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N Birouk

Showing results (11-20 of 36) with videos related to

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Revue Neurologique|October 17, 1998
[Pure motor neuropathy after radiation therapy: 6 cases]T Lalu, B Mercier, N Birouk, et al.
Annales De Dermatologie Et De Venereologie|October 31, 2006
[Pseudoainhum and peripheral neuropathy]N Akallal, F Z Belgnaoui, H Benameur, 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.
Revue Du Rhumatisme (English Ed.)|July 27, 1999
Rigid spine syndrome. Two case-reportsR Niamane, N Birouk, A Benomar, 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.
Journal of the Neurological Sciences|March 4, 1999
Vitamin E deficiency ataxia associated with adenomaA Benomar, M Yahyaoui, N Marzouki, 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.
Revue Neurologique|January 1, 1994
[Dermatomyositis and Wilson disease]M el Alaoui-Faris, M Benabdeljalil, I Slassi, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Revue Neurologique|October 17, 1998
[Pure motor neuropathy after radiation therapy: 6 cases]T Lalu, B Mercier, N Birouk, et al.
Annales De Dermatologie Et De Venereologie|October 31, 2006
[Pseudoainhum and peripheral neuropathy]N Akallal, F Z Belgnaoui, H Benameur, 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.
Revue Du Rhumatisme (English Ed.)|July 27, 1999
Rigid spine syndrome. Two case-reportsR Niamane, N Birouk, A Benomar, 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.
Journal of the Neurological Sciences|March 4, 1999
Vitamin E deficiency ataxia associated with adenomaA Benomar, M Yahyaoui, N Marzouki, 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.
Revue Neurologique|January 1, 1994
[Dermatomyositis and Wilson disease]M el Alaoui-Faris, M Benabdeljalil, I Slassi, et al.
Pageof 4