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Menachem Sadeh

Showing results (61-70 of 69) with videos related to

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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.
Biochemical and Biophysical Research Communications|January 27, 2005
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutationIlan Salama, Stephan Hinderlich, Zipora Shlomai, et al.
The Israel Medical Association Journal : IMAJ|January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Human Mutation|December 24, 2002
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadricepsIris Eisenberg, Gil Grabov-Nardini, Hagit Hochner, et al.
Annals of Clinical and Translational Neurology|February 11, 2023
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic featuresAmir Dori, Michael Arad, Yishay Wasserstrum, et al.
Neuromuscular Disorders : NMD|December 28, 2016
Congenital myasthenic syndrome in Israel: Genetic and clinical characterizationSharon Aharoni, Menachem Sadeh, Yehuda Shapira, et al.
Journal of Neurology|July 22, 2015
Frequent misdiagnosis of adult polyglucosan body diseaseMark A Hellmann, Or Kakhlon, Ezekiel H Landau, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Archives of Neurology|April 13, 2005
Early clinical heterogeneity in choreoacanthocytosisAlexander Lossos, Carol Dobson-Stone, Anthony P Monaco, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
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.
Biochemical and Biophysical Research Communications|January 27, 2005
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutationIlan Salama, Stephan Hinderlich, Zipora Shlomai, et al.
The Israel Medical Association Journal : IMAJ|January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Human Mutation|December 24, 2002
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadricepsIris Eisenberg, Gil Grabov-Nardini, Hagit Hochner, et al.
Annals of Clinical and Translational Neurology|February 11, 2023
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic featuresAmir Dori, Michael Arad, Yishay Wasserstrum, et al.
Neuromuscular Disorders : NMD|December 28, 2016
Congenital myasthenic syndrome in Israel: Genetic and clinical characterizationSharon Aharoni, Menachem Sadeh, Yehuda Shapira, et al.
Journal of Neurology|July 22, 2015
Frequent misdiagnosis of adult polyglucosan body diseaseMark A Hellmann, Or Kakhlon, Ezekiel H Landau, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Archives of Neurology|April 13, 2005
Early clinical heterogeneity in choreoacanthocytosisAlexander Lossos, Carol Dobson-Stone, Anthony P Monaco, et al.
Pageof 7