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Jose Bras

Showing results (61-70 of 118) with videos related to

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Neurobiology of Aging|October 26, 2016
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX arrayImelda S Barber, Anne Braae, Naomi Clement, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
American Journal of Human Genetics|December 4, 2012
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesisGavin Charlesworth, Vincent Plagnol, Kira M Holmström, et al.
Parkinsonism & Related Disorders|March 1, 2016
The clinical syndrome of dystonia with anarthria/aphoniaChristos Ganos, Belinda Crowe, Maria Stamelou, et al.
Brain : a Journal of Neurology|March 17, 2009
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseJuliane Neumann, Jose Bras, Emma Deas, et al.
JAMA Neurology|September 18, 2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosisIsabelle Le Ber, Agnès Camuzat, Rita Guerreiro, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Brain : a Journal of Neurology|January 9, 2022
Prion-like α-synuclein pathology in the brain of infants with Krabbe diseaseChristopher Hatton, Simona S Ghanem, David J Koss, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Neurobiology of Aging|January 25, 2016
Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's diseaseImelda S Barber, Jennyfer M García-Cárdenas, Chidchanok Sakdapanichkul, et al.
Pageof 12

Showing results (61-70 of 118) with videos related to

Sort By:
Pageof 12
Neurobiology of Aging|October 26, 2016
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX arrayImelda S Barber, Anne Braae, Naomi Clement, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
American Journal of Human Genetics|December 4, 2012
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesisGavin Charlesworth, Vincent Plagnol, Kira M Holmström, et al.
Parkinsonism & Related Disorders|March 1, 2016
The clinical syndrome of dystonia with anarthria/aphoniaChristos Ganos, Belinda Crowe, Maria Stamelou, et al.
Brain : a Journal of Neurology|March 17, 2009
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseJuliane Neumann, Jose Bras, Emma Deas, et al.
JAMA Neurology|September 18, 2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosisIsabelle Le Ber, Agnès Camuzat, Rita Guerreiro, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Brain : a Journal of Neurology|January 9, 2022
Prion-like α-synuclein pathology in the brain of infants with Krabbe diseaseChristopher Hatton, Simona S Ghanem, David J Koss, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Neurobiology of Aging|January 25, 2016
Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's diseaseImelda S Barber, Jennyfer M García-Cárdenas, Chidchanok Sakdapanichkul, et al.
Pageof 12