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

Meriem Tazir

Showing results (21-30 of 51) with videos related to

Pageof 6
Sort By:
Journal of the Neurological Sciences|December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophiesStéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2025
Loss of ANK3 Function Causes a Recessive Neurodevelopmental Disorder with Cerebellar AtaxiaReza Maroofian, Giulia Spoto, Dalila Moualek, et al.
Parkinsonism & Related Disorders|October 12, 2010
LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohortSoreya Belarbi, Nassima Hecham, Suzanne Lesage, et al.
American Journal of Human Genetics|January 19, 2002
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouseAnnachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, et al.
Neurogenetics|August 18, 2021
NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Cecilia Altuzarra, Alain Verloes, et al.
Neurogenetics|July 31, 2007
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesNizar Elleuch, Naima Bouslam, Sylvain Hanein, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 25, 2010
Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiencyCatarina M Quinzii, Luis C López, Robert W Gilkerson, et al.
Molecular Genetics and Metabolism|October 23, 2015
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwideSylvia Stockler-Ipsiroglu, Delia Apatean, Roberta Battini, et al.
Neuroepidemiology|August 15, 2012
Multicenter transversal two-phase study to determine a national prevalence of epilepsy in AlgeriaDalila Moualek, Lamia Ali Pacha, Samira Abrouk, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolismTorunn Fiskerstrand, Dorra H'mida-Ben Brahim, Stefan Johansson, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Journal of the Neurological Sciences|December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophiesStéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2025
Loss of ANK3 Function Causes a Recessive Neurodevelopmental Disorder with Cerebellar AtaxiaReza Maroofian, Giulia Spoto, Dalila Moualek, et al.
Parkinsonism & Related Disorders|October 12, 2010
LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohortSoreya Belarbi, Nassima Hecham, Suzanne Lesage, et al.
American Journal of Human Genetics|January 19, 2002
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouseAnnachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, et al.
Neurogenetics|August 18, 2021
NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Cecilia Altuzarra, Alain Verloes, et al.
Neurogenetics|July 31, 2007
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesNizar Elleuch, Naima Bouslam, Sylvain Hanein, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 25, 2010
Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiencyCatarina M Quinzii, Luis C López, Robert W Gilkerson, et al.
Molecular Genetics and Metabolism|October 23, 2015
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwideSylvia Stockler-Ipsiroglu, Delia Apatean, Roberta Battini, et al.
Neuroepidemiology|August 15, 2012
Multicenter transversal two-phase study to determine a national prevalence of epilepsy in AlgeriaDalila Moualek, Lamia Ali Pacha, Samira Abrouk, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolismTorunn Fiskerstrand, Dorra H'mida-Ben Brahim, Stefan Johansson, et al.
Pageof 6