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P Nisipeanu

Showing results (31-40 of 35) with videos related to

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Neurology|September 1, 1996
Double-blind comparison of cabergoline and bromocriptine in Parkinson's disease patients with motor fluctuationsR Inzelberg, P Nisipeanu, J M Rabey, 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|June 13, 2001
Parkin gene causing benign autosomal recessive juvenile parkinsonismP Nisipeanu, R Inzelberg, S Abo Mouch, 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 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Neurology|September 1, 1996
Double-blind comparison of cabergoline and bromocriptine in Parkinson's disease patients with motor fluctuationsR Inzelberg, P Nisipeanu, J M Rabey, 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|June 13, 2001
Parkin gene causing benign autosomal recessive juvenile parkinsonismP Nisipeanu, R Inzelberg, S Abo Mouch, 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 4