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Jose M Bras

Showing results (1-10 of 14) with videos related to

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Clinical Genetics|June 10, 2011
Exome sequencing in Parkinson's diseaseJose M Bras, A B Singleton
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locusCornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging|May 30, 2015
EIF4G1 mutations do not cause Parkinson's diseaseNoah Nichols, Jose M Bras, Dena G Hernandez, et al.
Movement Disorders Clinical Practice|October 27, 2018
Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 MutationJose M Bras, Rita J Guerreiro, James T H Teo, et al.
BMC Neurology|July 11, 2006
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohortRita J Guerreiro, Jose M Bras, Isabel Santana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2010
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia seriesJoyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?Roberto Erro, Joshua Hersheson, Christos Ganos, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Neurobiology of Aging|January 7, 2012
Tau acts as an independent genetic risk factor in pathologically proven PDGavin Charlesworth, Sonia Gandhi, Jose M Bras, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Clinical Genetics|June 10, 2011
Exome sequencing in Parkinson's diseaseJose M Bras, A B Singleton
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locusCornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging|May 30, 2015
EIF4G1 mutations do not cause Parkinson's diseaseNoah Nichols, Jose M Bras, Dena G Hernandez, et al.
Movement Disorders Clinical Practice|October 27, 2018
Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 MutationJose M Bras, Rita J Guerreiro, James T H Teo, et al.
BMC Neurology|July 11, 2006
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohortRita J Guerreiro, Jose M Bras, Isabel Santana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2010
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia seriesJoyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?Roberto Erro, Joshua Hersheson, Christos Ganos, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Neurobiology of Aging|January 7, 2012
Tau acts as an independent genetic risk factor in pathologically proven PDGavin Charlesworth, Sonia Gandhi, Jose M Bras, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Pageof 2