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Menachem Sadeh

Showing results (41-50 of 69) with videos related to

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Journal of the Neurological Sciences|November 25, 2010
Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A geneRon Dabby, Menachem Sadeh, Ronit Gilad, et al.
The Israel Medical Association Journal : IMAJ|March 21, 2006
Asymptomatic or minimally symptomatic hyperCKemia: histopathologic correlatesRon Dabby, Menachem Sadeh, Oscar Herman, et al.
The Israel Medical Association Journal : IMAJ|February 16, 2012
Clinical, electrophysiologic and pathologic findings in 10 patients with myotonic dystrophy 2Ron Dabby, Menachem Sadeh, Oscar Herman, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
The Israel Medical Association Journal : IMAJ|December 18, 2012
Clinical and genetic findings in eight Israeli patients with transthyretin-associated familial amyloid polyneuropathyLior Leibou, Jacob Frand, Menachem Sadeh, et al.
Journal of the Neurological Sciences|March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositisRon Dabby, Menachem Sadeh, David Hilton-Jones, et al.
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.
Stroke|September 2, 2006
Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficitsAmir Oron, Uri Oron, Jieli Chen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 23, 2019
Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutationsIsabel Conceição, Thibaud Damy, Manuel Romero, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Journal of the Neurological Sciences|November 25, 2010
Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A geneRon Dabby, Menachem Sadeh, Ronit Gilad, et al.
The Israel Medical Association Journal : IMAJ|March 21, 2006
Asymptomatic or minimally symptomatic hyperCKemia: histopathologic correlatesRon Dabby, Menachem Sadeh, Oscar Herman, et al.
The Israel Medical Association Journal : IMAJ|February 16, 2012
Clinical, electrophysiologic and pathologic findings in 10 patients with myotonic dystrophy 2Ron Dabby, Menachem Sadeh, Oscar Herman, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
The Israel Medical Association Journal : IMAJ|December 18, 2012
Clinical and genetic findings in eight Israeli patients with transthyretin-associated familial amyloid polyneuropathyLior Leibou, Jacob Frand, Menachem Sadeh, et al.
Journal of the Neurological Sciences|March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositisRon Dabby, Menachem Sadeh, David Hilton-Jones, et al.
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.
Stroke|September 2, 2006
Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficitsAmir Oron, Uri Oron, Jieli Chen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 23, 2019
Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutationsIsabel Conceição, Thibaud Damy, Manuel Romero, et al.
Pageof 7