Z.A. Bhuiyan

Discipline

Psychologie (2) Gestion et management (2) Sociologie (1)

Type de document

Articles (18) Recensions (3)

Co-auteur

Date

Source

Mot-clé

mutation (10) Mutation (10) Patients (9) Arrhythmia (9) Patients (9) gène (8) Human beings (7) Families (7) Cardiac arrest (7) Long QT syndrome (7) maladie (6) Phenotype (6) Family (6) maladie (6) famille (5) âge (5) Treatment (5) Methods (5) Cases (5) Genes (5) Ventricular tachycardia (5) Age (5) Cases (5) Methods (5) Age (5) risque (4) analyse (4) Causes (4) Syndromes (4) Risk (4)

Documents écrit par Z.A. Bhuiyan (18) | parle de Z.A. Bhuiyan (0)

Editorial: Monogenic vs. Oligogenic Reclassification.
O. Messaoud et al. (2021)
Dysfonction sinusale, syndrome de Brugada et syndrome du QT long chez un même patient - Quand la génétique y perd son latin [Sinus node dysfunction, Brugada syndrome and long QT syndrome affecting the same patient : when genetics can't make head or tail of it]
A.P. Porretta et al. (3 juin 2020)
ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy.
J.M. Good et al.
Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.
A.M. Abdallah et al. (15 janv. 2019)
Genotype and clinical characteristics of congenital long QT syndrome in Thailand.
A. Saprungruang et al. (2018)
Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.
A.Y. Bdier et al.
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT.
H.D. Devalla et al.
Pheochromocytoma Masked by Mutation in the TH Gene.
K. Abid et al.
Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias.
M. Asadi et al.
Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia - a proof-of-concept study.
F. Maurer et al. (2016)
Sudden cardiac death in forensic medicine - Swiss recommendations for a multidisciplinary approach.
M. Wilhelm et al. (2015)
Sudden cardiac death among general population and sport related population in forensic experience.
N. Chappex et al. (2015)
Novel calmodulin mutations associated with congenital arrhythmia susceptibility.
N. Makita et al. (2014)
A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome.
S. Zumhagen et al. (2013)
Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia
Z.A. Bhuiyan et al. (2013)
Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia.
H. Watanabe et al. (2013)
Selective acquired long QT syndrome (saLQTS) upon risperidone treatment.
M.J. Lazarczyk et al. (2012)
Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene.
E. Nof et al. (2011)