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Aviva Levitas

Showing results (31-40 of 36) with videos related to

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European Journal of Human Genetics : EJHG|June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenaseAviva Levitas, Emad Muhammad, Gali Harel, et al.
Human Molecular Genetics|October 15, 2015
PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompactionEmad Muhammad, Aviva Levitas, Sonia R Singh, et al.
European Heart Journal|August 18, 2005
Provocation of sudden heart rate oscillation with adenosine exposes abnormal QT responses in patients with long QT syndrome: a bedside test for diagnosing long QT syndromeSami Viskin, Raphael Rosso, Ori Rogowski, et al.
Plos Genetics|September 14, 2020
A Novel Recessive Mutation in SPEG Causes Early Onset Dilated CardiomyopathyAviva Levitas, Emad Muhammad, Yuan Zhang, et al.
Journal of Cardiovascular Translational Research|November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic CardiomyopathyTomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Circulation|September 25, 2024
Sacubitril/Valsartan in Pediatric Heart Failure (PANORAMA-HF): A Randomized, Multicenter, Double-Blind TrialRobert Shaddy, Michael Burch, Paul F Kantor, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
European Journal of Human Genetics : EJHG|June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenaseAviva Levitas, Emad Muhammad, Gali Harel, et al.
Human Molecular Genetics|October 15, 2015
PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompactionEmad Muhammad, Aviva Levitas, Sonia R Singh, et al.
European Heart Journal|August 18, 2005
Provocation of sudden heart rate oscillation with adenosine exposes abnormal QT responses in patients with long QT syndrome: a bedside test for diagnosing long QT syndromeSami Viskin, Raphael Rosso, Ori Rogowski, et al.
Plos Genetics|September 14, 2020
A Novel Recessive Mutation in SPEG Causes Early Onset Dilated CardiomyopathyAviva Levitas, Emad Muhammad, Yuan Zhang, et al.
Journal of Cardiovascular Translational Research|November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic CardiomyopathyTomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Circulation|September 25, 2024
Sacubitril/Valsartan in Pediatric Heart Failure (PANORAMA-HF): A Randomized, Multicenter, Double-Blind TrialRobert Shaddy, Michael Burch, Paul F Kantor, et al.
Pageof 4