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Methods in Molecular Medicine
|
August 26, 2006
Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing
Alex V Postma, Zahurul A Bhuiyan, Hennie Bikker
Trends in Cardiovascular Medicine
|
December 27, 2014
Molecular insight into heart development and congenital heart disease: An update review from the Arab countries
Elhadi H Aburawi, Hanan E Aburawi, Keith M Bagnall, et al.
Journal of Forensic and Legal Medicine
|
September 8, 2015
Sudden cardiac death among general population and sport related population in forensic experience
Nina Chappex, Jürg Schlaepfer, Florence Fellmann, et al.
Frontiers in Pediatrics
|
January 9, 2014
Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia
Zahurul A Bhuiyan, Safar Al-Shahrani, Jumana Al-Aama, et al.
Clinical Genetics
|
October 16, 2013
De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome
J Y Al-Aama, S Al-Ghamdi, A Y Bdier, et al.
Revue Medicale Suisse
|
June 23, 2017
[Multidisciplinary cardiogenetic counselling]
Florence Fellmann, Xavier Jeanrenaud, Nicole Sekarski, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome
Zahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
The Journal of Physiology
|
October 29, 2005
Long-QT syndrome-related sodium channel mutations probed by the dynamic action potential clamp technique
Géza Berecki, Jan G Zegers, Zahurul A Bhuiyan, et al.
Indian Pacing and Electrophysiology Journal
|
July 24, 2018
Genotype and clinical characteristics of congenital long QT syndrome in Thailand
Ankavipar Saprungruang, Apichai Khongphatthanayothin, John Mauleekoonphairoj, et al.
Heart Rhythm
|
August 1, 2006
Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family
Prince J Kannankeril, Zahurul A Bhuiyan, Dawood Darbar, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Methods in Molecular Medicine
|
August 26, 2006
Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing
Alex V Postma, Zahurul A Bhuiyan, Hennie Bikker
Trends in Cardiovascular Medicine
|
December 27, 2014
Molecular insight into heart development and congenital heart disease: An update review from the Arab countries
Elhadi H Aburawi, Hanan E Aburawi, Keith M Bagnall, et al.
Journal of Forensic and Legal Medicine
|
September 8, 2015
Sudden cardiac death among general population and sport related population in forensic experience
Nina Chappex, Jürg Schlaepfer, Florence Fellmann, et al.
Frontiers in Pediatrics
|
January 9, 2014
Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia
Zahurul A Bhuiyan, Safar Al-Shahrani, Jumana Al-Aama, et al.
Clinical Genetics
|
October 16, 2013
De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome
J Y Al-Aama, S Al-Ghamdi, A Y Bdier, et al.
Revue Medicale Suisse
|
June 23, 2017
[Multidisciplinary cardiogenetic counselling]
Florence Fellmann, Xavier Jeanrenaud, Nicole Sekarski, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome
Zahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
The Journal of Physiology
|
October 29, 2005
Long-QT syndrome-related sodium channel mutations probed by the dynamic action potential clamp technique
Géza Berecki, Jan G Zegers, Zahurul A Bhuiyan, et al.
Indian Pacing and Electrophysiology Journal
|
July 24, 2018
Genotype and clinical characteristics of congenital long QT syndrome in Thailand
Ankavipar Saprungruang, Apichai Khongphatthanayothin, John Mauleekoonphairoj, et al.
Heart Rhythm
|
August 1, 2006
Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family
Prince J Kannankeril, Zahurul A Bhuiyan, Dawood Darbar, et al.
Page
of 5