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

N Birouk

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
Neuromuscular Disorders : NMD|June 19, 2001
The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocityO Dubourg, S Tardieu, N Birouk, et al.
American Journal of Human Genetics|June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research GroupJ Lopes, E LeGuern, R Gouider, et al.
Brain : a Journal of Neurology|September 26, 2001
Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth diseaseO Dubourg, S Tardieu, N Birouk, et al.
Revue Neurologique|April 9, 2002
[Acute meningomyelitis and polyradiculoneuritis disclosing systemic lupus erythematosus]O Mouti, H Harmouch, M El Alaoui Faris, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Revue Neurologique|April 25, 2007
[T-cell lymphoma revealed by a mononeuritis multiplex: case report and review of literature]M Rahmani, N Birouk, A Amarti, et al.
Journal of Medical Genetics|April 16, 1998
The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth diseaseF Meggouh, A Benomar, H Rouger, et al.
Revue Neurologique|April 19, 2003
[Acute Guillain-Barré-like polyradiculoneuritis revealing acute systemic lupus erythematosus: two case studies and review of the literature]E Aït Benhaddou, N Birouk, M El Alaoui-Faris, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1A Guilbot, N Ravisé, A Bouhouche, et al.
American Journal of Human Genetics|August 12, 1999
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3A Bouhouche, A Benomar, N Birouk, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|June 19, 2001
The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocityO Dubourg, S Tardieu, N Birouk, et al.
American Journal of Human Genetics|June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research GroupJ Lopes, E LeGuern, R Gouider, et al.
Brain : a Journal of Neurology|September 26, 2001
Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth diseaseO Dubourg, S Tardieu, N Birouk, et al.
Revue Neurologique|April 9, 2002
[Acute meningomyelitis and polyradiculoneuritis disclosing systemic lupus erythematosus]O Mouti, H Harmouch, M El Alaoui Faris, et al.
Brain : a Journal of Neurology|May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 casesN Birouk, R Gouider, E Le Guern, et al.
Revue Neurologique|April 25, 2007
[T-cell lymphoma revealed by a mononeuritis multiplex: case report and review of literature]M Rahmani, N Birouk, A Amarti, et al.
Journal of Medical Genetics|April 16, 1998
The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth diseaseF Meggouh, A Benomar, H Rouger, et al.
Revue Neurologique|April 19, 2003
[Acute Guillain-Barré-like polyradiculoneuritis revealing acute systemic lupus erythematosus: two case studies and review of the literature]E Aït Benhaddou, N Birouk, M El Alaoui-Faris, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1A Guilbot, N Ravisé, A Bouhouche, et al.
American Journal of Human Genetics|August 12, 1999
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3A Bouhouche, A Benomar, N Birouk, et al.
Pageof 4