary syndromes: results from the CRUSADE Quality Improvement Initiative. 
  • Association of neuropsychiatric symptoms and sub-syndromes with cognitive impairment in community-dwelling Asian elderly. 
  • Association of revascularisation with low mortality in non-ST elevation acute coronary syndrome, a report from GUSTO IV-ACS. 
  • Association of statin therapy with outcomes of acute coronary syndromes: the GRACE study. 
  • 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. 
  • Atypical imaging findings in a near-fatal case of posterior reversible encephalopathy syndrome in a child. 
  • Auricular acupuncture in the treatment of acute pain syndromes: A pilot study. 
  • Autosomal dominantly inherited generalized basaloid follicular hamartoma syndrome: report of a new disease in a North Carolina family. 
  • Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3. 
  • Axenfeld-Rieger syndrome. A spectrum of developmental disorders. 
  • Bayesian adaptive trial design in acute heart failure syndromes: moving beyond the mega trial. 
  • Bilaminar interepithelial bodies within fingerprint dystrophy-like changes in bilateral iridocorneal endothelial syndrome. 
  • Biliary atresia-polysplenia syndrome: surgical and clinical relevance in liver transplantation. 
  • Binge eating disorder and night eating syndrome: psychological and behavioral characteristics. 
  • Bivalirudin during cardiopulmonary bypass in patients with previous or acute heparin-induced thrombocytopenia and heparin antibodies: results of the CHOOSE-ON trial. 
  • Blau syndrome and related genetic disorders causing childhood arthritis. 
  • Bleeding events with abciximab in acute coronary syndromes without early revascularization: An analysis of GUSTO IV-ACS. 
  • Bleeding in acute coronary syndromes. 
  • Blue Vision (Cyanopsia) Associated With TURP Syndrome: A Case Report. 
  • Brief clinical report and review: the Marden-Walker syndrome. 
  • Bronchoalveolar lavage as a tool to predict, diagnose and understand bronchiolitis obliterans syndrome. 
  • CD7+, CD4-, CD8- acute leukemia: a syndrome of malignant pluripotent lymphohematopoietic cells. 
  • Cancer cachexia syndrome in head and neck cancer patients: Part II. Pathophysiology. 
  • Cardiac rhabdomyosarcoma presenting as hypereosinophilic syndrome. 
  • Case Series of Thrombosis With Thrombocytopenia Syndrome After COVID-19 Vaccination-United States, December 2020 to August 2021. 
  • Cases from the Osler Medical Service at Johns Hopkins University. Zieve syndrome. 
  • Cerebrospinal fluid 5-hydroxyindoleacetic acid and homovanillic acid in the pediatric opsoclonus-myoclonus syndrome. 
  • Challenges in predicting the need for coronary artery bypass grafting at presentation in patients with non-ST-segment elevation acute coronary syndromes. 
  • Changes in patterns of coronary revascularization strategies for patients with acute coronary syndromes (from the CRUSADE Quality Improvement Initiative). 
  • Changing the model of care for patients with acute coronary syndromes. 
  • Characteristics, management, and outcomes of 5,557 patients age > or =90 years with acute coronary syndromes: results from the CRUSADE Initiative. 
  • Characterization of myocardial infarction as an end point in two large trials of acute coronary syndromes. 
  • Chest case of the day. Williams-Campbell syndrome. 
  • Childhood Cancer Symptom Cluster: Leukemia and Health-Related Quality of Life. 
  • Choanal atresia and associated anomalies. 
  • Chronic Lyme disease: the controversies and the science. 
  • Chronic ear surgery in patients with syndromes and multiple congenital malformations. 
  • Chronic multifocal retinal infiltrates in patients infected with human immunodeficiency virus. 
  • Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal. 
  • Cinaciguat, a soluble guanylate cyclase activator: results from the randomized, controlled, phase IIb COMPOSE programme in acute heart failure syndromes. 
  • Classification of epilepsy syndromes and role of genetic factors. 
  • Clinical Phenotyping for Pain Mechanisms in Urologic Chronic Pelvic Pain Syndromes: A MAPP Research Network Study. 
  • Clinical Relevance of Ischemia with Nonobstructive Coronary Arteries According to Coronary Microvascular Dysfunction. 
  • Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome. 
