Concepedia

Author

Avraham Zeharia

Schneider Children's Medical Center

Also Known As

A Zeharia, A. Zeharia, Avraham Zeharia, Kwame Anyane-Yeboa

95

Publications

2.8K

Citations

33

H-Index

127

Concepts

All Affiliations

Schneider Children's Medical CenterTel Aviv UniversityRabin Medical CenterHadassah Medical CenterWolfson Medical Center
AZ

About

Avraham Zeharia is an author at Schneider Children's Medical Center specializing in medicine, pathology, and pediatrics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Health Sciences

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Education

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Engineering

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Natural Sciences

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Avraham Zeharia

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62

Publications

2.5K

Citations

32

H-Index

YearCitations

Acute Infantile Liver Failure Due to Mutations in the TRMU Gene

Avraham Zeharia, Avraham Shaag, Orit Pappo,

The American Journal of Human Genetics

2009

224

Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

Avraham Zeharia, Avraham Shaag, Riekelt H. Houtkooper,

The American Journal of Human Genetics

2008

216

Management of Nontuberculous Mycobacteria-Induced Cervical Lymphadenitis With Observation Alone

Avraham Zeharia, Tal Eidlitz‐Markus, Y. Cohen,

The Pediatric Infectious Disease Journal

2008

117

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,

The American Journal of Human Genetics

2012

101

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,

Journal of Child Neurology

2005

77

Clinical Presentations of Mitochondrial Cardiomyopathies

Dorit Lev, Andreea Nissenkorn, Esther Leshinsky‐Silver,

Pediatric Cardiology

2004

72

Mutations in <i>HAO1</i> encoding glycolate oxidase cause isolated glycolic aciduria

Yaacov Frishberg, Avraham Zeharia, Roman Lyakhovetsky,

Journal of Medical Genetics

2014

69

Multicenter long‐term follow‐up of children with idiopathic West syndrome: ACTH versus vigabatrin

S. Cohen‐Sadan, Uri Kramer, Bruria Ben‐Zeev,

European Journal of Neurology

2009

67

Neurologic Presentations of Mitochondrial Disorders

Andreea Nissenkorn, Avraham Zeharia, Dorit Lev,

Journal of Child Neurology

2000

67

Mitochondrial hepato-encephalopathy due to deficiency of QIL1/MIC13 (C19orf70), a MICOS complex subunit

Avraham Zeharia, Jonathan R. Friedman, Ana Tobar,

European Journal of Human Genetics

2016

60

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