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N Birouk

Showing results (1-10 of 36) with videos related to

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Revue Neurologique|December 3, 2014
[Review of the recent literature on hereditary neuropathies]N Birouk
La Revue De Medecine Interne|July 1, 2008
[Amyloid neuropathy resulting from an unknown protein]R Younsi, N Birouk, N Kissani
Stroke|April 1, 1994
Middle cerebral artery occlusion due to hydatid cysts of myocardial and intraventricular cavity cardiac origin. Two casesA Benomar, M Yahyaoui, N Birouk, et al.
Revue Neurologique|January 1, 1992
[Thrombosis of the upper longitudinal sinus and syphilitic cranial osteitis]M el Alaoui Faris, N Birouk, I Slassi, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1995
[Fahr syndrome and dysparathyroidism. 3 cases]A el Maghraoui, N Birouk, A Zaim, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Revue Neurologique|August 1, 1998
[Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification]N Birouk, T Maisonobe, N Le Forestier, et al.
Journal of Neurology|October 31, 2003
High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patientsA Bouhouche, A Benomar, N Birouk, et al.
Annals of Neurology|January 1, 1997
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A diseaseE LeGuern, R Gouider, D Mabin, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|November 29, 2005
[Autonomic profile of patients with migraine]H Benjelloun, N Birouk, I Slaoui, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Revue Neurologique|December 3, 2014
[Review of the recent literature on hereditary neuropathies]N Birouk
La Revue De Medecine Interne|July 1, 2008
[Amyloid neuropathy resulting from an unknown protein]R Younsi, N Birouk, N Kissani
Stroke|April 1, 1994
Middle cerebral artery occlusion due to hydatid cysts of myocardial and intraventricular cavity cardiac origin. Two casesA Benomar, M Yahyaoui, N Birouk, et al.
Revue Neurologique|January 1, 1992
[Thrombosis of the upper longitudinal sinus and syphilitic cranial osteitis]M el Alaoui Faris, N Birouk, I Slassi, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1995
[Fahr syndrome and dysparathyroidism. 3 cases]A el Maghraoui, N Birouk, A Zaim, et al.
Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.
Revue Neurologique|August 1, 1998
[Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification]N Birouk, T Maisonobe, N Le Forestier, et al.
Journal of Neurology|October 31, 2003
High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patientsA Bouhouche, A Benomar, N Birouk, et al.
Annals of Neurology|January 1, 1997
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A diseaseE LeGuern, R Gouider, D Mabin, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|November 29, 2005
[Autonomic profile of patients with migraine]H Benjelloun, N Birouk, I Slaoui, et al.
Pageof 4