Aviva Levitas

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase

Aviva Levitas, Emad Muhammad, Gali Harel et al. · European Journal of Human Genetics · 2010 · 111 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Presentation, natural history, and outcome in children and adolescents with double orifice mitral valve

Eli Zalzstein, Robert M. Hamilton, Nili Zucker et al. · The American Journal of Cardiology · 2004 · 93 citations

Medicine, Cardiology, Pediatrics +13

B-Type Natriuretic Peptide and Cardiovascular Function in Young Children With Obstructive Sleep Apnea

Aviv Goldbart, Aviva Levitas, Sari Greenberg‐Dotan et al. · CHEST Journal · 2010 · 86 citations

Medicine, Pediatrics, Physiology +15

Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

Robert Wallerstein, Carol E. Anderson, Beverly N. Hay et al. · Journal of Medical Genetics · 1997 · 79 citations · Full text

Life Sciences, Genetics, Human Genetics +12

<i>PLEKHM2</i>mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

Emad Muhammad, Aviva Levitas, Sonia R. Singh et al. · Human Molecular Genetics · 2015 · 75 citations · Full text

Life Sciences, Cardiology, Genetics +17