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Patrick A Dion

Showing results (31-40 of 188) with videos related to

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Cerebellum & Ataxias|September 3, 2015
Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellumAnne Noreau, Philippe Beauchemin, Alexandre Dionne-Laporte, et al.
Sleep Medicine|January 10, 2017
Genetics of restless legs syndromeJuliane Winkelmann, Barbara Schormair, Lan Xiong, et al.
Archives of Neurology|January 18, 2012
Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosisVeronique V Belzil, Jean-Sébastien Langlais, Hussein Daoud, et al.
Neurobiology of Aging|October 16, 2012
Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patientsHussein Daoud, Sylvia Dobrzeniecka, William Camu, et al.
Neurology. Genetics|January 15, 2019
Screening of novel restless legs syndrome-associated genes in French-Canadian familiesFulya Akçimen, Dan Spiegelman, Alexandre Dionne-Laporte, et al.
European Journal of Human Genetics : EJHG|June 29, 2012
Genetic analysis of SIGMAR1 as a cause of familial ALS with dementiaVéronique V Belzil, Hussein Daoud, William Camu, et al.
JAMA Neurology|August 11, 2015
A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With ErythrokeratodermiaCynthia V Bourassa, Salmo Raskin, Sérgio Serafini, et al.
Parkinsonism & Related Disorders|May 13, 2015
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysisZiv Gan-Or, Claire S Leblond, Victoria Mallett, et al.
Plos Genetics|January 10, 2013
WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio)Valérie Bercier, Edna Brustein, Meijiang Liao, et al.
Neurogenetics|August 12, 2015
Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian familyAnne Noreau, Roberta La Piana, Camille Marcoux, et al.
Pageof 19

Showing results (31-40 of 188) with videos related to

Sort By:
Pageof 19
Cerebellum & Ataxias|September 3, 2015
Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellumAnne Noreau, Philippe Beauchemin, Alexandre Dionne-Laporte, et al.
Sleep Medicine|January 10, 2017
Genetics of restless legs syndromeJuliane Winkelmann, Barbara Schormair, Lan Xiong, et al.
Archives of Neurology|January 18, 2012
Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosisVeronique V Belzil, Jean-Sébastien Langlais, Hussein Daoud, et al.
Neurobiology of Aging|October 16, 2012
Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patientsHussein Daoud, Sylvia Dobrzeniecka, William Camu, et al.
Neurology. Genetics|January 15, 2019
Screening of novel restless legs syndrome-associated genes in French-Canadian familiesFulya Akçimen, Dan Spiegelman, Alexandre Dionne-Laporte, et al.
European Journal of Human Genetics : EJHG|June 29, 2012
Genetic analysis of SIGMAR1 as a cause of familial ALS with dementiaVéronique V Belzil, Hussein Daoud, William Camu, et al.
JAMA Neurology|August 11, 2015
A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With ErythrokeratodermiaCynthia V Bourassa, Salmo Raskin, Sérgio Serafini, et al.
Parkinsonism & Related Disorders|May 13, 2015
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysisZiv Gan-Or, Claire S Leblond, Victoria Mallett, et al.
Plos Genetics|January 10, 2013
WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio)Valérie Bercier, Edna Brustein, Meijiang Liao, et al.
Neurogenetics|August 12, 2015
Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian familyAnne Noreau, Roberta La Piana, Camille Marcoux, et al.
Pageof 19