Syndrome

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  Subject Areas on Research

  • A 29-year-old woman with sudden anemia and arterial oxygen desaturation. 
  • 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 combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). 
  • A conceptual model for the pathophysiology of vulvar vestibulitis syndrome. 
  • A fatal x-linked recessive reticuloendothelial syndrome with hyperglobulinemia. X-linked recessive reticuloendotheliosis. 
  • A model of neural cross-talk and irritation in the pelvis: implications for the overlap of chronic pelvic pain disorders. 
  • A national assessment of the epidemiology of severe fever with thrombocytopenia syndrome, China. 
  • 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 spatio-temporal absorbing state model for disease and syndromic surveillance. 
  • A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. 
  • 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 truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis. 
  • A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27. 
  • 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 2007 guidelines for the management of patients with unstable angina/non-ST-Elevation myocardial infarction: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 2002 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction) developed in collaboration with the American College of Emergency Physicians, the Society for Cardiovascular Angiography and Interventions, and the Society of Thoracic Surgeons endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation and the Society for Academic Emergency Medicine. 
  • ACC/AHA guidelines for the management of patients with unstable angina and non-ST segment elevation myocardial infarction: executive summary and recommendations. 
  • AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome. 
  • Abdominal migraine: prophylactic treatment and follow-up. 
  • 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? 
  • Absent pulmonary valve syndrome in infancy: surgery reconsidered. 
  • 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. 
  • 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. 
  • 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 Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficits. 
  • 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. 
  • Anti-Jo-1 syndrome presenting as cryptogenic organizing pneumonia. 
  • Anti-platelet factor 4/heparin antibodies: an independent predictor of 30-day myocardial infarction after acute coronary ischemic syndromes. 
  • Antibodies to platelet factor 4/heparin are associated with elevated endothelial cell activation markers in patients with acute coronary ischemic syndromes. 
  • 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. 
  • Antifibrinolytic therapy in the management of the Kasabach Merritt syndrome. 
  • Antigenic difference between viral strains causing classical and mild types of epidemic hemorrhagic fever with renal syndrome in China. 
  • Antiplatelet and antithrombin therapies in the acute coronary syndromes. 
  • Argon laser iridoplasty in the treatment of plateau-like iris configuration as result of numerous ciliary body cysts. 
  • Arthritis syndromes associated with human T cell lymphotropic virus type I infection. 
  • Arthrogryposis, renal tubular acidosis and cholestasis syndrome: spectrum of the clinical manifestations. 
  • Association between admission white blood cell count and one-year mortality in patients with acute coronary syndromes. 
  • 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. 
  • 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. 
  • 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. 
  • BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies. 
  • Biliary atresia-polysplenia syndrome: surgical and clinical relevance in liver transplantation. 
  • Binge eating disorder and night eating syndrome: psychological and behavioral characteristics. 
  • Bleeding events with abciximab in acute coronary syndromes without early revascularization: An analysis of GUSTO IV-ACS. 
  • Bleeding in acute coronary syndromes. 
  • Brief clinical report and review: the Marden-Walker syndrome. 
  • Bronchoalveolar lavage as a tool to predict, diagnose and understand bronchiolitis obliterans syndrome. 
  • CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290. 
  • CD7+, CD4-, CD8- acute leukemia: a syndrome of malignant pluripotent lymphohematopoietic cells. 
  • Cardiac markers in acute coronary syndromes-refining our knowledge. 
  • Cardiac rhabdomyosarcoma presenting as hypereosinophilic syndrome. 
  • Cases from the Osler Medical Service at Johns Hopkins University. Zieve syndrome. 
  • Celiac axis compression syndrome caused by sarcoidosis: an acquired form of the 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. 
  • Characteristics, treatment and outcome of patients with non-ST-elevation acute coronary syndromes and multivessel coronary artery disease: observations from PURSUIT (platelet glycoprotein IIb/IIIa in unstable angina: receptor suppression using integrelin therapy). 
  • Characterization of myocardial infarction as an end point in two large trials of acute coronary syndromes. 
  • Chest case of the day. Williams-Campbell syndrome. 
  • Chlamydia pneumoniae and acute chest syndrome in patients with sickle cell disease. 
  • Choanal atresia and associated anomalies. 
  • Choleduodenal fistula with gastric outlet obstruction. 
  • Chronic Lyme disease: the controversies and the science. 
  • Chronic ear surgery in patients with syndromes and multiple congenital malformations. 
  • Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal. 
  • Ciliary proteins and exencephaly. 
  • 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 and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. 
  • Clinical and molecular phenotype of Aicardi-Goutieres syndrome. 
