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A Asherov

Showing results (1-10 of 10) with videos related to

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Neurology|May 1, 1996
A simple and efficient method for apolipoprotein E genotype determinationJ Chapman, J Estupiñan, A Asherov, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Clinical features of oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, P Nisipeanu, M Sadeh, et al.
Lancet (London, England)|October 14, 1995
Familial Alzheimer's disease associated with S182 codon 286 mutationJ Chapman, A Asherov, N Wang, et al.
Neurology|May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, M Sadeh, A D Korczyn, et al.
Digestive Diseases and Sciences|July 1, 1996
Esophageal smooth muscle dysfunction in oculopharyngeal muscular dystrophyE Tiomny, O Khilkevic, A D Korczyn, et al.
Alzheimer Disease and Associated Disorders|January 1, 1996
APOE-epsilon 4 in patients with Alzheimer disease and vascular dementiaT A Treves, N M Bornstein, J Chapman, 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.
Alzheimer Disease and Associated Disorders|April 16, 1998
Apolipoprotein E4 in Parkinson disease and dementia: new data and meta-analysis of published studiesR Inzelberg, J Chapman, T A Treves, 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.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Neurology|May 1, 1996
A simple and efficient method for apolipoprotein E genotype determinationJ Chapman, J Estupiñan, A Asherov, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Clinical features of oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, P Nisipeanu, M Sadeh, et al.
Lancet (London, England)|October 14, 1995
Familial Alzheimer's disease associated with S182 codon 286 mutationJ Chapman, A Asherov, N Wang, et al.
Neurology|May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara JewsS C Blumen, M Sadeh, A D Korczyn, et al.
Digestive Diseases and Sciences|July 1, 1996
Esophageal smooth muscle dysfunction in oculopharyngeal muscular dystrophyE Tiomny, O Khilkevic, A D Korczyn, et al.
Alzheimer Disease and Associated Disorders|January 1, 1996
APOE-epsilon 4 in patients with Alzheimer disease and vascular dementiaT A Treves, N M Bornstein, J Chapman, 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.
Alzheimer Disease and Associated Disorders|April 16, 1998
Apolipoprotein E4 in Parkinson disease and dementia: new data and meta-analysis of published studiesR Inzelberg, J Chapman, T A Treves, 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.
Pageof 1