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

R Gouider

Showing results (41-50 of 51) with videos related to

Pageof 6
Sort By:
Neuro-Ophthalmology (Aeolus Press)|March 7, 2025
Study of Eye Movements Abnormalities in EpilepsyS Mrabet, I Abdelkefi, I Sghaier, et al.
Revue Neurologique|May 15, 2022
Arabic adaptation of the Edinburgh cognitive and behavioural Amyotrophic lateral sclerosis screen (ECAS-AR)I Kacem, Y Abida, W Ferchichi, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Human Genetics|January 1, 1996
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)V Timmerman, A Löfgren, E Le Guern, et al.
European Journal of Neurology|January 20, 2006
A recommended treatment algorithm in relapsing multiple sclerosis: report of an international consensus meetingD Karussis, L D Biermann, S Bohlega, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
American Journal of Human Genetics|June 13, 1998
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onsetM D Lalioti, H S Scott, P Genton, et al.
Multiple Sclerosis and Related Disorders|January 21, 2024
Consensus recommendations for diagnosis and treatment of Multiple Sclerosis: 2023 revision of the MENACTRIMS guidelinesB Yamout, M Al-Jumah, M A Sahraian, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Neuro-Ophthalmology (Aeolus Press)|March 7, 2025
Study of Eye Movements Abnormalities in EpilepsyS Mrabet, I Abdelkefi, I Sghaier, et al.
Revue Neurologique|May 15, 2022
Arabic adaptation of the Edinburgh cognitive and behavioural Amyotrophic lateral sclerosis screen (ECAS-AR)I Kacem, Y Abida, W Ferchichi, et al.
Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Human Genetics|January 1, 1996
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)V Timmerman, A Löfgren, E Le Guern, et al.
European Journal of Neurology|January 20, 2006
A recommended treatment algorithm in relapsing multiple sclerosis: report of an international consensus meetingD Karussis, L D Biermann, S Bohlega, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
American Journal of Human Genetics|April 11, 2003
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.
American Journal of Human Genetics|June 13, 1998
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onsetM D Lalioti, H S Scott, P Genton, et al.
Multiple Sclerosis and Related Disorders|January 21, 2024
Consensus recommendations for diagnosis and treatment of Multiple Sclerosis: 2023 revision of the MENACTRIMS guidelinesB Yamout, M Al-Jumah, M A Sahraian, et al.
Pageof 6