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

I Gourfinkel-An

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Epilepsy and autism: a complex issue]C Amiet, I Gourfinkel-An, A Consoli, et al.
Dialogues in Clinical Neuroscience|October 29, 2011
Genetics of inherited human epilepsiesI Gourfinkel-An, S Baulac, A Brice, et al.
Revue Neurologique|July 23, 2004
[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]I Gourfinkel-An, S Baulac, R Nabbout, et al.
Journal of Inherited Metabolic Disease|October 25, 2007
Epilepsy and inborn errors of metabolism in adults: a diagnostic approachF Sedel, I Gourfinkel-An, O Lyon-Caen, et al.
Revue Neurologique|November 7, 2006
[Neurological manifestations of type 1 Gaucher's disease: Is a revision of disease classification needed?]P Chérin, F Sedel, C Mignot, et al.
Neurology|July 4, 2007
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin geneI Gourfinkel-An, C Duyckaerts, A Camuzat, et al.
Journal of Neurochemistry|September 3, 2003
Changes in GAD67 mRNA expression evidenced by in situ hybridization in the brain of R6/2 transgenic miceI Gourfinkel-An, K Parain, A Hartmann, et al.
Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
American Journal of Human Genetics|September 16, 1999
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33S Baulac, I Gourfinkel-An, F Picard, et al.
Nature Genetics|April 28, 2001
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit geneS Baulac, G Huberfeld, I Gourfinkel-An, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Epilepsy and autism: a complex issue]C Amiet, I Gourfinkel-An, A Consoli, et al.
Dialogues in Clinical Neuroscience|October 29, 2011
Genetics of inherited human epilepsiesI Gourfinkel-An, S Baulac, A Brice, et al.
Revue Neurologique|July 23, 2004
[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]I Gourfinkel-An, S Baulac, R Nabbout, et al.
Journal of Inherited Metabolic Disease|October 25, 2007
Epilepsy and inborn errors of metabolism in adults: a diagnostic approachF Sedel, I Gourfinkel-An, O Lyon-Caen, et al.
Revue Neurologique|November 7, 2006
[Neurological manifestations of type 1 Gaucher's disease: Is a revision of disease classification needed?]P Chérin, F Sedel, C Mignot, et al.
Neurology|July 4, 2007
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin geneI Gourfinkel-An, C Duyckaerts, A Camuzat, et al.
Journal of Neurochemistry|September 3, 2003
Changes in GAD67 mRNA expression evidenced by in situ hybridization in the brain of R6/2 transgenic miceI Gourfinkel-An, K Parain, A Hartmann, et al.
Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
American Journal of Human Genetics|September 16, 1999
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33S Baulac, I Gourfinkel-An, F Picard, et al.
Nature Genetics|April 28, 2001
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit geneS Baulac, G Huberfeld, I Gourfinkel-An, et al.
Pageof 2