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Dorit Lev

Showing results (71-80 of 176) with videos related to

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Orphanet Journal of Rare Diseases|April 6, 2026
Elevated iron levels in tears of patients diagnosed with WDR45 X-linked optic atrophyMarina Michelson, Alon Zahavi, Tal Zobok, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 14, 2020
Isolated ventricular septal defects demonstrated by fetal echocardiography: prenatal course and postnatal outcomeAlona Raucher Sternfeld, Amichai Sheffy, Akiva Tamir, et al.
American Journal of Medical Genetics. Part A|March 21, 2022
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorderMarina Michelson, Gabriel Lidzbarsky, Daniella Nishri, et al.
European Journal of Medical Genetics|September 5, 2020
Myoclonic tremor status as a presenting symptom of adenylosuccinate lyase deficiencyMichal M Andelman-Gur, Hirotomo Saitsu, Naomichi Matsumoto, et al.
Metabolic Brain Disease|April 12, 2019
Metabolic stroke in a patient with bi-allelic OPA1 mutationsAyelet Zerem, Keren Yosovich, Yael Cohen Rappaport, et al.
Journal of Child Neurology|July 5, 2007
Acute intermittent porphyria, Rasmussen encephalitis, or both?Barak Tziperman, Ben-Zion Garty, Nili Schoenfeld, et al.
Clinical Immunology (Orlando, Fla.)|June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndromeIlan Dalal, Diana Tasher, Raz Somech, et al.
Journal of Child Neurology|May 4, 2019
Familial Intracranial Hypertension in 2 Brothers With <i>PTEN</i> Mutation: Expansion of the Phenotypic SpectrumRonen Hady-Cohen, Idit Maharshak, Marina Michelson, et al.
Human Mutation|March 17, 2004
Genetic and biochemical analyses of Israeli osteogenesis imperfecta patientsLiat Ries-Levavi, Tsofia Ish-Shalom, Moshe Frydman, et al.
Journal of Child Neurology|January 8, 2021
Congenital Mirror Movements Associated With Brain MalformationsAndreea Nissenkorn, Keren Yosovich, Zvi Leibovitz, et al.
Pageof 18

Showing results (71-80 of 176) with videos related to

Sort By:
Pageof 18
Orphanet Journal of Rare Diseases|April 6, 2026
Elevated iron levels in tears of patients diagnosed with WDR45 X-linked optic atrophyMarina Michelson, Alon Zahavi, Tal Zobok, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 14, 2020
Isolated ventricular septal defects demonstrated by fetal echocardiography: prenatal course and postnatal outcomeAlona Raucher Sternfeld, Amichai Sheffy, Akiva Tamir, et al.
American Journal of Medical Genetics. Part A|March 21, 2022
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorderMarina Michelson, Gabriel Lidzbarsky, Daniella Nishri, et al.
European Journal of Medical Genetics|September 5, 2020
Myoclonic tremor status as a presenting symptom of adenylosuccinate lyase deficiencyMichal M Andelman-Gur, Hirotomo Saitsu, Naomichi Matsumoto, et al.
Metabolic Brain Disease|April 12, 2019
Metabolic stroke in a patient with bi-allelic OPA1 mutationsAyelet Zerem, Keren Yosovich, Yael Cohen Rappaport, et al.
Journal of Child Neurology|July 5, 2007
Acute intermittent porphyria, Rasmussen encephalitis, or both?Barak Tziperman, Ben-Zion Garty, Nili Schoenfeld, et al.
Clinical Immunology (Orlando, Fla.)|June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndromeIlan Dalal, Diana Tasher, Raz Somech, et al.
Journal of Child Neurology|May 4, 2019
Familial Intracranial Hypertension in 2 Brothers With <i>PTEN</i> Mutation: Expansion of the Phenotypic SpectrumRonen Hady-Cohen, Idit Maharshak, Marina Michelson, et al.
Human Mutation|March 17, 2004
Genetic and biochemical analyses of Israeli osteogenesis imperfecta patientsLiat Ries-Levavi, Tsofia Ish-Shalom, Moshe Frydman, et al.
Journal of Child Neurology|January 8, 2021
Congenital Mirror Movements Associated With Brain MalformationsAndreea Nissenkorn, Keren Yosovich, Zvi Leibovitz, et al.
Pageof 18