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Jose Bras

Showing results (31-40 of 118) with videos related to

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European Journal of Human Genetics : EJHG|December 3, 2020
Whole-exome sequencing of Finnish patients with vascular cognitive impairmentSaana Mönkäre, Liina Kuuluvainen, Celia Kun-Rodrigues, et al.
Human Molecular Genetics|October 17, 2008
Lack of replication of association between GIGYF2 variants and Parkinson diseaseJose Bras, Javier Simón-Sánchez, Monica Federoff, et al.
Neurobiology of Aging|December 28, 2007
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalJose Bras, Coro Paisan-Ruiz, Rita Guerreiro, et al.
European Journal of Neurology|January 12, 2022
Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypesMiguel Tábuas-Pereira, Isabel Santana, Maria Rosário Almeida, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2012
Hyposmia and cognitive impairment in Gaucher disease patients and carriersAlisdair McNeill, Raquel Duran, Christos Proukakis, et al.
American Journal of Human Genetics|March 3, 2015
Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4Jose Bras, Isabel Alonso, Clara Barbot, et al.
Neurobiology of Aging|December 14, 2011
Screening for VPS35 mutations in Parkinson's diseaseUna-Marie Sheerin, Gavin Charlesworth, Jose Bras, et al.
Neuro-Degenerative Diseases|September 7, 2013
Influence of single nucleotide polymorphisms in COMT, MAO-A and BDNF genes on dyskinesias and levodopa use in Parkinson's diseasePerdita Cheshire, Kelly Bertram, Helen Ling, et al.
BMC Neurology|January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
European Journal of Human Genetics : EJHG|February 25, 2018
Genetics of dementia in a Finnish cohortPetra Pasanen, Liisa Myllykangas, Minna Pöyhönen, et al.
Pageof 12

Showing results (31-40 of 118) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|December 3, 2020
Whole-exome sequencing of Finnish patients with vascular cognitive impairmentSaana Mönkäre, Liina Kuuluvainen, Celia Kun-Rodrigues, et al.
Human Molecular Genetics|October 17, 2008
Lack of replication of association between GIGYF2 variants and Parkinson diseaseJose Bras, Javier Simón-Sánchez, Monica Federoff, et al.
Neurobiology of Aging|December 28, 2007
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalJose Bras, Coro Paisan-Ruiz, Rita Guerreiro, et al.
European Journal of Neurology|January 12, 2022
Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypesMiguel Tábuas-Pereira, Isabel Santana, Maria Rosário Almeida, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2012
Hyposmia and cognitive impairment in Gaucher disease patients and carriersAlisdair McNeill, Raquel Duran, Christos Proukakis, et al.
American Journal of Human Genetics|March 3, 2015
Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4Jose Bras, Isabel Alonso, Clara Barbot, et al.
Neurobiology of Aging|December 14, 2011
Screening for VPS35 mutations in Parkinson's diseaseUna-Marie Sheerin, Gavin Charlesworth, Jose Bras, et al.
Neuro-Degenerative Diseases|September 7, 2013
Influence of single nucleotide polymorphisms in COMT, MAO-A and BDNF genes on dyskinesias and levodopa use in Parkinson's diseasePerdita Cheshire, Kelly Bertram, Helen Ling, et al.
BMC Neurology|January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
European Journal of Human Genetics : EJHG|February 25, 2018
Genetics of dementia in a Finnish cohortPetra Pasanen, Liisa Myllykangas, Minna Pöyhönen, et al.
Pageof 12