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M B Davis

Showing results (71-80 of 106) with videos related to

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Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Annals of the New York Academy of Sciences|December 10, 1999
A family with Friedreich ataxia and onion-bulb formations at sural nerve biopsyA A Barreira, W Marques Júnior, M G Sweeney, et al.
Archives of Surgery (Chicago, Ill. : 1960)|April 1, 1996
The crime of saving lives: the FDA, John Najarian, and Minnesota ALGW A Collins, R M Humphreys, M B Davis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 1998
Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansionM G Hanna, M B Davis, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.
Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 11P Giunti, H Houlden, C Gardner-Thorpe, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|November 2, 2004
Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3W Marques, M B Davis, P M Abou-Sleiman, et al.
Neurology|January 2, 2008
What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealedE Matthews, S V Tan, D Fialho, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Annals of the New York Academy of Sciences|December 10, 1999
A family with Friedreich ataxia and onion-bulb formations at sural nerve biopsyA A Barreira, W Marques Júnior, M G Sweeney, et al.
Archives of Surgery (Chicago, Ill. : 1960)|April 1, 1996
The crime of saving lives: the FDA, John Najarian, and Minnesota ALGW A Collins, R M Humphreys, M B Davis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 1998
Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansionM G Hanna, M B Davis, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.
Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 11P Giunti, H Houlden, C Gardner-Thorpe, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|November 2, 2004
Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3W Marques, M B Davis, P M Abou-Sleiman, et al.
Neurology|January 2, 2008
What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealedE Matthews, S V Tan, D Fialho, et al.
Pageof 11