  • Clinical assessment of acute heart failure syndromes: emergency department through the early post-discharge period. 
  • 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). 
  • Clinical development of pharmacologic agents for acute heart failure syndromes: a proposal for a mechanistic translational phase. 
  • Clinical outcomes in cytomegalovirus-positive Posner-Schlossman syndrome patients treated with topical ganciclovir therapy. 
  • 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. 
  • Clinical trials of pharmacological therapies in acute heart failure syndromes: lessons learned and directions forward. 
  • Clinical, electrocardiographic, and biochemical data for immediate risk stratification in acute coronary syndromes. 
  • Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 1: Pluridisciplinary perspective on their hemodynamics and morphomechanics. 
  • Clonal expansion of CD8+ BV8 T lymphocytes in bone marrow characterizes thymoma-associated B lymphopenia. 
  • Clopidogrel to treat patients with non-ST-segment elevation acute coronary syndromes after hospital discharge. 
  • Cnksr2 Loss in Mice Leads to Increased Neural Activity and Behavioral Phenotypes of Epilepsy-Aphasia Syndrome. 
  • Coexistent carpal tunnel syndrome and cervical radiculopathy (double crush syndrome). 
  • Cogan's syndrome. 
  • 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). 
  • 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). 
  • Commentary on: ferrokinetics in the syndrome of familial hypoferremic microcytic anemia with iron malabsorption. 
  • Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. 
  • Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. 
  • Comparison of amaurosis fugax and transient cerebral ischemia: a prospective clinical and arteriographic study. 
  • Comparison of benefits and complications of hirudin versus heparin for patients with acute coronary syndromes undergoing early percutaneous coronary intervention. 
  • 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. 
  • Comparison of outcomes of patients with acute coronary syndromes with and without atrial fibrillation. 
  • Comparison of test-negative and syndrome-negative controls in SARS-CoV-2 vaccine effectiveness evaluations for preventing COVID-19 hospitalizations in the United States. 
  • Complete Response of a Young Woman With MYD88WT Bing-Neel Syndrome on Ibrutinib Monotherapy Following a Single Cycle of B Hyper-CVAD/IT MTX. 
  • Conceptualizing comorbid PTSD and depression among treatment-seeking, active duty military service members. 
  • Congenital ichthyosis with spastic paraplegia of adult onset. 
  • Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature. 
  • Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome. 
  • Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18? 
  • Corneal endothelial cell abnormalities in an early stage of the iridocorneal endothelial syndrome. 
  • Coronary heart disease moderates the relationship of chronic stress with the metabolic syndrome. 
  • Correction of hypoprothrombinemia by immunosuppressive treatment of the lupus anticoagulant-hypoprothrombinemia syndrome. 
  • Correlation between the international consensus definition of the Cancer Anorexia-Cachexia Syndrome (CACS) and patient-centered outcomes in advanced non-small cell lung cancer. 
  • Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease. 
  • Cuboid Edema Syndrome Following Fixation of Proximal Fifth Metatarsal Fractures in Professional Athletes. 
  • Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhood. 
  • Cyclophosphamide therapy of severe systemic necrotizing vasculitis. 
  • Cylindroma (adenoid cystic carcinoma) causing unilateral cranial neuropathy. 
  • Cytokines and adhesion molecules in the pathogenesis of vasculitis. 
  • Cytomegalovirus pneumonitis is a risk for bronchiolitis obliterans syndrome in lung transplantation. 
  • DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes. 
  • De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome. 
  • De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas. 
  • De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. 
  • De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. 
  • Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia. 
  • Defects of ocular motility after stereotactic midbrain lesions in man. 
  • Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. 
  • Detrusor overactivity persisting at night and preceding nocturia in patients with overactive bladder syndrome: a nocturnal cystometrogram and polysomnogram study. 
  • Diagnosis and treatment of the systemic and cutaneous necrotizing vasculitis syndromes. 
  • Diagnostic and therapeutic approach to the patient with vasculitis. 
  • Diazoxide restores beta3-adrenergic receptor function in diet-induced obesity and diabetes. 
  • Dietl's crisis: a syndrome of episodic abdominal pain of urologic origin that may present to a gastroenterologist. 
