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M Sadeh

Showing results (111-120 of 119) with videos related to

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Neuromuscular Disorders : NMD|December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in IsraelS C Blumen, P Nisipeanu, M Sadeh, et al.
Medical and Pediatric Oncology|April 1, 1996
Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth diseaseY Neumann, A Toren, G Rechavi, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
Pediatric Cardiology|June 9, 2004
Clinical presentations of mitochondrial cardiomyopathiesD Lev, A Nissenkorn, E Leshinsky-Silver, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Botulinum toxin for the treatment of oro-facial-lingual-masticatory tardive dyskinesiaA Rapaport, M Sadeh, D Stein, et al.
Brain : a Journal of Neurology|May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic featuresZ Argov, M Sadeh, K Mazor, et al.
Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.
Pageof 12

Showing results (111-120 of 119) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 119 results.
Neuromuscular Disorders : NMD|December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in IsraelS C Blumen, P Nisipeanu, M Sadeh, et al.
Medical and Pediatric Oncology|April 1, 1996
Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth diseaseY Neumann, A Toren, G Rechavi, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
Pediatric Cardiology|June 9, 2004
Clinical presentations of mitochondrial cardiomyopathiesD Lev, A Nissenkorn, E Leshinsky-Silver, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Botulinum toxin for the treatment of oro-facial-lingual-masticatory tardive dyskinesiaA Rapaport, M Sadeh, D Stein, et al.
Brain : a Journal of Neurology|May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic featuresZ Argov, M Sadeh, K Mazor, et al.
Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.
Pageof 12