Alex V. Postma
www.medischebiologie.nl
0000-0003-4874-2487
103 papers found
Refreshing results…
A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14-p22
A new catecholaminergic polymorphic ventricular tachycardia-associated CASQ2 mutation causes hyperglycosylation, lower calcium binding, and defective sr calcium release
Molecular Cardiology
Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing.
Candidate genes for the hereditary component of cardiac hypertrophy:
A novel TBX5 mutation leads to enhanced DNA-binding in a family with Holt-Oram syndrome and paroxysmal atrial fibrillation
Heritability of left ventricular mass in a large cohort of twins. Commentary
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients
Catecholinergic ventricular tachycardia in children
Catecholinergic ventricular tachycardia in children,Tachycardies ventriculaires catécholergiques chez l'enfant.
Tachycardies ventriculaires catécholergiques chez l'enfant
Involvement of the Kir2 gene family in catecholaminergic polymorphic ventricular tachycardia; analysis for mutations and identification of numerous pseudogenes
Genetic aspects of cardiac arrythmia syndromes
Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia
RYR2 and CASQ2 mutations in catecholaminergic polymorphic ventricular
Catecholaminergic polymorphic ventricular tachycardia: A review
Ultrarapid Communication
Identification of 17 new mutations associated with catecholaminergic polymorphic ventricular tachycardia (CPVT) and their phenotypic variation
Age related and incomplete penetrance of the P4902S missense mutation of the cardiac ryanodine receptor gene in familial polymorphic ventricular tachycardia
Genetic heterogeneity of familial polymorphic ventricular tachycardia
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