Tova Hershkovitz

KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases

Felippe Borlot, Ahmed Abushama, Nadine Morrison‐Levy et al. · Epilepsia · 2020 · 85 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Biallelic SZT2 Mutations Cause Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum

Lina Basel‐Vanagaite, Tova Hershkovitz, Eli Heyman et al. · The American Journal of Human Genetics · 2013 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine

Alina Kurolap, Anja Armbruster, Tova Hershkovitz et al. · The American Journal of Human Genetics · 2016 · 40 citations · Full text

Life Sciences, Neurology, Neuroscience +11

A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome

Tova Hershkovitz, Gamal Hassoun, M. Indelman et al. · Clinical and Experimental Dermatology · 2006 · 35 citations

Life Sciences, Genetics, Molecular Genetics +17

Eculizumab Is Safe and Effective as a Long‐term Treatment for Protein‐losing Enteropathy Due to CD55 Deficiency

Alina Kurolap, Orly Eshach Adiv, Tova Hershkovitz et al. · Journal of Pediatric Gastroenterology and Nutrition · 2018 · 34 citations

Medicine, Pharmacology, Pharmacotherapy +17