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Ron Dabby

Showing results (41-50 of 53) with videos related to

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The Israel Medical Association Journal : IMAJ|December 18, 2013
Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish populationMenachem Sadeh, Benjamin Glazer, Zohar Landau, et al.
Plos One|February 10, 2011
The proteomic profile of hereditary inclusion body myopathyIlan Sela, Irit Milman Krentsis, Zipora Shlomai, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Frontiers in Neurology|February 15, 2021
Age-Related Clinical Presentation of MOG-IgG Seropositivity in IsraelLivnat Brill, Esther Ganelin-Cohen, Ron Dabby, et al.
Molecular Genetics and Metabolism|May 22, 2012
McArdle disease: a novel mutation in Jewish families from the Caucasus regionYishai Haimi Cohen, Nechama Shalva, Tal Markus-Eidlitz, et al.
Journal of Receptor and Signal Transduction Research|December 17, 2014
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblastsAvi Harazi, Malka Chaouat, Zippora Shlomai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2011
Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutationLubov Blumkin, Arvid Suls, Tine Deconinck, et al.
BMC Medical Genetics|August 14, 2016
Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contractureMiora Feinstein-Linial, Massimo Buvoli, Ada Buvoli, et al.
Journal of Clinical Medicine|February 27, 2026
The Clinical, Histological, and Genetic Spectrum of <i>RYR1</i> Variants-A Multi-Center Israeli Cohort StudyMira Ginsberg, Marina Michelson, Sharon Aharoni, et al.
Muscle & Nerve|March 6, 2020
Small-fiber neuropathy associated with autoinflammatory syndromes in children and adolescentsIris Shinkarevsky Fleitman, Yoram Nevo, Liora Harel, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
The Israel Medical Association Journal : IMAJ|December 18, 2013
Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish populationMenachem Sadeh, Benjamin Glazer, Zohar Landau, et al.
Plos One|February 10, 2011
The proteomic profile of hereditary inclusion body myopathyIlan Sela, Irit Milman Krentsis, Zipora Shlomai, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Frontiers in Neurology|February 15, 2021
Age-Related Clinical Presentation of MOG-IgG Seropositivity in IsraelLivnat Brill, Esther Ganelin-Cohen, Ron Dabby, et al.
Molecular Genetics and Metabolism|May 22, 2012
McArdle disease: a novel mutation in Jewish families from the Caucasus regionYishai Haimi Cohen, Nechama Shalva, Tal Markus-Eidlitz, et al.
Journal of Receptor and Signal Transduction Research|December 17, 2014
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblastsAvi Harazi, Malka Chaouat, Zippora Shlomai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2011
Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutationLubov Blumkin, Arvid Suls, Tine Deconinck, et al.
BMC Medical Genetics|August 14, 2016
Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contractureMiora Feinstein-Linial, Massimo Buvoli, Ada Buvoli, et al.
Journal of Clinical Medicine|February 27, 2026
The Clinical, Histological, and Genetic Spectrum of <i>RYR1</i> Variants-A Multi-Center Israeli Cohort StudyMira Ginsberg, Marina Michelson, Sharon Aharoni, et al.
Muscle & Nerve|March 6, 2020
Small-fiber neuropathy associated with autoinflammatory syndromes in children and adolescentsIris Shinkarevsky Fleitman, Yoram Nevo, Liora Harel, et al.
Pageof 6