Search Results - "Gollob, M. H."
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Phospholamban cardiomyopathy: a Canadian perspective on a unique population
Published in Netherlands heart journal (01-04-2019)“…Introduction Phospholamban cardiomyopathy is an inherited cardiomyopathy, characterised by a defect in regulation of the sarcoplasmic reticulum Ca 2+ pump,…”
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2
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy
Published in Clinical genetics (01-05-2013)“…Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited myocardial disease that predominantly affects the right ventricle and is associated with…”
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3
Evolution of a genetic diagnosis
Published in Clinical genetics (01-12-2014)“…Understanding the relationship between genotype and phenotype has become an integral part of the diagnosis and management of patients with inherited…”
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4
Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome
Published in Biochemical Society transactions (01-02-2003)“…The AMP-activated protein kinase (AMPK) system was first discovered 30 years ago. Since that time, knowledge of the diverse physiological functions of AMPK has…”
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5
A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI study
Published in The pharmacogenomics journal (01-02-2016)“…Treatment of carriers of the CYP2C19*2 allele and ABCB1 TT genotype with clopidogrel is associated with increased ischemic complications after percutaneous…”
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6
Use of implantable cardioverter defibrillators in Canadian and US survivors of out-of-hospital cardiac arrest
Published in Canadian Medical Association journal (CMAJ) (03-07-2007)“…Cardiac arrest due to ventricular arrhythmia in the absence of a reversible cause or contraindication has been a class I indication for insertion of an…”
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AMP-activated protein kinase and familial Wolff–Parkinson–White syndrome: new perspectives on heart development and arrhythmogenesis
Published in European heart journal (01-05-2002)Get full text
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8
Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome
Published in The New England journal of medicine (14-06-2001)“…Probable causative mutation was identified in a protein kinase gene (PRKAG2) on chromosome 7. The Wolff–Parkinson–White syndrome is the second most common…”
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Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy
Published in Circulation (New York, N.Y.) (18-12-2001)“…We recently reported a mutation in the PRKAG2 gene to be responsible for a familial syndrome of ventricular preexcitation, atrial fibrillation, conduction…”
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10
Postradiation morphea
Published in Journal of rheumatology (01-11-1998)“…We describe a 54-year-old woman who developed right breast morphea after radiotherapy following a lumpectomy for infiltrating lobular carcinoma. Skin biopsy…”
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11
Current status of the implantable cardioverter-defibrillator
Published in Chest (01-04-2001)“…Clinical trials have established the superiority of the implantable cardioverter-defibrillator (ICD) over antiarrhythmic drug therapy in survivors of sudden…”
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12
Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation
Published in The New England journal of medicine (22-06-2006)“…In 4 of 15 patients with idiopathic atrial fibrillation, four novel, heterozygous mutations in GJA5 — the gene for the gap-junction protein connexin 40 — were…”
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13
Accessory atrioventricular node with properties of a typical accessory pathway: anatomic-electrophysiologic correlation
Published in Journal of cardiovascular electrophysiology (01-08-2000)“…We report an accessory AV node producing ventricular preexcitation and comprising the retrograde limb of AV reentrant tachycardia (AVRT). A 66-year-old man…”
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14
Risk stratification for sudden death in heart failure
Published in Minerva cardioangiologica (01-06-2007)“…Clinical trials provide evidence that an empiric approach of implantable cardioverter-defibrillator (ICD) implantation in heart failure patients (ejection…”
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15
Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies
Published in Frontiers in pharmacology (01-01-2012)“…Voltage-gated sodium channels (VGSC) are multi-molecular protein complexes expressed in both excitable and non-excitable cells. They are primarily formed by a…”
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16
Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation
Published in Europace (London, England) (01-08-2010)“…Atrial fibrillation (AF), the most common sustained cardiac arrhythmia, is an important cause of morbidity and mortality. A genetic mutation in the NPPA gene,…”
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17
Frequency of Peripartum Cardiomyopathy
Published in The American journal of cardiology (15-06-2006)“…Reports from case series have estimated the incidence of peripartum cardiomyopathy (PC) at 1 case/1,485 live births to 1 case/15,000 live births and probable…”
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No long-term psychological morbidity living with an implantable cardioverter defibrillator under advisory: the Medtronic Marquis experience
Published in Europace (London, England) (01-01-2009)“…Aims It is unclear whether there is important psychological morbidity associated with living with an implantable cardioverter defibrillator (ICD) under…”
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19
Gain-of-function mutation of Na sub(v)1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing
Published in Biochemical and biophysical research communications (27-02-2009)“…Genetic mutations of the cardiac sodium channel (SCN5A) specific only to the phenotype of atrial fibrillation have recently been described. However, data on…”
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20
Ventricular tachycardia following tube thoracotomy
Published in Europace (London, England) (01-10-2010)“…Arrhythmias provoked by tube thoracotomy are a rare complication. We report a ventricular tachycardia after chest tube insertion for a device-related…”
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