Avraham Zeharia

Acute Infantile Liver Failure Due to Mutations in the TRMU Gene

Avraham Zeharia, Avraham Shaag, Orit Pappo et al. · The American Journal of Human Genetics · 2009 · 224 citations · Full text

Hepatology, Genetic Disorder, Liver Physiology +12

Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

Avraham Zeharia, Avraham Shaag, Riekelt H. Houtkooper et al. · The American Journal of Human Genetics · 2008 · 216 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

Management of Nontuberculous Mycobacteria-Induced Cervical Lymphadenitis With Observation Alone

Avraham Zeharia, Tal Eidlitz‐Markus, Y. Cohen et al. · The Pediatric Infectious Disease Journal · 2008 · 117 citations

Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1

Lina Basel‐Vanagaite, Noam Zevit, Adi Har Zahav et al. · The American Journal of Human Genetics · 2012 · 101 citations · Full text

Metabolic Syndrome, Mutated Gpd1, Metabolic Disorder +13

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene

Avraham Zeharia, Nathan Fischel‐Ghodsian, Kari Casas et al. · Journal of Child Neurology · 2005 · 77 citations