Gideon Eshel

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

Outbreak of Life-Threatening Thiamine Deficiency in Infants in Israel Caused by a Defective Soy-Based Formula

Aviva Fattal‐Valevski, Anat Kesler, Ben‐Ami Sela et al. · PEDIATRICS · 2005 · 192 citations

A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

Annick Raas‐Rothschild, Ronald J. A. Wanders, Petra A.W. Mooijer et al. · The American Journal of Human Genetics · 2002 · 71 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +9

Risk Factors Affecting the Immediate Postoperative Course in Pediatric Scoliosis Surgery

Roei Hod‐Feins, Ibrahim Abu‐Kishk, Gideon Eshel et al. · Spine · 2007 · 70 citations

Midazolam in treatment of epileptic seizures

Eli Lahat, Mordelhai Aladjem, Gideon Eshel et al. · Pediatric Neurology · 1992 · 56 citations

Epileptic Seizures, Neuropharmacology, Pharmacotherapy +4