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A Brice

Showing results (71-80 of 353) with videos related to

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Muscle & Nerve|June 12, 1999
Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlationN Kubis, A Dürr, M Gugenheim, et al.
Annals of Neurology|July 14, 2000
D2 dopamine receptor gene in myoclonic dystonia and essential myoclonusA Dürr, J Tassin, M Vidailhet, et al.
Genomics|February 1, 1990
Localization of the choline acetyltransferase (CHAT) gene to human chromosome 10O Cohen-Haguenauer, A Brice, S Berrard, et al.
Environmental Science & Technology|December 14, 2007
Atmospheric atrazine at Canadian IADN sitesYuan Yao, Elisabeth Galarneau, Pierrette Blanchard, et al.
Nature Genetics|March 4, 2000
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?G Stevanin, A Herman, A Dürr, et al.
Journal of Neurology|October 20, 1999
Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3K Bürk, M Fetter, M Abele, et al.
La Revue De Medecine Interne|January 1, 1996
[Genetics of Alzheimer's disease]D Hannequin, D Campion, A Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 28, 2002
Parkin gene related neuronal multisystem disorderM W I M Horstink, B P C van de Warrenburg, M Lammens, et al.
Revue Neurologique|April 25, 2007
[Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)]I Feki, M I Miladi, N Elleuch, et al.
Neurology|May 9, 2001
A major locus for several phenotypes of myoclonus--dystonia on chromosome 7qM Vidailhet, J Tassin, F Durif, et al.
Pageof 36

Showing results (71-80 of 353) with videos related to

Sort By:
Pageof 36
Muscle & Nerve|June 12, 1999
Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlationN Kubis, A Dürr, M Gugenheim, et al.
Annals of Neurology|July 14, 2000
D2 dopamine receptor gene in myoclonic dystonia and essential myoclonusA Dürr, J Tassin, M Vidailhet, et al.
Genomics|February 1, 1990
Localization of the choline acetyltransferase (CHAT) gene to human chromosome 10O Cohen-Haguenauer, A Brice, S Berrard, et al.
Environmental Science & Technology|December 14, 2007
Atmospheric atrazine at Canadian IADN sitesYuan Yao, Elisabeth Galarneau, Pierrette Blanchard, et al.
Nature Genetics|March 4, 2000
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?G Stevanin, A Herman, A Dürr, et al.
Journal of Neurology|October 20, 1999
Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3K Bürk, M Fetter, M Abele, et al.
La Revue De Medecine Interne|January 1, 1996
[Genetics of Alzheimer's disease]D Hannequin, D Campion, A Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 28, 2002
Parkin gene related neuronal multisystem disorderM W I M Horstink, B P C van de Warrenburg, M Lammens, et al.
Revue Neurologique|April 25, 2007
[Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)]I Feki, M I Miladi, N Elleuch, et al.
Neurology|May 9, 2001
A major locus for several phenotypes of myoclonus--dystonia on chromosome 7qM Vidailhet, J Tassin, F Durif, et al.
Pageof 36