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Orna Staretz Chacham

Showing results (11-20 of 49) with videos related to

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Genes|May 27, 2026
A Novel Variant in an Israeli Bedouin Family: The First Reported Cases of Carbonic Anhydrase VA (CA5A) Deficiency in IsraelNitzan Abelson, Eyal Kristal, Eli Hershkovitz, et al.
The Israel Medical Association Journal : IMAJ|July 17, 2009
Congenital diaphragmatic hernia: short-term outcomeShlomo Cohen-Katan, Nitza Newman-Heiman, Orna Staretz-Chacham, et al.
Genes|August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin TribeOrna Staretz-Chacham, Shirly Amar, Shlomo Almashanu, et al.
American Journal of Medical Genetics. Part A|December 12, 2017
A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansionIdan Cohen, Orna Staretz-Chacham, Ohad Wormser, et al.
Pediatric Pulmonology|July 17, 2025
Predischarge Betamethasone in Infants Diagnosed With Bronchopulmonary DysplasiaTal-El Ernest, Doreen Ozalvo, Orna Staretz-Chacham, 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|June 26, 2014
Early neonatal morbidities and associated modifiable and non-modifiable risk factors in a cohort of infants born at 34-35 weeks of gestationIris Morag, Avital L Okrent, Tzipora Strauss, et al.
Plos One|June 24, 2017
Inflammatory and vascular placental lesions are associated with neonatal amplitude integrated EEG recording in early premature neonatesDorit Paz-Levy, Letizia Schreiber, Offer Erez, et al.
Nutrients|October 23, 2021
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase DeficiencyOrna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, et al.
Molecular Genetics and Metabolism|April 9, 2011
A safety trial of high dose glyceryl triacetate for Canavan diseaseReeval Segel, Yair Anikster, Shoshana Zevin, et al.
Molecular Genetics & Genomic Medicine|February 13, 2020
A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiencyOrna Staretz-Chacham, Lars Schlotawa, Ohad Wormser, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Genes|May 27, 2026
A Novel Variant in an Israeli Bedouin Family: The First Reported Cases of Carbonic Anhydrase VA (CA5A) Deficiency in IsraelNitzan Abelson, Eyal Kristal, Eli Hershkovitz, et al.
The Israel Medical Association Journal : IMAJ|July 17, 2009
Congenital diaphragmatic hernia: short-term outcomeShlomo Cohen-Katan, Nitza Newman-Heiman, Orna Staretz-Chacham, et al.
Genes|August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin TribeOrna Staretz-Chacham, Shirly Amar, Shlomo Almashanu, et al.
American Journal of Medical Genetics. Part A|December 12, 2017
A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansionIdan Cohen, Orna Staretz-Chacham, Ohad Wormser, et al.
Pediatric Pulmonology|July 17, 2025
Predischarge Betamethasone in Infants Diagnosed With Bronchopulmonary DysplasiaTal-El Ernest, Doreen Ozalvo, Orna Staretz-Chacham, 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|June 26, 2014
Early neonatal morbidities and associated modifiable and non-modifiable risk factors in a cohort of infants born at 34-35 weeks of gestationIris Morag, Avital L Okrent, Tzipora Strauss, et al.
Plos One|June 24, 2017
Inflammatory and vascular placental lesions are associated with neonatal amplitude integrated EEG recording in early premature neonatesDorit Paz-Levy, Letizia Schreiber, Offer Erez, et al.
Nutrients|October 23, 2021
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase DeficiencyOrna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, et al.
Molecular Genetics and Metabolism|April 9, 2011
A safety trial of high dose glyceryl triacetate for Canavan diseaseReeval Segel, Yair Anikster, Shoshana Zevin, et al.
Molecular Genetics & Genomic Medicine|February 13, 2020
A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiencyOrna Staretz-Chacham, Lars Schlotawa, Ohad Wormser, et al.
Pageof 5