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Michal Inbar-Feigenberg

Showing results (1-10 of 47) with videos related to

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Molecular Genetics and Metabolism Reports|March 27, 2026
Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with MucopolysaccharidosisJian Dealy, Michal Inbar-Feigenberg
Molecular Genetics and Metabolism Reports|December 6, 2023
An unusually mild case of biotin-thiamine-responsive basal ganglia diseaseGurnoor Lail, Susan Blaser, Michal Inbar-Feigenberg
Ear, Nose, & Throat Journal|June 19, 2025
Early-Onset Hearing Loss in Leber's Hereditary Optic Neuropathy: A Case ReportMaria Al Bandari, Enas Nasr, Sharon L Cushing, et al.
Fertility and Sterility|January 30, 2013
Basic concepts of epigeneticsMichal Inbar-Feigenberg, Sanaa Choufani, Darci T Butcher, et al.
Paediatrics & Child Health|May 3, 2021
Ataxia and confusion in a 10-year-old girlCalvin C H Chan, Vinay Kukreti, Michal Inbar-Feigenberg, et al.
Metabolic Brain Disease|March 26, 2018
Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrestMichal Inbar-Feigenberg, Susan Blaser, Cynthia Hawkins, et al.
American Journal of Medical Genetics. Part A|September 6, 2025
Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5POZainab Al Masseri, Laura Guilder, Michal Inbar-Feigenberg, et al.
International Journal of Neonatal Screening|April 23, 2024
Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart ReviewMaria Al Bandari, Laura Nagy, Vivian Cruz, et al.
Molecular Genetics and Metabolism|June 6, 2021
Ultrasound findings of finger, wrist and knee joints in Mucopolysaccharidosis Type IJohannes Roth, Michal Inbar-Feigenberg, Julian Raiman, et al.
Molecular Genetics and Metabolism Reports|December 18, 2019
Use of waxy maize heat modified starch in the treatment of children between 2 and 5 years with glycogen storage disease type I: A retrospective studyGhada Hijazi, Nisha Pai, Laura L Nagy, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Molecular Genetics and Metabolism Reports|March 27, 2026
Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with MucopolysaccharidosisJian Dealy, Michal Inbar-Feigenberg
Molecular Genetics and Metabolism Reports|December 6, 2023
An unusually mild case of biotin-thiamine-responsive basal ganglia diseaseGurnoor Lail, Susan Blaser, Michal Inbar-Feigenberg
Ear, Nose, & Throat Journal|June 19, 2025
Early-Onset Hearing Loss in Leber's Hereditary Optic Neuropathy: A Case ReportMaria Al Bandari, Enas Nasr, Sharon L Cushing, et al.
Fertility and Sterility|January 30, 2013
Basic concepts of epigeneticsMichal Inbar-Feigenberg, Sanaa Choufani, Darci T Butcher, et al.
Paediatrics & Child Health|May 3, 2021
Ataxia and confusion in a 10-year-old girlCalvin C H Chan, Vinay Kukreti, Michal Inbar-Feigenberg, et al.
Metabolic Brain Disease|March 26, 2018
Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrestMichal Inbar-Feigenberg, Susan Blaser, Cynthia Hawkins, et al.
American Journal of Medical Genetics. Part A|September 6, 2025
Mitochondrial Complex V Deficiency Caused by a Homozygous Splice Variant in ATP5POZainab Al Masseri, Laura Guilder, Michal Inbar-Feigenberg, et al.
International Journal of Neonatal Screening|April 23, 2024
Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart ReviewMaria Al Bandari, Laura Nagy, Vivian Cruz, et al.
Molecular Genetics and Metabolism|June 6, 2021
Ultrasound findings of finger, wrist and knee joints in Mucopolysaccharidosis Type IJohannes Roth, Michal Inbar-Feigenberg, Julian Raiman, et al.
Molecular Genetics and Metabolism Reports|December 18, 2019
Use of waxy maize heat modified starch in the treatment of children between 2 and 5 years with glycogen storage disease type I: A retrospective studyGhada Hijazi, Nisha Pai, Laura L Nagy, et al.
Pageof 5