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A Brice

Showing results (61-70 of 353) with videos related to

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Neurology|April 1, 1997
A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth diseaseM Kessali, R Zemmouri, A Guilbot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Autosomal dominant paroxysmal kinesigenic choreoathetosis: a clinical and genetic study of two familiesF Picard, J Tassin, M Vidailhet, et al.
Progress in Brain Research|January 1, 1990
Choline acetyltransferase: a molecular genetic approachJ Mallet, S Berrard, A Brice, et al.
American Journal of Ophthalmology Case Reports|December 11, 2025
Report of a case of nasal-type extranodal NK/T-cell lymphoma with ciliary body involvement and literature review of interleukin-10 and interleukin-6 in intraocular T-cell lymphomaMadeline S Louie, Nathan A Brice, Edmund Tsui, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1994
Familial Parkinson's disease and polymorphism at the CYP2D6 locusP Mazzetti, E Le Guern, A M Bonnet, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Human Mutation|June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's diseaseG Raux, R Gantier, C Martin, et al.
Acta Neurologica Scandinavica|March 26, 2011
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG geneJ Koht, G Stevanin, A Durr, et al.
Pageof 36

Showing results (61-70 of 353) with videos related to

Sort By:
Pageof 36
Neurology|April 1, 1997
A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth diseaseM Kessali, R Zemmouri, A Guilbot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Autosomal dominant paroxysmal kinesigenic choreoathetosis: a clinical and genetic study of two familiesF Picard, J Tassin, M Vidailhet, et al.
Progress in Brain Research|January 1, 1990
Choline acetyltransferase: a molecular genetic approachJ Mallet, S Berrard, A Brice, et al.
American Journal of Ophthalmology Case Reports|December 11, 2025
Report of a case of nasal-type extranodal NK/T-cell lymphoma with ciliary body involvement and literature review of interleukin-10 and interleukin-6 in intraocular T-cell lymphomaMadeline S Louie, Nathan A Brice, Edmund Tsui, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1994
Familial Parkinson's disease and polymorphism at the CYP2D6 locusP Mazzetti, E Le Guern, A M Bonnet, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Human Mutation|June 30, 2000
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's diseaseG Raux, R Gantier, C Martin, et al.
Acta Neurologica Scandinavica|March 26, 2011
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG geneJ Koht, G Stevanin, A Durr, et al.
Pageof 36