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S C Blumen

Showing results (11-20 of 18) with videos related to

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Neurology|May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, M Sadeh, A D Korczyn, et al.
Neurology|June 13, 2001
Parkin gene causing benign autosomal recessive juvenile parkinsonismP Nisipeanu, R Inzelberg, S Abo Mouch, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in IsraelS C Blumen, P Nisipeanu, M Sadeh, et al.
Neurology|August 26, 2009
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotesS C Blumen, J-P Bouchard, B Brais, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Annals of Neurology|July 13, 1999
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the diseaseS C Blumen, B Brais, A D Korczyn, et al.
Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
Nature Communications|April 1, 2017
PABPN1 gene therapy for oculopharyngeal muscular dystrophyA Malerba, P Klein, H Bachtarzi, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Neurology|May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, M Sadeh, A D Korczyn, et al.
Neurology|June 13, 2001
Parkin gene causing benign autosomal recessive juvenile parkinsonismP Nisipeanu, R Inzelberg, S Abo Mouch, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in IsraelS C Blumen, P Nisipeanu, M Sadeh, et al.
Neurology|August 26, 2009
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotesS C Blumen, J-P Bouchard, B Brais, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Annals of Neurology|July 13, 1999
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the diseaseS C Blumen, B Brais, A D Korczyn, et al.
Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
Nature Communications|April 1, 2017
PABPN1 gene therapy for oculopharyngeal muscular dystrophyA Malerba, P Klein, H Bachtarzi, et al.
Pageof 2