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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 velocity
O 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 Group
J 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 disease
O 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 cases
N 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 disease
F 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 EGR1
A 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-q21.3
A Bouhouche, A Benomar, N Birouk, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 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 velocity
O 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 Group
J 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 disease
O 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 cases
N 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 disease
F 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 EGR1
A 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-q21.3
A Bouhouche, A Benomar, N Birouk, et al.
Page
of 4