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La Tunisie Medicale
|
June 1, 1986
[Case of the rigid spine syndrome in a female patient]
M Ben Hamida, F Hentati, C Ben Hamida, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Evolution of muscle specific proteins in Werdnig-Hoffman's disease
N Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
C B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Muscle & Nerve
|
April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy
C Ben Hamida, N Soussi-Yanicostas, G S Butler-Browne, et al.
The Journal of Rheumatology
|
December 1, 1994
Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease
K Hamzaoui, A Hamzaoui, F Hentati, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
A Driss, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
M Kefi, R Amouri, A Driss, et al.
Journal of the Neurological Sciences
|
July 1, 1991
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome
N Soussi-Yanicostas, C Ben Hamida, G S Butler-Browne, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study
A Larnaout, M A Mongalgi, N Kaabachi, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
May 26, 2017
Congenital anomalies in Tunisia: Frequency and risk factors
M Aloui, K Nasri, N Ben Jemaa, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 112) with videos related to
Sort By:
Page
of 12
La Tunisie Medicale
|
June 1, 1986
[Case of the rigid spine syndrome in a female patient]
M Ben Hamida, F Hentati, C Ben Hamida, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Evolution of muscle specific proteins in Werdnig-Hoffman's disease
N Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
C B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Muscle & Nerve
|
April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy
C Ben Hamida, N Soussi-Yanicostas, G S Butler-Browne, et al.
The Journal of Rheumatology
|
December 1, 1994
Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease
K Hamzaoui, A Hamzaoui, F Hentati, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
A Driss, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
M Kefi, R Amouri, A Driss, et al.
Journal of the Neurological Sciences
|
July 1, 1991
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome
N Soussi-Yanicostas, C Ben Hamida, G S Butler-Browne, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study
A Larnaout, M A Mongalgi, N Kaabachi, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
May 26, 2017
Congenital anomalies in Tunisia: Frequency and risk factors
M Aloui, K Nasri, N Ben Jemaa, et al.
Page
of 12