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Journal of Muscle Research and Cell Motility
|
September 9, 2020
Molecular adaptation to calsequestrin 2 (CASQ2) point mutations leading to catecholaminergic polymorphic ventricular tachycardia (CPVT): comparative analysis of R33Q and D307H mutants
Giorgia Valle, Michael Arad, Pompeo Volpe
Current Problems in Cardiology
|
December 11, 2008
Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyond
Guy Katz, Michael Arad, Michael Eldar
The Israel Medical Association Journal : IMAJ
|
June 30, 2005
Genetic ideology of dilated cardiompathy
Michael Arad, Hadas Lahat, Dov Freimark
Harefuah
|
December 15, 2011
[Hospice for end-stage heart failure and its relevance to Israel]
Yael Potashnik-Peled, Michael Arad, Dov Freimark
Pharmacology & Therapeutics
|
August 23, 2015
Inherited cardiomyopathies--Novel therapies
Dror B Leviner, Edith Hochhauser, Michael Arad
Human Molecular Genetics
|
September 28, 2002
Phenotypic diversity in hypertrophic cardiomyopathy
Michael Arad, J G Seidman, Christine E Seidman
European Journal of Preventive Cardiology
|
February 8, 2017
Blood pressure dynamics during exercise rehabilitation in heart failure patients
Idan Hecht, Michael Arad, Dov Freimark, et al.
Molecular and Cellular Biochemistry
|
April 16, 2002
Modulation of cardiac A1-adenosine receptors in rats following treatment with agents affecting heart rate
Nissim Balas, Michael Arad, Babeth Rabinowitz, et al.
Circulation Research
|
March 3, 2007
AMP-activated protein kinase in the heart: role during health and disease
Michael Arad, Christine E Seidman, J G Seidman
Prostaglandins & Other Lipid Mediators
|
May 16, 2020
Therapeutic approaches to diabetic cardiomyopathy: Targeting the antioxidant pathway
Michael Arad, Maayan Waldman, Nader G Abraham, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 144) with videos related to
Sort By:
Page
of 15
Journal of Muscle Research and Cell Motility
|
September 9, 2020
Molecular adaptation to calsequestrin 2 (CASQ2) point mutations leading to catecholaminergic polymorphic ventricular tachycardia (CPVT): comparative analysis of R33Q and D307H mutants
Giorgia Valle, Michael Arad, Pompeo Volpe
Current Problems in Cardiology
|
December 11, 2008
Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyond
Guy Katz, Michael Arad, Michael Eldar
The Israel Medical Association Journal : IMAJ
|
June 30, 2005
Genetic ideology of dilated cardiompathy
Michael Arad, Hadas Lahat, Dov Freimark
Harefuah
|
December 15, 2011
[Hospice for end-stage heart failure and its relevance to Israel]
Yael Potashnik-Peled, Michael Arad, Dov Freimark
Pharmacology & Therapeutics
|
August 23, 2015
Inherited cardiomyopathies--Novel therapies
Dror B Leviner, Edith Hochhauser, Michael Arad
Human Molecular Genetics
|
September 28, 2002
Phenotypic diversity in hypertrophic cardiomyopathy
Michael Arad, J G Seidman, Christine E Seidman
European Journal of Preventive Cardiology
|
February 8, 2017
Blood pressure dynamics during exercise rehabilitation in heart failure patients
Idan Hecht, Michael Arad, Dov Freimark, et al.
Molecular and Cellular Biochemistry
|
April 16, 2002
Modulation of cardiac A1-adenosine receptors in rats following treatment with agents affecting heart rate
Nissim Balas, Michael Arad, Babeth Rabinowitz, et al.
Circulation Research
|
March 3, 2007
AMP-activated protein kinase in the heart: role during health and disease
Michael Arad, Christine E Seidman, J G Seidman
Prostaglandins & Other Lipid Mediators
|
May 16, 2020
Therapeutic approaches to diabetic cardiomyopathy: Targeting the antioxidant pathway
Michael Arad, Maayan Waldman, Nader G Abraham, et al.
Page
of 15