  • Differential treatment benefit of platelet glycoprotein IIb/IIIa inhibition with percutaneous coronary intervention versus medical therapy for acute coronary syndromes: exploration of methods. 
  • Dimensions of Religiosity and PTSD Symptom Clusters in US Veterans and Active Duty Military. 
  • Direct thrombin inhibitors in acute coronary syndromes: effect in patients undergoing early percutaneous coronary intervention. 
  • Distal metaphyseal ulnar-shortening osteotomy: surgical technique. 
  • Distinct functions of Nijmegen breakage syndrome in ataxia telangiectasia mutated-dependent responses to DNA damage. 
  • Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25. 
  • Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome. 
  • Donor hepatic function: a factor in postreperfusion syndrome. 
  • Drug rash with eosinophilia and systemic symptoms (DRESS syndrome). 
  • Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia. 
  • Dubowitz syndrome: a defect in the cholesterol biosynthetic pathway? 
  • Early corneal findings in Cogan's syndrome. 
  • Early invasive strategy for acute coronary syndromes without persistent ST-segment elevation: has the time come for 'drive-through' angiography? 
  • Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. 
  • Effect of hirudin vs heparin on haemostatic activity in patients with acute coronary syndromes; the GUSTO-IIb haemostasis substudy. 
  • Effects of repetitive transcranial magnetic stimulation (rTMS) on specific symptom clusters in depersonalization disorder (DPD). 
  • Effects of total-body digital photography on cancer worry in patients with atypical mole syndrome. 
  • 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. 
  • Efficacy and safety of fondaparinux versus enoxaparin in patients with acute coronary syndromes undergoing percutaneous coronary intervention: results from the OASIS-5 trial. 
  • Electrophysiological basis and genetics of Brugada syndrome. 
  • Elevated body mass index and intermediate-term clinical outcomes after acute coronary syndromes. 
  • Elevated creatine kinase-MB with normal creatine kinase predicts worse outcomes in patients with acute coronary syndromes: results from 4 large clinical trials. 
  • Elevated soluble interleukin-2 receptor in childhood hemophagocytic histiocytic syndromes. 
  • End points for clinical trials in acute heart failure syndromes. 
  • Endothelial metaplasia in the iridocorneal endothelial syndrome. 
  • Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome. 
  • Epidemiology of cardiorenal syndrome. 
  • Epidemiology of cardiorenal syndrome. 
  • Epilepsy in KCNH1-related syndromes. 
  • Epithelial clara cell injury occurs in bronchiolitis obliterans syndrome after human lung transplantation. 
  • Escape from tolerance in the human X-linked autoimmunity-allergic disregulation syndrome and the Scurfy mouse. 
  • Estimated Global Proportions of Individuals With Persistent Fatigue, Cognitive, and Respiratory Symptom Clusters Following Symptomatic COVID-19 in 2020 and 2021. 
  • Estuary-associated syndrome in North Carolina: an occupational prevalence study. 
  • Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship. 
  • Evaluation of dyslipidemia in the emergency department: impact of cholesterol testing on subsequent therapy. 
  • Evaluation of preprocessing techniques for chief complaint classification. 
  • Evolution in cardiovascular care for elderly patients with non-ST-segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative. 
  • Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. 
  • Extent of ST-segment depression and cardiac events in non-ST-segment elevation acute coronary syndromes. 
  • Facial pain from an elongated styloid process (Eagle's syndrome). 
  • Facilitatory effects of 4-aminopyridine on neuromuscular transmission in disease states. 
  • Familial occurrence of meralgia paraesthetica. 
  • Familial pancreatic cancer. 
  • Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters. 
  • Familial spinocerebellar degeneration with corneal dystrophy. 
  • Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs. 
  • Floppy eyelid syndrome as a subset of lax eyelid conditions: relationships and clinical relevance (an ASOPRS thesis). 
  • Foster Kennedy syndrome. 
  • Frailty and aging-associated syndromes in lung transplant candidates and recipients. 
  • Frequency of stent thrombosis after acute coronary syndromes (from the SYMPHONY and 2nd SYMPHONY trials). 
  • 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). 
  • Frozen shoulder syndrome: diagnostic and treatment strategies in the primary care setting. 
  • Fryns syndrome survivors and neurologic outcome. 
