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Zahir A. Bhuiyan

University of Amsterdam

22

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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

2011 Circulation
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study

2011 Circulation
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The Response of the QT Interval to the Brief Tachycardia Provoked by Standing A Bedside Test for Diagnosing Long QT Syndrome

2010 Journal of The Peripheral Nervous System
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The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome A Comprehensive Open Reading Frame Mutational Analysis

2009 Journal of Clinical Virology
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Letters regarding article by Coronel et al, "Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: A combined electrophysiological, genetic, histopathologic, and computational study" - Response

2006 Palliative Medicine
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Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing

2006 Journal of Inherited Metabolic Disease
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AB47-5: Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular cardiomyopathy in the Netherlands

2006 Heart Rhythm
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Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

2006 Journal of Inherited Metabolic Disease
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Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience

2006 PLOS Biology
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A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

2005 Journal of Molecular and Cellular Cardiology
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Citations (197)