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Hadas Lahat

Showing results (1-10 of 13) with videos related to

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The Israel Medical Association Journal : IMAJ|January 9, 2003
Autosomal recessive catecholamine-induced polymorphic ventricular tachycardiaHadas Lahat, Michael Eldar
Circulation|January 29, 2003
RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardiaHadas Lahat, Elon Pras, Michael Eldar
Annals of Medicine|June 5, 2004
A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelHadas Lahat, Elon Pras, Michael Eldar
Experimental and Clinical Cardiology|August 4, 2009
Autosomal recessive catecholamine-induced polymorphic ventricular tachycardiaHadas Lahat, Elon Pras, Michael Eldar
The Israel Medical Association Journal : IMAJ|June 30, 2005
Genetic ideology of dilated cardiompathyMichael Arad, Hadas Lahat, Dov Freimark
Trends in Cardiovascular Medicine|May 7, 2003
A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardiaMichael Eldar, Elon Pras, Hadas Lahat
The American Journal of Cardiology|January 13, 2004
A novel form of familial bidirectional ventricular tachycardiaEyal Nof, Hadas Lahat, Naama Constantini, et al.
BMC Medical Genomics|May 14, 2016
Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencingMoran Gal, Khen Khermesh, Michal Barak, et al.
American Journal of Human Genetics|March 28, 2002
A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish familyEran Pras, Etgar Levy-Nissenbaum, Tangiz Bakhan, et al.
Circulation|July 25, 2007
Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardiaEyal Nof, David Luria, Dovrat Brass, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
The Israel Medical Association Journal : IMAJ|January 9, 2003
Autosomal recessive catecholamine-induced polymorphic ventricular tachycardiaHadas Lahat, Michael Eldar
Circulation|January 29, 2003
RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardiaHadas Lahat, Elon Pras, Michael Eldar
Annals of Medicine|June 5, 2004
A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelHadas Lahat, Elon Pras, Michael Eldar
Experimental and Clinical Cardiology|August 4, 2009
Autosomal recessive catecholamine-induced polymorphic ventricular tachycardiaHadas Lahat, Elon Pras, Michael Eldar
The Israel Medical Association Journal : IMAJ|June 30, 2005
Genetic ideology of dilated cardiompathyMichael Arad, Hadas Lahat, Dov Freimark
Trends in Cardiovascular Medicine|May 7, 2003
A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardiaMichael Eldar, Elon Pras, Hadas Lahat
The American Journal of Cardiology|January 13, 2004
A novel form of familial bidirectional ventricular tachycardiaEyal Nof, Hadas Lahat, Naama Constantini, et al.
BMC Medical Genomics|May 14, 2016
Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencingMoran Gal, Khen Khermesh, Michal Barak, et al.
American Journal of Human Genetics|March 28, 2002
A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish familyEran Pras, Etgar Levy-Nissenbaum, Tangiz Bakhan, et al.
Circulation|July 25, 2007
Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardiaEyal Nof, David Luria, Dovrat Brass, et al.
Pageof 2