  • Further clinical and molecular delineation of the 15q24 microdeletion syndrome. 
  • Further data supporting that paclitaxel-associated acute pain syndrome is associated with development of peripheral neuropathy: North Central Cancer Treatment Group trial N08C1. 
  • GM-CSF inhibition reduces cytokine release syndrome and neuroinflammation but enhances CAR-T cell function in xenografts. 
  • Galectin 3 complements BNP in risk stratification in acute heart failure. 
  • Gender differences in associations between DSM-5 posttraumatic stress disorder symptom clusters and functional impairment in war veterans. 
  • 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. 
  • Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression. 
  • Genetic generalized epilepsies. 
  • Genetic testing and tumor surveillance for children with cancer predisposition syndromes. 
  • Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy. 
  • Global mortality associated with 33 bacterial pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019. 
  • Glutamate receptor autoimmunity in Rasmussen's encephalitis. 
  • Glycoprotein IIb/IIIa inhibitors in acute coronary syndromes: pathophysiologic foundation and clinical findings. 
  • Growing Teratoma Syndrome of Testicular Origin. 
  • 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. 
  • HLA and Cogan's syndrome. 
  • Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiency. 
  • Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder. 
  • Healthcare for older adults in North America: challenges, successes and opportunities. 
  • Heart failure with preserved left ventricular systolic function among patients with non-ST-segment elevation acute coronary syndromes. 
  • Hemangioma, supraumbilical midline raphé, and coarctation of the aorta with a right aortic arch: single causal entity? 
  • Heparin dosing and outcome in acute coronary syndromes: the GUSTO-IIb experience. Global Use of Strategies to Open Occluded Coronary Arteries. 
  • Heparin-induced thrombocytopenia in the pediatric intensive care unit population. 
  • Hereditary progressive atrioventricular conduction defect. A new syndrome? 
  • Hereditary renal cell carcinoma in the Eker rat: a rodent familial cancer syndrome. 
  • Hereditary renal disease and preauricular pits: report of a kindred. 
  • Herpes simplex virus hepatitis after renal transplantation. 
  • High incidence of pacemaker syndrome in patients with sinus node dysfunction treated with ventricular-based pacing in the Mode Selection Trial (MOST). 
  • High prevalence of geriatric syndromes in older adults. 
  • High-dose intravenous methylprednisolone for Kasabach-Merritt syndrome. 
  • 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. 
  • Histopathology of fungal rhinosinusitis. 
  • How I treat catastrophic thrombotic syndromes. 
  • Hubris syndrome: an acquired personality disorder? A study of US Presidents and UK Prime Ministers over the last 100 years. 
  • Hyaluronan contributes to bronchiolitis obliterans syndrome and stimulates lung allograft rejection through activation of innate immunity. 
  • Hyper IgM syndrome associated with defective CD40-mediated B cell activation. 
  • Hypercalcemia, hypercalciuria, and elevated calcitriol concentrations with autosomal dominant transmission due to CYP24A1 mutations: effects of ketoconazole therapy. 
  • Hyperinsulinism/Hyperammonemia Syndrome: a synopsis. 
  • Hyperlactataemia syndromes associated with HIV therapy. 
  • Identifying Symptom Clusters Among People Living With HIV on Antiretroviral Therapy in China: A Network Analysis. 
  • IgE Fc receptor positive T and B lymphocytes in patients with the hyper IgE syndrome. 
  • IgE Fc receptor positive T, B and NK cells in patients with the hyper-IgE syndrome. 
  • Iliopsoas bursitis: clinical features, radiographic findings, and disease associations. 
  • Image of the month. 
  • Immune reconstitution syndrome associated with opportunistic mycoses. 
  • Immunogold localisation of laminin in normal and exfoliative iris. 
  • Impact of bleeding severity on clinical outcomes among patients with acute coronary syndromes. 
  • Impact of encephalopathy on mortality in the sepsis syndrome. The Veterans Administration Systemic Sepsis Cooperative Study Group. 
  • Impact of lung transplant operation on bronchiolitis obliterans syndrome in patients with chronic obstructive pulmonary disease. 
  • Impact of major bleeding on 30-day mortality and clinical outcomes in patients with acute coronary syndromes: an analysis from the ACUITY Trial. 
