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

P Bouche

Showing results (101-110 of 158) with videos related to

Pageof 16
Sort By:
European Neurology|January 1, 1988
Postradiation segmental myoclonus selectively inhibited by REM sleep (sleep-wake myoclonus)J J Askenasy, P Brunet, J M Leger, et al.
Muscle & Nerve|January 14, 1998
Peripheral neuropathy associated with IgM monoclonal gammopathy: correlations between M-protein antibody activity and clinical/electrophysiological features in 40 casesB Chassande, J M Léger, A B Younes-Chennoufi, et al.
Revue Neurologique|January 1, 1993
[4 new cases of neuromyositis, one of them associated with HTLV-I infection]R Laraki, O Bletry, G Raguin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Human immunoglobulin treatment of multifocal motor neuropathy and polyneuropathy associated with monoclonal gammopathyJ M Leger, A B Younes-Chennoufi, B Chassande, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 2007
Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis?K Viala, A Béhin, T Maisonobe, et al.
Muscle & Nerve|September 1, 1997
Recurrent polyradiculoneuropathy with the 17p11.2 deletionN Le Forestier, E LeGuern, P Coullin, et al.
Journal of Medical Genetics|June 1, 1997
SMN gene analysis of the spinal form of Charcot-Marie-Tooth diseaseA Hanash, E Leguern, N Birouk, et al.
Neurology|May 5, 1999
Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletionP Mouton, S Tardieu, R Gouider, et al.
American Journal of Human Genetics|March 1, 1996
High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patientsH Rouger, E LeGuern, R Gouider, et al.
Neurology|June 1, 1997
Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous systemL Magy, N Birouk, J M Vallat, et al.
Pageof 16

Showing results (101-110 of 158) with videos related to

Sort By:
Pageof 16
European Neurology|January 1, 1988
Postradiation segmental myoclonus selectively inhibited by REM sleep (sleep-wake myoclonus)J J Askenasy, P Brunet, J M Leger, et al.
Muscle & Nerve|January 14, 1998
Peripheral neuropathy associated with IgM monoclonal gammopathy: correlations between M-protein antibody activity and clinical/electrophysiological features in 40 casesB Chassande, J M Léger, A B Younes-Chennoufi, et al.
Revue Neurologique|January 1, 1993
[4 new cases of neuromyositis, one of them associated with HTLV-I infection]R Laraki, O Bletry, G Raguin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Human immunoglobulin treatment of multifocal motor neuropathy and polyneuropathy associated with monoclonal gammopathyJ M Leger, A B Younes-Chennoufi, B Chassande, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 2007
Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis?K Viala, A Béhin, T Maisonobe, et al.
Muscle & Nerve|September 1, 1997
Recurrent polyradiculoneuropathy with the 17p11.2 deletionN Le Forestier, E LeGuern, P Coullin, et al.
Journal of Medical Genetics|June 1, 1997
SMN gene analysis of the spinal form of Charcot-Marie-Tooth diseaseA Hanash, E Leguern, N Birouk, et al.
Neurology|May 5, 1999
Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletionP Mouton, S Tardieu, R Gouider, et al.
American Journal of Human Genetics|March 1, 1996
High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patientsH Rouger, E LeGuern, R Gouider, et al.
Neurology|June 1, 1997
Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous systemL Magy, N Birouk, J M Vallat, et al.
Pageof 16