  • 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 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. 
  • 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. 
  • Cogan's syndrome. 
  • 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. 
  • Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. 
  • 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? 
  • 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. 
  • Correlates of bleeding events among moderate- to high-risk patients undergoing percutaneous coronary intervention and treated with eptifibatide: observations from the PROTECT-TIMI-30 trial. 
  • Correlation between the international consensus definition of the Cancer Anorexia-Cachexia Syndrome (CACS) and patient-centered outcomes in advanced non-small cell lung cancer. 
  • Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease. 
  • Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease. 
  • Cryoablation of drug-resistant ventricular tachycardia in a patient with a variant of scleroderma. 
  • Cryosurgical ablation of accessory atrioventricular connections: a method for correction of the pre-excitation syndrome. 
  • Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhood. 
  • Cyclophosphamide therapy of severe systemic necrotizing vasculitis. 
  • 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 Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. 
  • 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. 
  • Development of a rapid whole blood flow cytometry procedure for the diagnosis of X-linked hyper-IgM syndrome patients and carriers. 
  • 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. 
  • Direct thrombin inhibitors in acute coronary syndromes: effect in patients undergoing early percutaneous coronary intervention. 
  • Distinct functions of Nijmegen breakage syndrome in ataxia telangiectasia mutated-dependent responses to DNA damage. 
  • 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. 
  • Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes. 
  • 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 angioplasty in acute coronary syndromes without persistent ST-segment elevation improves outcome but increases the need for six-month repeat revascularization: an analysis of the PURSUIT Trial. Platelet glycoprotein IIB/IIIA in Unstable angina: Receptor Suppression Using Integrilin Therapy. 
  • Early corneal findings in Cogan's syndrome. 
  • Early percutaneous coronary intervention, platelet inhibition with eptifibatide, and clinical outcomes in patients with acute coronary syndromes. PURSUIT Investigators. 
  • 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). 
  • 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. 
  • Endotoxemia associated with the Jarisch-Herxheimer reaction. 
  • Enteroviral meningoencephalitis as a complication of X-linked hyper IgM syndrome. 
  • Epidemiology of cardiorenal syndrome. 
  • Epidemiology of cardiorenal syndrome. 
  • Epilepsy in KCNH1-related syndromes. 
  • Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease. 
  • 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. 
  • 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. 
  • Evolution in cardiovascular care for elderly patients with non-ST-segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative. 
  • Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. 
  • Expanding CEP290 mutational spectrum in ciliopathies. 
  • Extent of ST-segment depression and cardiac events in non-ST-segment elevation acute coronary syndromes. 
  • Facilitatory effects of 4-aminopyridine on neuromuscular transmission in disease states. 
  • 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. 
  • 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. 
  • 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. 
  • Generalized epilepsies: emerging insights into cellular and genetic mechanisms. 
  • 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. 
  • Glutamate receptor autoimmunity in Rasmussen's encephalitis. 
  • Glycoprotein IIb/IIIa inhibitors in acute coronary syndromes: pathophysiologic foundation and clinical findings. 
  • HLA and Cogan's syndrome. 
  • Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiency. 
  • Health status, not head injury, predicts concussion symptoms after minor injury. 
  • 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. 
  • Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia. 
  • High incidence of pacemaker syndrome in patients with sinus node dysfunction treated with ventricular-based pacing in the Mode Selection Trial (MOST). 
  • 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. 
  • Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. 
  • IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena. 
  • 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. 
  • 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 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 postdischarge outcomes in patients hospitalized for acute heart failure syndromes. 
  • Improving the care of patients with non-ST-elevation acute coronary syndromes in the emergency department: the CRUSADE initiative. 
  • In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome. 
  • In search of the efficient way to medical decisions: the case of acute heart failure syndrome. 
  • Increased T follicular helper cells and germinal center B cells are required for cGVHD and bronchiolitis obliterans. 
  • Increasing evidence for syndromic phenotypes associated with RPGR mutations. 
  • Infantile glaucoma associated with the Diamond-Blackfan syndrome. 
  • 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. 
  • Inpatient and follow-up cardiology care and mortality for acute coronary syndrome patients in the Veterans Health Administration. 
  • 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. 
  • Inter-regional differences in acute coronary syndrome trials. 
  • Interferon-gamma for delayed pulmonary toxicity syndrome resistant to steroids. 
  • Intraoperative floppy iris syndrome: report of a case and histopathologic analysis. 
  • Intraoral treatment of Eagle's syndrome. 
  • Intratumoral consumption of indium-111 labeled platelets in a patient with hemangiomatosis and intravascular coagulation (Kasabach-Merritt syndrome). 