  • Impact of on-site cardiac interventional facilities on management and outcome of patients with acute coronary syndromes. 
  • Improving acute coronary syndrome care: the ACC/AHA guidelines and critical pathways. 
  • Improving the care of patients with non-ST-elevation acute coronary syndromes in the emergency department: the CRUSADE initiative. 
  • Increased T follicular helper cells and germinal center B cells are required for cGVHD and bronchiolitis obliterans. 
  • 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. 
  • Infantile glaucoma associated with the Diamond-Blackfan syndrome. 
  • Influence of Inflammatory and Oxidative Stress Pathways on Longitudinal Symptom Experiences in Children With Leukemia. 
  • Influence of clinical trial enrollment on the quality of care and outcomes for patients with non-ST-segment elevation acute coronary syndromes. 
  • 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). 
  • Inhaled steroids as prophylaxis for delayed pulmonary toxicity syndrome in breast cancer patients undergoing high-dose chemotherapy and autologous stem cell transplantation. 
  • Insulin resistance syndrome and cardiovascular disease: genetics and connections to skeletal muscle function. 
  • Insurance coverage and care of patients with non-ST-segment elevation acute coronary syndromes. 
  • Integrating GP IIb/IIIa inhibition into treatment strategies for acute ST-elevation myocardial infarction. 
  • Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15. 
  • Intraoperative floppy iris syndrome: report of a case and histopathologic analysis. 
  • Intratumoral consumption of indium-111 labeled platelets in a patient with hemangiomatosis and intravascular coagulation (Kasabach-Merritt syndrome). 
  • Iris vasculopathy in exfoliation syndrome. An immunocytochemical study. 
  • Is transplant operation important in determining posttransplant risk of bronchiolitis obliterans syndrome in lung transplant recipients? 
  • Jaffe-Campanacci syndrome. A case report and review of the literature. 
  • Jhum-jhum: neuropsychiatric symptoms in a Nepali village. 
  • Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene. 
  • Juvenile primary fibromyalgia syndrome. 
  • Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication? 
  • Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. 
  • LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. 
  • LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein. 
  • Lambert-Eaton myasthenic syndrome: the lack of short-term in vitro effects of serum factors on neuromuscular transmission. 
  • Lamotrigine in absence and primary generalized epilepsies. 
  • Laryngeal and ocular granulation tissue formation in two Punjabi children: LOGIC syndrome. 
  • Latest developments in the assessment and management of chronic musculoskeletal pain syndromes in children. 
  • Lessons learned from clinical trials in acute heart failure: phase 3 drug trials. 
  • Lifetime comorbidity, lifetime history of psychosis and suicide attempts, and current symptoms of patients with deteriorated affective disorder. 
  • Lithium carbonate in pseudobulbar palsy. 
  • Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. 
  • Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma. 
  • 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. 
  • 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. 
  • Longitudinal dimensionality of adolescent psychopathology: testing the differentiation hypothesis. 
  • Longitudinal study of neuropsychological functioning in patients on chronic hemodialysis: a preliminary report. 
  • 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. 
  • Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model. 
  • Man-in-the-barrel syndrome after thoracoilium fusion. 
  • 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. 
  • Management of severe lower abdominal or inguinal pain in high-performance athletes. PAIN (Performing Athletes with Abdominal or Inguinal Neuromuscular Pain Study Group). 
  • 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. 
  • Mesenteric Malperfusion Syndromes in Type A Aortic Dissection: Current Management Strategies. 
  • Mice lacking the p53-effector gene Gadd45a develop a lupus-like syndrome. 
  • Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome. 
  • Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients. 
  • Migraine. 
  • Minimally invasive colopexy for pediatric Chilaiditi syndrome. 
  • 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. 
  • 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. 
  • Molecular cross-talk among chromosome fragility syndromes. 
  • Mollaret meningitis. A report of three cases. 
  • Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA. 
  • Muir-Torre syndrome. 
  • Mullerian dysgenesis: a critical review of the literature. 
  • 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. 
  • Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A. 
  • Musculoskeletal syndromes associated with malignancy. 
  • Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. 
  • Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome. 
  • Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies. 
  • 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. 
  • Myoclonus and tremor response to thalamic deep brain stimulation parameters in a patient with inherited myoclonus-dystonia syndrome. 
