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525301 to 525400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Reduction in density of transverse tubules and L-type Ca(2+) channels in canine tachycardia-induced heart failure.
The sinoatrial node, a heterogeneous pacemaker structure.
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.
Blockade of effects of smoked marijuana by the CB1-selective cannabinoid receptor antagonist SR141716.
Diabetic cardiovascular autonomic neuropathy.
Right ventricular dysplasia: a report of 24 adult cases.
Promotion of atrial fibrillation by heart failure in dogs: atrial remodeling of a different sort.
Factors influencing infarct size following experimental coronary artery occlusions.
Protein kinases C and D mediate agonist-dependent cardiac hypertrophy through nuclear export of histone deacetylase 5.
Calcineurin/NFAT coupling participates in pathological, but not physiological, cardiac hypertrophy.
Transient regenerative potential of the neonatal mouse heart.
Echocardiographic determination of left ventricular mass in man. Anatomic validation of the method.
Cardiac hypertrophy: the good, the bad, and the ugly.
Dysregulation of the TSC-mTOR pathway in human disease.
Class II histone deacetylases act as signal-responsive repressors of cardiac hypertrophy.
Obesity as an independent risk factor for cardiovascular disease: a 26-year follow-up of participants in the Framingham Heart Study.
The role of autophagy in cardiomyocytes in the basal state and in response to hemodynamic stress.
MicroRNA-133 controls cardiac hypertrophy.
Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro.
Genetics of cardiac arrhythmias.
A randomized comparison of atrial and dual-chamber pacing in 177 consecutive patients with sick sinus syndrome: echocardiographic and clinical outcome.
The many roles of histone deacetylases in development and physiology: implications for disease and therapy.
Methodology of head-up tilt testing in patients with unexplained syncope.
Endogenous RGS proteins modulate SA and AV nodal functions in isolated heart: implications for sick sinus syndrome and AV block.
Cardiac sodium channelopathies.
Regulation of cardiac hypertrophy by intracellular signalling pathways.
Next-generation association studies for complex traits.
Long-term pacing in sinus node disease: effects of stimulation mode on cardiovascular morbidity and mortality.
Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.
Bioartificial sinus node constructed via in vivo gene transfer of an engineered pacemaker HCN Channel reduces the dependence on electronic pacemaker in a sick-sinus syndrome model.
A calcineurin-dependent transcriptional pathway for cardiac hypertrophy.
Benefit of atrial pacing in sleep apnea syndrome.
Long-term follow-up of patients from a randomised trial of atrial versus ventricular pacing for sick-sinus syndrome.
Prospective randomised trial of atrial versus ventricular pacing in sick-sinus syndrome.
Mugdha P Kulkarni
Oxidized CaMKII causes cardiac sinus node dysfunction in mice.
Adverse effect of ventricular pacing on heart failure and atrial fibrillation among patients with normal baseline QRS duration in a clinical trial of pacemaker therapy for sinus node dysfunction.
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.
Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.
New insights into pacemaker activity: promoting understanding of sick sinus syndrome.
A rare variant in MYH6 is associated with high risk of sick sinus syndrome.
small short nose, long philtrum
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A).
Several common variants modulate heart rate, PR interval and QRS duration.
Effect of diet and smoking intervention on the incidence of coronary heart disease. Report from the Oslo Study Group of a randomised trial in healthy men.
Pathological changes in virus infections of the lower respiratory tract in children.
Predicting sudden death in the population: the Paris Prospective Study I.
An overview of randomized trials of rehabilitation with exercise after myocardial infarction.
Kir6.2 is required for adaptation to stress.
Increased left ventricular mass and hypertrophy are associated with increased risk for sudden death.
Right ventricular cardiomyopathy and sudden death in young people.
Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A.
Thrombosis and acute coronary-artery lesions in sudden cardiac ischemic death.
A clinical trial of the angiotensin-converting-enzyme inhibitor trandolapril in patients with left ventricular dysfunction after myocardial infarction. Trandolapril Cardiac Evaluation (TRACE) Study Group.
Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. The Cardiac Arrhythmia Suppression Trial (CAST) Investigators.
Increased protein kinase C activity and expression of Ca2+-sensitive isoforms in the failing human heart.
A comparison of enalapril with hydralazine-isosorbide dinitrate in the treatment of chronic congestive heart failure.
Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice.
Effect of metoprolol CR/XL in chronic heart failure: Metoprolol CR/XL Randomised Intervention Trial in Congestive Heart Failure (MERIT-HF)
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
Stress pathways and heart failure.
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
A mouse model of familial hypertrophic cardiomyopathy.
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction?
American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Europea...
Akt induces enhanced myocardial contractility and cell size in vivo in transgenic mice.
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles.
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Hypertrophic cardiomyopathy: a systematic review.
Phase II clinical trial of moderate hypothermia after severe traumatic brain injury in children.
Intensive care of patients with acute liver failure: recommendations of the U.S. Acute Liver Failure Study Group.
An outbreak of eosinophilic meningitis caused by Angiostrongylus cantonensis in travelers returning from the Caribbean.
A trial of intracranial-pressure monitoring in traumatic brain injury.
Pathophysiology of traumatic brain injury.
Traumatic brain injury.
Factors affecting excitatory amino acid release following severe human head injury.
Mechanisms of hyperbaric oxygen-induced neuroprotection in a rat model of subarachnoid hemorrhage.
Diagnosis and management of increased intracranial pressure in patients with AIDS and cryptococcal meningitis. The NIAID Mycoses Study Group and AIDS Cooperative Treatment Groups.
Insulin therapy protects the central and peripheral nervous system of intensive care patients.
Decompressive craniectomy in diffuse traumatic brain injury.
Diagnostic criteria for idiopathic intracranial hypertension.
Assessment of beta-amyloid in a frontal cortical brain biopsy specimen and by positron emission tomography with carbon 11-labeled Pittsburgh Compound B.
Amyloid-beta dynamics correlate with neurological status in the injured human brain.
Aquaporin-4 facilitates reabsorption of excess fluid in vasogenic brain edema.
Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of america.
Type 2 diabetes and atrophy of medial temporal lobe structures on brain MRI.
Endarterectomy versus stenting in patients with symptomatic severe carotid stenosis.
Association between carotid plaque characteristics and subsequent ischemic cerebrovascular events: a prospective assessment with MRI--initial results.
Expression of the elastolytic cathepsins S and K in human atheroma and regulation of their production in smooth muscle cells.
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Silent brain infarcts and white matter lesions increase stroke risk in the general population: the Rotterdam Scan Study.
Atherosclerotic lesion size and vulnerability are determined by patterns of fluid shear stress.
Statin therapy accelerates reendothelialization: a novel effect involving mobilization and incorporation of bone marrow-derived endothelial progenitor cells.
Expression of toll-like receptors in human atherosclerotic lesions: a possible pathway for plaque activation.
Protected carotid-artery stenting versus endarterectomy in high-risk patients.
Stenting versus endarterectomy for treatment of carotid-artery stenosis.