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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.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.Annales Francaises D'Anesthesie Et De Reanimation|July 25, 2006
[Thrombotic microangiopathies in the intensive care unit]M Bahloul, C Ben Hamida, H Dammak, 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.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 19q13.3A 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 mutationM 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 syndromeN Soussi-Yanicostas, C Ben Hamida, G S Butler-Browne, et al.Acta Neuropathologica|June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patientA Larnaout, S Belal, M Zouari, et al.Neuromuscular Disorders : NMD|August 26, 1998
Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiencyM Zouari, M Feki, C Ben Hamida, et al.Journal Des Maladies Vasculaires|May 11, 2007
[Thrombotic microangiopathies. Incidence, pathogenesis, diagnosis, treatment and prognosis]M Bahloul, H Dammak, H Kallel, et al.Pageof 6