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Neuromuscular Disorders : NMD
|
December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel
S 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 disease
Y Neumann, A Toren, G Rechavi, et al.
Human Heredity
|
November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes
M M Menold, M Sadeh, F Lennon, et al.
Pediatric Cardiology
|
June 9, 2004
Clinical presentations of mitochondrial cardiomyopathies
D 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 dyskinesia
A 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 features
Z 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 dystonia
Y 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 2B
R 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 myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 119) with videos related to
Sort By:
Page
of 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 Israel
S 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 disease
Y Neumann, A Toren, G Rechavi, et al.
Human Heredity
|
November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes
M M Menold, M Sadeh, F Lennon, et al.
Pediatric Cardiology
|
June 9, 2004
Clinical presentations of mitochondrial cardiomyopathies
D 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 dyskinesia
A 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 features
Z 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 dystonia
Y 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 2B
R 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 myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Page
of 12