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Jean Pouget

Showing results (61-70 of 113) with videos related to

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Brain : a Journal of Neurology|December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotypeCécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Magma (New York, N.Y.)|December 18, 2010
Motor cortical reorganization is present after a single attack of multiple sclerosis devoid of cortico-spinal dysfunctionAudrey Rico, Wafaa Zaaraoui, Jerome Franques, et al.
Annals of Neurology|June 23, 2015
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophyGodelieve Morel, Cécile Rouzier, Annabelle Chaussenot, et al.
Journal of the Peripheral Nervous System : JPNS|November 21, 2018
IqYmune® is an effective maintenance treatment for multifocal motor neuropathy: A randomised, double-blind, multi-center cross-over non-inferiority study vs Kiovig®-The LIME StudyJean-Marc Léger, Ousmane Alfa Cissé, Dario Cocito, et al.
Orphanet Journal of Rare Diseases|September 5, 2015
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose studyOle B Suhr, Teresa Coelho, Juan Buades, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Archives of Neurology|August 19, 2007
Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypesKarine Nguyen, Guillaume Bassez, Martin Krahn, et al.
Journal of Neurology|November 11, 2023
Clinical and genetic features of patients suffering from CMT4JSadia Beloribi-Djefaflia, Raul Juntas Morales, Farzad Fatehi, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathyVilma-Lotta Lehtokari, Katarina Pelin, Agnes Herczegfalvi, et al.
European Journal of Human Genetics : EJHG|November 26, 2009
New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?Mouna Barat-Houari, Karine Nguyen, Rafaëlle Bernard, et al.
Pageof 12

Showing results (61-70 of 113) with videos related to

Sort By:
Pageof 12
Brain : a Journal of Neurology|December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotypeCécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Magma (New York, N.Y.)|December 18, 2010
Motor cortical reorganization is present after a single attack of multiple sclerosis devoid of cortico-spinal dysfunctionAudrey Rico, Wafaa Zaaraoui, Jerome Franques, et al.
Annals of Neurology|June 23, 2015
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophyGodelieve Morel, Cécile Rouzier, Annabelle Chaussenot, et al.
Journal of the Peripheral Nervous System : JPNS|November 21, 2018
IqYmune® is an effective maintenance treatment for multifocal motor neuropathy: A randomised, double-blind, multi-center cross-over non-inferiority study vs Kiovig®-The LIME StudyJean-Marc Léger, Ousmane Alfa Cissé, Dario Cocito, et al.
Orphanet Journal of Rare Diseases|September 5, 2015
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose studyOle B Suhr, Teresa Coelho, Juan Buades, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Archives of Neurology|August 19, 2007
Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypesKarine Nguyen, Guillaume Bassez, Martin Krahn, et al.
Journal of Neurology|November 11, 2023
Clinical and genetic features of patients suffering from CMT4JSadia Beloribi-Djefaflia, Raul Juntas Morales, Farzad Fatehi, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathyVilma-Lotta Lehtokari, Katarina Pelin, Agnes Herczegfalvi, et al.
European Journal of Human Genetics : EJHG|November 26, 2009
New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?Mouna Barat-Houari, Karine Nguyen, Rafaëlle Bernard, et al.
Pageof 12