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La Tunisie Medicale
|
March 1, 1976
[Myasthenia. Apropos of 13 cases]
B Hamida, S Samoud
La Tunisie Medicale
|
February 1, 1977
[Multiple sclerosis in Tunisia. Clinical study]
M Ben Hamida, S Samoud
La Nouvelle Presse Medicale
|
February 7, 1976
[Letter: Multiple sclerosis in Tunisia]
M Ben Hamida, S Samoud
La Tunisie Medicale
|
March 1, 1982
[Neurologic manifestations of Behçet's disease. Apropos of 27 cases]
M Ben Hamida, A Mrabet, S Samoud
La Nouvelle Presse Medicale
|
July 5, 1980
[Dacrystic epilepsy. A case]
M Ben Hamida, M Marzouki, C Duyckaerts, et al.
Journal of the Neurological Sciences
|
June 1, 1981
[Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases]
M Ben Hamida, F Letaief, C Ben Hamida, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 1, 1994
[Neurologic Behçet disease]
A Samoud, S Jebnoun, M Souid, et al.
La Tunisie Medicale
|
February 1, 1986
[Ulcero-mutilating acropathies and spinal abnormalities. Apropos of 4 case reports]
Z Sfar, S Lachaal, A Ben Saïd, et al.
L'Encephale
|
December 23, 2014
[Parvovirus B19 seroprevalence in a group of schizophrenic patients]
Y El Kissi, N Hannachi, A Mtiraoui, et al.
Journal De Genetique Humaine
|
August 1, 1986
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]
M Ben Hamida, H Chaabouni, S Madani, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
La Tunisie Medicale
|
March 1, 1976
[Myasthenia. Apropos of 13 cases]
B Hamida, S Samoud
La Tunisie Medicale
|
February 1, 1977
[Multiple sclerosis in Tunisia. Clinical study]
M Ben Hamida, S Samoud
La Nouvelle Presse Medicale
|
February 7, 1976
[Letter: Multiple sclerosis in Tunisia]
M Ben Hamida, S Samoud
La Tunisie Medicale
|
March 1, 1982
[Neurologic manifestations of Behçet's disease. Apropos of 27 cases]
M Ben Hamida, A Mrabet, S Samoud
La Nouvelle Presse Medicale
|
July 5, 1980
[Dacrystic epilepsy. A case]
M Ben Hamida, M Marzouki, C Duyckaerts, et al.
Journal of the Neurological Sciences
|
June 1, 1981
[Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases]
M Ben Hamida, F Letaief, C Ben Hamida, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 1, 1994
[Neurologic Behçet disease]
A Samoud, S Jebnoun, M Souid, et al.
La Tunisie Medicale
|
February 1, 1986
[Ulcero-mutilating acropathies and spinal abnormalities. Apropos of 4 case reports]
Z Sfar, S Lachaal, A Ben Saïd, et al.
L'Encephale
|
December 23, 2014
[Parvovirus B19 seroprevalence in a group of schizophrenic patients]
Y El Kissi, N Hannachi, A Mtiraoui, et al.
Journal De Genetique Humaine
|
August 1, 1986
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]
M Ben Hamida, H Chaabouni, S Madani, et al.
Page
of 2