Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrick A Dion

Showing results (51-60 of 188) with videos related to

Pageof 19
Sort By:
Neurobiology of Aging|November 16, 2010
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosisVéronique V Belzil, Hussein Daoud, Anne Desjarlais, et al.
European Journal of Medical Genetics|October 12, 2016
A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegiaMarina Diomedi, Ziv Gan-Or, Fabio Placidi, et al.
Pediatric Neurology|December 3, 2014
A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to painMaria Mansouri, Siham Chafai Elalaoui, Bouchra Ouled Amar Bencheikh, et al.
European Journal of Human Genetics : EJHG|July 21, 2022
The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosisKristiana Salmon, Jay P Ross, Vanessa Bertone, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 6, 2012
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjectsAnne Noreau, Patrick A Dion, Anna Szuto, et al.
Genome|November 19, 2013
Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorderCristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2006
Purification of the NF2 tumor suppressor protein from human erythrocytesHitesh K Jindal, Kazumi Yoshinaga, Pil-Soo Seo, et al.
Neurology. Genetics|September 21, 2016
GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysisVictoria Mallett, Jay P Ross, Roy N Alcalay, et al.
Neurobiology of Aging|February 4, 2017
RIC3 variants are not associated with Parkinson's disease in French-Canadians and FrenchJay P Ross, Nicolas Dupré, Yves Dauvilliers, et al.
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Pageof 19

Showing results (51-60 of 188) with videos related to

Sort By:
Pageof 19
Neurobiology of Aging|November 16, 2010
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosisVéronique V Belzil, Hussein Daoud, Anne Desjarlais, et al.
European Journal of Medical Genetics|October 12, 2016
A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegiaMarina Diomedi, Ziv Gan-Or, Fabio Placidi, et al.
Pediatric Neurology|December 3, 2014
A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to painMaria Mansouri, Siham Chafai Elalaoui, Bouchra Ouled Amar Bencheikh, et al.
European Journal of Human Genetics : EJHG|July 21, 2022
The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosisKristiana Salmon, Jay P Ross, Vanessa Bertone, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 6, 2012
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjectsAnne Noreau, Patrick A Dion, Anna Szuto, et al.
Genome|November 19, 2013
Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorderCristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2006
Purification of the NF2 tumor suppressor protein from human erythrocytesHitesh K Jindal, Kazumi Yoshinaga, Pil-Soo Seo, et al.
Neurology. Genetics|September 21, 2016
GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysisVictoria Mallett, Jay P Ross, Roy N Alcalay, et al.
Neurobiology of Aging|February 4, 2017
RIC3 variants are not associated with Parkinson's disease in French-Canadians and FrenchJay P Ross, Nicolas Dupré, Yves Dauvilliers, et al.
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Pageof 19