  • Myopia predicts better outcome in persistent hyperplastic primary vitreous. 
  • Nager acrofacial dysostosis. 
  • National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines: clinical characteristics and utilization of biochemical markers in acute coronary syndromes. 
  • 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. 
  • Natural history of paclitaxel-associated acute pain syndrome: prospective cohort study NCCTG N08C1. 
  • 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. 
  • Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases. 
  • Neuroligins provide molecular links between syndromic and nonsyndromic autism. 
  • 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. 
  • Non-communicable disease syndemics: poverty, depression, and diabetes among low-income populations. 
  • Nonoperative and operative management of snapping scapula. 
  • Normative data for vascular and neurological tests of the hand-arm vibration syndrome. 
  • Novel approach to the treatment of distal malperfusion secondary to ascending aortic dissection. 
  • Occult spontaneous esophageal perforation. Unusual clinical and radiographic presentation. 
  • On angiomas of retina, brain, and skin. 
  • Optimal use of nitrogen to suppress the high pressure nervous syndrome. 
  • Oral platelet glycoprotein IIb/IIIa inhibition. 
  • 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). 
  • 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. 
  • Ovarian dysmetabolic syndrome. 
  • Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndrome. 
  • Overview of current noninodilator therapies for acute heart failure syndromes. 
  • PET Imaging of Dementia: Update 2022. 
  • PTEN loss in the continuum of common cancers, rare syndromes and mouse models. 
  • PURA Syndrome and Myotonia. 
  • Pain Syndromes and Management in Adult Hematopoietic Stem Cell Transplantation. 
  • Pain management strategies for thoracotomy and thoracic pain syndromes. 
  • Painful bone marrow edema syndrome of the foot and ankle. 
  • Pallister-Hall syndrome associated with an unbalanced chromosome translocation. 
  • Pan-aortic hybrid treatment of mega-aorta syndrome. 
  • Pancreatic insufficiency in Toriello-Carey syndrome: report of a second patient. 
  • Paraneoplastic limbic encephalopathy with testicular carcinoma. A reversible neurologic syndrome. 
  • Pathologic correlates of bronchiolitis obliterans syndrome in pulmonary retransplant recipients. 
  • Patterns of aspirin dosing in non-ST-elevation acute coronary syndromes in the CRUSADE Quality Improvement Initiative. 
  • Pediatric pain syndromes and management of pain in children and adolescents with rheumatic disease. 
  • Pediatric solid tumors and associated cancer predisposition syndromes: Workup, management, and surveillance. A summary from the APSA Cancer Committee. 
  • Pena-Shokeir type I syndrome: in utero sonographic appearance. 
  • 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. 
  • 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. 
  • Platelet activation in myocardial ischemic syndromes. 
  • Platypnea-Orthodeoxia Syndrome: To Shunt or Not to Shunt, That is the Question. 
  • 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. 
  • 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. 
  • 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. 
  • 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. 
  • Prediction of risk of death and myocardial infarction in the six months after presentation with acute coronary syndrome: prospective multinational observational study (GRACE). 
  • Predictors of target organ damage in hypertensive blacks and whites. 
  • 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. 
  • 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. 
  • 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. 
  • 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. 
  • 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. 
  • Pseudo-Mirizzi syndrome in acute cholecystitis. 
  • Pulmonary hemorrhage syndrome as a manifestation of disseminated intravascular coagulation: analysis of ten cases. 
  • Pulmonary hypertension and sleep apnea. 
  • Pulmonary hypertension associated with portal hypertension in a child with Williams syndrome--a case report. 
  • 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. 
  • Racial differences among high-risk patients presenting with non-ST-segment elevation acute coronary syndromes (results from the SYNERGY trial). 
  • 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. 
  • 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. 
  • Rapid remodeling of the maxillary sinus in silent sinus syndrome. 
  • Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. 
  • Rationale and clinical evidence for the use of GP IIb/IIIa inhibitors in acute coronary syndromes. 
  • Rationale and design of the GRACE (Global Registry of Acute Coronary Events) Project: a multinational registry of patients hospitalized with acute coronary syndromes. 
  • Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. 
  • Recurrent Hemispheric Stroke Syndromes in Symptomatic Atherosclerotic Internal Carotid Artery Occlusions: The Carotid Occlusion Surgery Study Randomized Trial. 