  • Introduction: evidence to practice in acute coronary syndromes. 
  • Is transplant operation important in determining posttransplant risk of bronchiolitis obliterans syndrome in lung transplant recipients? 
  • Jhum-jhum: neuropsychiatric symptoms in a Nepali village. 
  • Joubert syndrome: a haplotype segregation strategy and exclusion of the zinc finger protein of cerebellum 1 (ZIC1) gene. 
  • 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? 
  • 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. 
  • Laser Therapy for Genitourinary Syndrome of Menopause. 
  • 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. 
  • Link between caudal regression and Vater syndromes. 
  • Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. 
  • 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. 
  • Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility. 
  • Low-molecular-weight heparins and glycoprotein IIb/IIIa inhibitors with percutaneous coronary intervention in acute coronary syndromes. 
  • Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome. 
  • Lung transplantation for Williams-Campbell syndrome. 
  • Lymphedema in Noonan's syndrome. 
  • MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. 
  • 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). 
  • 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. 
  • Meta-analysis of cardiovascular outcomes trials comparing intensive versus moderate statin therapy. 
  • Meta-analysis of ischemia-modified albumin to rule out acute coronary syndromes in the emergency department. 
  • 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. 
  • 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 characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl. 
  • Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. 
  • Molecular cross-talk among chromosome fragility syndromes. 
  • Mollaret meningitis. A report of three cases. 
  • 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 types of immune complexes in patients with mixed cryoglobulinemia. 
  • Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. 
  • Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene. 
  • Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome. 
  • Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. 
  • Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. 
  • Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. 
  • Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. 
  • 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. 
  • National and regional registries: what good are they? 
  • Natriuretic peptides in heart failure with preserved ejection fraction. 
  • 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. 
  • Necrotizing lymphoid vasculitis in X-linked lymphoproliferative syndrome. 
  • Need for centers to care for patients with acute coronary syndromes. 
  • Neural misdirection in congenital ocular fibrosis syndrome: implications and pathogenesis. 
  • Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases. 
  • Neuroligins provide molecular links between syndromic and nonsyndromic autism. 
  • New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma. 
  • Non-ST segment elevation acute coronary syndromes: A comprehensive review. 
  • Non-communicable disease syndemics: poverty, depression, and diabetes among low-income populations. 
  • Nonoperative and operative management of snapping scapula. 
  • 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. 
  • Optimizing glycoprotein IIb/IIIa receptor antagonist use for the non-ST-segment elevation acute coronary syndromes: risk stratification and therapeutic intervention. 
  • Oral platelet glycoprotein IIb/IIIa inhibition. 
  • Outcomes after acute coronary syndrome admission to primary versus tertiary Veterans Affairs medical centers: the Veterans Affairs Access to Cardiology study. 
  • 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. 
  • Pain Syndromes and Management in Adult Hematopoietic Stem Cell Transplantation. 
  • Pain management strategies for thoracotomy and thoracic pain syndromes. 
  • 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. 
  • Patients with acute coronary syndromes without persistent ST elevation undergoing percutaneous coronary intervention benefit most from early intervention with protection by a glycoprotein IIb/IIIa receptor blocker. 
  • 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. 
  • Pena-Shokeir type I syndrome: in utero sonographic appearance. 
  • Percutaneous coronary interventions in patients with heparin-induced thrombocytopenia. 
  • Peripartum cardiomyopathy. A role for cardiac stress determinants other than pregnancy? 
  • Peripheral arterial disease, acute coronary syndromes, and early invasive management: the TACTICS TIMI 18 trial. 
  • 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. 
  • Planar cell polarity acts through septins to control collective cell movement and ciliogenesis. 
  • Platelet activation in myocardial ischemic syndromes. 
  • Platelet glycoprotein IIb/IIIa blockade and outcome of cardiogenic shock complicating acute coronary syndromes without persistent ST-segment elevation. 
  • Platelet glycoprotein IIb/IIIa inhibitors reduce mortality in diabetic patients with non-ST-segment-elevation acute coronary syndromes. 
  • Platypnea-Orthodeoxia Syndrome: To Shunt or Not to Shunt, That is the Question. 
  • Pneumographic findings in the infantile autism syndrome. A correlation with temporal lobe disease. 
  • 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 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). 
  • Preleukemic syndromes and other syndromes predisposing to leukemia. 
  • Premenstrual tension syndrome: the development of research diagnostic criteria and new rating scales. 
  • 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. 
  • 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. 
  • Pseudo-Mirizzi syndrome in acute cholecystitis. 
