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R L Carasso

Showing results (31-40 of 39) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1977
Measurement of prostaglandin E2 in cerebrospinal fluid in patients suffering from strokeR L Carasso, J Vardi, J M Rabay, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
Onset and progression of disease in familial and sporadic Parkinson's diseaseR Inzelberg, E Schecthman, D Paleacu, et al.
Neurology|January 3, 2001
Transient unilateral mydriasis as the presenting sign of aortic and carotid dissectionR Inzelberg, P Nisipeanu, S C Blumen, et al.
Neurology|October 26, 1999
Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin geneP Nisipeanu, R Inzelberg, S C Blumen, et al.
Neurology|April 23, 2003
Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutationR Inzelberg, N Hattori, P Nisipeanu, 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.
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 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1977
Measurement of prostaglandin E2 in cerebrospinal fluid in patients suffering from strokeR L Carasso, J Vardi, J M Rabay, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
Onset and progression of disease in familial and sporadic Parkinson's diseaseR Inzelberg, E Schecthman, D Paleacu, et al.
Neurology|January 3, 2001
Transient unilateral mydriasis as the presenting sign of aortic and carotid dissectionR Inzelberg, P Nisipeanu, S C Blumen, et al.
Neurology|October 26, 1999
Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin geneP Nisipeanu, R Inzelberg, S C Blumen, et al.
Neurology|April 23, 2003
Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutationR Inzelberg, N Hattori, P Nisipeanu, 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.
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