  • Red fingers syndrome in a patient with pseudolymphoma. 
  • Reflechi twòp--thinking too much: description of a cultural syndrome in Haiti's Central Plateau. 
  • Regional control after precision lymph node dissection for clinically evident melanoma metastasis. 
  • Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene. 
  • 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. 
  • Renal tubular insufficiency, cholestatic jaundice, and multiple congenital anomalies--a new multisystem syndrome. 
  • Resting-state functional connectivity predicts longitudinal pain symptom change in urologic chronic pelvic pain syndrome: a MAPP network study. 
  • Rheumatologic manifestations of cancer. 
  • Ring chromosome 17: phenotype variation by deletion size. 
  • Risk factors for ovarian cancers with and without microsatellite instability. 
  • Risk stratification in acute coronary syndromes: the need for continued vigilance in "low-risk" patients. 
  • ST-segment monitoring in patients with acute coronary syndromes. 
  • Sacral neuromodulation for the dysfunctional elimination syndrome: a single center experience with 20 children. 
  • 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. 
  • Screening for Moral Injury: The Moral Injury Symptom Scale - Military Version Short Form. 
  • Seckel syndrome and moyamoya. 
  • Seeking the optimal aspirin dose in acute coronary syndromes. 
  • Selective serotonin reuptake inhibitors for fibromyalgia syndrome. 
  • Self-discrepancies as predictors of vulnerability to distinct syndromes of chronic emotional distress. 
  • Self-healing juvenile cutaneous mucinosis. 
  • Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease. 
  • Serotonin-lesion myoclonic syndromes. I. Neurochemical profile and S-1 receptor binding. 
  • Severe laryngomalacia and bronchomalacia in DiGeorge syndrome and CHARGE association. 
  • Six-month outcomes of percutaneous coronary balloon angioplasty in acute coronary syndromes: Results from the PURSUIT trial. 
  • Solution structure of the NaV1.2 C-terminal EF-hand domain. 
  • Somnolence syndrome after focal radiation therapy to the pineal region: case report and review of the literature. 
  • Spatiotemporal changes in along-tract profilometry of cerebellar peduncles in cerebellar mutism syndrome. 
  • Spontaneous intracranial hemorrhage and multiple intracranial aneurysms in a patient with Roberts/SC phocomelia syndrome. 
  • Spontaneous intracranial hypotension syndrome treated with fludrocortisone. 
  • Statin therapy--time to turn the focus from efficacy to implementation? 
  • 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. 
  • Successful management of pain syndrome due to Angiostrongylus cantonensis by implantable spinal cord stimulator. 
  • Successful treatment of sudden hearing loss in Cogan's syndrome with corticosteroids. 
  • 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. 
  • Susac syndrome with transient inverted vision. 
  • Sustained ventricular arrhythmias among patients with acute coronary syndromes with no ST-segment elevation: incidence, predictors, and outcomes. 
  • Sweating in ectodermal dysplasia syndromes. A review. 
  • Symptom Clusters, Physical Activity, and Quality of Life: A Latent Class Analysis of Children During Maintenance Therapy for Leukemia. 
  • Symptom Management and Psychosocial Needs of Adults With Acute Myeloid Leukemia During Induction Treatment: A Pilot Study. 
  • Symptom Science: Advocating for Inclusion of Functional Genetic Polymorphisms. 
  • Symptom clusters in children. 
  • 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. 
  • Takotsubo cardiomyopathy: an unusual syndrome mimicking an ST-elevation myocardial infarction. 
  • Tapia's syndrome. The erratic evolution of an eponym. 
  • Temporal trends in the use of early cardiac catheterization in patients with non-ST-segment elevation acute coronary syndromes (results from CRUSADE). 
  • Tezosentan in patients with acute heart failure and acute coronary syndromes: design of the Randomized Intravenous Tezosentan study (RITZ-4). 
  • Tezosentan in patients with acute heart failure and acute coronary syndromes: results of the Randomized Intravenous TeZosentan Study (RITZ-4). 
  • The 'morning glory syndrome' - a mesodermal defect? 
  • The Editor's Roundtable: arterial thrombosis and acute coronary syndromes. 
  • 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. 
  • 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