  • Pulmonary hemorrhage syndrome as a manifestation of disseminated intravascular coagulation: analysis of ten cases. 
  • Pulmonary hypertension associated with portal hypertension in a child with Williams syndrome--a case report. 
  • 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. 
  • 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 de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome. 
  • Red fingers syndrome in a patient with pseudolymphoma. 
  • Reflechi twòp--thinking too much: description of a cultural syndrome in Haiti's Central Plateau. 
  • Relation between baseline risk and treatment decisions in non-ST elevation acute coronary syndromes: an examination of international practice patterns. 
  • 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. 
  • Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1. 
  • 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. 
  • Sneddon's syndrome with granulomatous leptomeningeal infiltration. 
  • 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. 
  • Static and progressive neuromuscular disease in a kindred. 
  • 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. 
  • Successful use of extracorporeal membrane oxygenation in the treatment of acute chest syndrome in a child with severe sickle cell anemia. 
  • 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. 
  • 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. 
  • Sylvian aqueduct syndrome as a sign of acute obstructive hydrocephalus in children. 
  • 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. 
  • 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 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 MAPP research network: a novel study of urologic chronic pelvic pain syndromes. 
  • The MAPP research network: design, patient characterization and operations. 
  • The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. 
  • The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert 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 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 evolving role of glycoprotein IIb/IIIa inhibitor therapy in contemporary care of acute coronary syndrome patients. 
  • The genetics of the J wave patterns. 
  • The hepatopulmonary syndrome: radiologic findings in 10 patients. 
  • The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. 
  • 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 influence of race on health status outcomes one year after an acute coronary syndrome. 
  • The intra-articular component of the subscapularis tendon: anatomic and histological correlation in reference to surgical release in patients with frozen-shoulder syndrome. 
  • The neural crest in cardiac congenital anomalies. 
  • 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 ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa. 
  • The ophthalmologic manifestations of the cardio-facio-cutaneous syndrome. 
  • The peeling skin syndrome. 
  • 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 syndrome of 5-fluorouracil cardiotoxicity. An elusive cardiopathy. 
  • The syndrome of frontal lobe epilepsy: characteristics and surgical management. 
  • The syndrome of hyperostosis and hyperphosphatemia. 
  • 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. 
  • Tirofiban therapy for patients with acute coronary syndromes and prior coronary artery bypass grafting in the PRISM-PLUS trial. 
  • 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 of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide. 
  • Treatment planning and biomechanics of distraction osteogenesis from an orthodontic perspective. 
  • Triggers of acute coronary syndromes. 
  • 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. 
  • 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. 
  • 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. 
  • 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). 
  • Usher syndrome: correlation between visual field size and maximal ERG response b-wave amplitude. 
  • 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. 
  • Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. 
  • Vascular morphogenesis: tales of two syndromes. 
  • Vasomotor instability in neonates with chromosome 22q11 deletion syndrome. 
  • 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 renal and cardiac insufficiencies intersect: is there a role for natriuretic peptide testing in the 'cardio-renal syndrome'? 
  • When you hear hoof beats...do not forget the zebras. 
  • Women's Ischemic Syndrome Evaluation: current status and future research directions: report of the National Heart, Lung and Blood Institute workshop: October 2-4, 2002: Section 3: diagnosis and treatment of acute cardiac ischemia: gender issues. 
  • Women's health issues with fibromyalgia syndrome. 
  • X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. 
  • [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 B. Geller Professor for Research in Molecular Biology in the School of Medicine, Duke Cancer Institute
  • Cohen-Wolkowiez, Michael, Professor of Pediatrics, Pediatrics, Infectious Diseases
  • Davis, Erica Ellen, Associate Professor of Pediatrics, Cell Biology
  • Hoang, Jenny K., Associate Professor of Radiology, Radiology, Neuroradiology
  • Laskowitz, Daniel Todd, Professor of Neurology, Duke Innovation & Entrepreneurship
  • O'Connor, Christopher Michael, Richard Sean Stack, M.D. / Guidant Foundation Professor of Cardiology, Medicine, Clinical Pharmacology
  • Pitt, Geoffrey Stuart, Adjunct Professor in the Department of Medicine, Medicine, Cardiology
  • Silver, Debra Lynn, Associate Professor of Molecular Genetics and Microbiology, Duke Science & Society
  • Starmer, Charles Franklin, Professor Emeritus of Computer Science, Computer Science
  • Taylor, Gregory Alan, Associate Professor in Medicine, Immunology
  • Turner, Dennis Alan, Professor of Neurosurgery, Biomedical Engineering
  • Yancy Jr., William Samuel, Associate Professor of Medicine, Medicine, General Internal Medicine