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F Hentati

Showing results (51-60 of 120) with videos related to

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La Tunisie Medicale|June 1, 1990
[Pompe's disease: a report of 3 cases (clinical, biochemical, anatomo-pathological study]M F Ben Dridi, A Samoud, N Tebib, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young childrenS Decary, C B Hamida, V Mouly, et al.
Neuromuscular Disorders : NMD|June 19, 1998
LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3C G Bönnemann, J Wong, C Ben Hamida, et al.
Revue Neurologique|March 31, 2005
[Behçet's disease associated with peripheral neuropathy]I Ben Ghorbel, Z Ibnelhadj, M Zouari, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 21, 2009
Man-in-the-barrel syndrome with combination of infarctions in the anterior spinal artery and posterior inferior cerebellar artery territoriesS Ben Sassi, G El Euch, A Regaieg, et al.
Muscle & Nerve|April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophyC 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 diseaseK Hamzaoui, A Hamzaoui, F Hentati, et al.
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 diseaseN Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Pageof 12

Showing results (51-60 of 120) with videos related to

Sort By:
Pageof 12
La Tunisie Medicale|June 1, 1990
[Pompe's disease: a report of 3 cases (clinical, biochemical, anatomo-pathological study]M F Ben Dridi, A Samoud, N Tebib, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young childrenS Decary, C B Hamida, V Mouly, et al.
Neuromuscular Disorders : NMD|June 19, 1998
LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3C G Bönnemann, J Wong, C Ben Hamida, et al.
Revue Neurologique|March 31, 2005
[Behçet's disease associated with peripheral neuropathy]I Ben Ghorbel, Z Ibnelhadj, M Zouari, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 21, 2009
Man-in-the-barrel syndrome with combination of infarctions in the anterior spinal artery and posterior inferior cerebellar artery territoriesS Ben Sassi, G El Euch, A Regaieg, et al.
Muscle & Nerve|April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophyC 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 diseaseK Hamzaoui, A Hamzaoui, F Hentati, et al.
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 diseaseN Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Pageof 12