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R Gouider

Showing results (21-30 of 51) with videos related to

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La Tunisie Medicale|May 1, 2008
[Slow channel syndrome: clinical and neurophysiological aspects]I Ben Youssef Turki, I Kraoua, A Gargouri, et al.
Journal Francais D'Ophtalmologie|May 29, 2012
[Eye movement recordings in children with attention deficit hyperactivity disorder]A Gargouri-Berrechid, L Lanouar, I Kacem, et al.
Multiple Sclerosis and Related Disorders|December 20, 2021
Tunisian version of the brief international cognitive assessment for multiple sclerosis: Validation and normative valuesA Souissi, S Mrabet, W Ferchichi, et al.
Functional Neurology|June 8, 2000
Childhood diabetic neuropathy: a clinical and electrophysiological studyF el Bahri-Ben Mrad, R Gouider, M Fredj, 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.
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.
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.
Revue Neurologique|October 17, 1998
[Unverricht-Lündborg disease: clinical and electrophysiologic study of 19 Maghreb families]R Gouider, S Ibrahim, M Fredj, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
La Tunisie Medicale|May 1, 2008
[Slow channel syndrome: clinical and neurophysiological aspects]I Ben Youssef Turki, I Kraoua, A Gargouri, et al.
Journal Francais D'Ophtalmologie|May 29, 2012
[Eye movement recordings in children with attention deficit hyperactivity disorder]A Gargouri-Berrechid, L Lanouar, I Kacem, et al.
Multiple Sclerosis and Related Disorders|December 20, 2021
Tunisian version of the brief international cognitive assessment for multiple sclerosis: Validation and normative valuesA Souissi, S Mrabet, W Ferchichi, et al.
Functional Neurology|June 8, 2000
Childhood diabetic neuropathy: a clinical and electrophysiological studyF el Bahri-Ben Mrad, R Gouider, M Fredj, 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.
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.
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.
Revue Neurologique|October 17, 1998
[Unverricht-Lündborg disease: clinical and electrophysiologic study of 19 Maghreb families]R Gouider, S Ibrahim, M Fredj, et al.
Pageof 6