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R D Currier

Showing results (41-50 of 57) with videos related to

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The New England Journal of Medicine|May 19, 1977
Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typingJ F Jackson, R D Currier, P I Terasaki, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locusS H Subramony, J D Fratkin, B V Manyam, et al.
Archives of Neurology|September 1, 1971
Sexual seizuresR D Currier, S C Little, J F Suess, et al.
Neurology|July 26, 2000
A medullary syndrome characterized by wild arm ataxiaJ H Jaster, T W Smith, A M Gleckman, et al.
Annals of Neurology|August 1, 1987
Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophyS J Kish, R D Currier, L Schut, et al.
Archives of Neurology|February 1, 1990
Morphometric studies in dominant olivopontocerebellar atrophy. Comparison of cell losses with amino acid decreasesE M Bebin, J Bebin, R D Currier, et al.
Neurology|December 1, 1995
Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxiaJ D Schwankhaus, J E Parisi, W R Gulledge, et al.
American Journal of Medical Genetics|January 1, 1980
Linkage studies in spinocerebellar ataxia (SCA)N E Morton, J M Lalouel, J F Jackson, et al.
Neurology|July 1, 1996
Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1P J Vig, J D Fratkin, D Desaiah, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Linkage studies on glyoxalase I (GLO), pepsinogen (PG), spinocerebellar ataxia (SCA1), and HLAJ E Whittington, B J Keats, J F Jackson, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|May 19, 1977
Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typingJ F Jackson, R D Currier, P I Terasaki, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locusS H Subramony, J D Fratkin, B V Manyam, et al.
Archives of Neurology|September 1, 1971
Sexual seizuresR D Currier, S C Little, J F Suess, et al.
Neurology|July 26, 2000
A medullary syndrome characterized by wild arm ataxiaJ H Jaster, T W Smith, A M Gleckman, et al.
Annals of Neurology|August 1, 1987
Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophyS J Kish, R D Currier, L Schut, et al.
Archives of Neurology|February 1, 1990
Morphometric studies in dominant olivopontocerebellar atrophy. Comparison of cell losses with amino acid decreasesE M Bebin, J Bebin, R D Currier, et al.
Neurology|December 1, 1995
Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxiaJ D Schwankhaus, J E Parisi, W R Gulledge, et al.
American Journal of Medical Genetics|January 1, 1980
Linkage studies in spinocerebellar ataxia (SCA)N E Morton, J M Lalouel, J F Jackson, et al.
Neurology|July 1, 1996
Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1P J Vig, J D Fratkin, D Desaiah, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Linkage studies on glyoxalase I (GLO), pepsinogen (PG), spinocerebellar ataxia (SCA1), and HLAJ E Whittington, B J Keats, J F Jackson, et al.
Pageof 6