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E Seidman

Showing results (191-200 of 533) with videos related to

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Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|December 31, 1998
Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalitiesC I Berul, M E Christe, M J Aronovitz, et al.
The Journal of Clinical Investigation|September 1, 1990
Familial hypertrophic cardiomyopathy is a genetically heterogeneous diseaseS D Solomon, J A Jarcho, W McKenna, et al.
Circulation Research|July 30, 2005
N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activityLiqun Zou, Mei Shen, Michael Arad, et al.
The Journal of Clinical Investigation|January 26, 2008
Eya4-deficient mice are a model for heritable otitis mediaFrederic F S Depreux, Keith Darrow, David A Conner, et al.
Biochemical Pharmacology|August 12, 2023
Effect of pharmacological heart failure drugs and gene therapy on Danon's cardiomyopathyDor Yadin, Tali Guetta, Zachary Petrover, et al.
Kidney International|February 7, 1998
CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic ricketsC L Kelleher, V M Buckalew, E D Frederickson, et al.
Circulation|May 15, 1996
Missense mutation in the pore region of HERG causes familial long QT syndromeD W Benson, C A MacRae, M R Vesely, et al.
Hepatology (Baltimore, Md.)|September 1, 1984
Spinal cord paralysis following sclerotherapy for esophageal varicesE Seidman, A M Weber, C L Morin, et al.
Science (New York, N.Y.)|July 20, 1984
The structure of rat preproatrial natriuretic factor as defined by a complementary DNA cloneC E Seidman, A D Duby, E Choi, et al.
Journal of Cardiovascular Electrophysiology|September 3, 2010
Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutationRonny Alcalai, Hiroko Wakimoto, Michael Arad, et al.
Pageof 54

Showing results (191-200 of 533) with videos related to

Sort By:
Pageof 54
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|December 31, 1998
Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalitiesC I Berul, M E Christe, M J Aronovitz, et al.
The Journal of Clinical Investigation|September 1, 1990
Familial hypertrophic cardiomyopathy is a genetically heterogeneous diseaseS D Solomon, J A Jarcho, W McKenna, et al.
Circulation Research|July 30, 2005
N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activityLiqun Zou, Mei Shen, Michael Arad, et al.
The Journal of Clinical Investigation|January 26, 2008
Eya4-deficient mice are a model for heritable otitis mediaFrederic F S Depreux, Keith Darrow, David A Conner, et al.
Biochemical Pharmacology|August 12, 2023
Effect of pharmacological heart failure drugs and gene therapy on Danon's cardiomyopathyDor Yadin, Tali Guetta, Zachary Petrover, et al.
Kidney International|February 7, 1998
CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic ricketsC L Kelleher, V M Buckalew, E D Frederickson, et al.
Circulation|May 15, 1996
Missense mutation in the pore region of HERG causes familial long QT syndromeD W Benson, C A MacRae, M R Vesely, et al.
Hepatology (Baltimore, Md.)|September 1, 1984
Spinal cord paralysis following sclerotherapy for esophageal varicesE Seidman, A M Weber, C L Morin, et al.
Science (New York, N.Y.)|July 20, 1984
The structure of rat preproatrial natriuretic factor as defined by a complementary DNA cloneC E Seidman, A D Duby, E Choi, et al.
Journal of Cardiovascular Electrophysiology|September 3, 2010
Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutationRonny Alcalai, Hiroko Wakimoto, Michael Arad, et al.
Pageof 54