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Revue Neurologique|February 1, 1977
[Multiple sclerosis in Tunisia. Clinical study of 100 cases]M B HamidaJournal of the Neurological Sciences|March 1, 1980
[Structural and ultrastructural quantitative study of skin and nerve biopsies in the diagnosis of congenital indifference to pain]C B Hamida, F SamoudaAnnales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|October 1, 1977
[Multiple sclerosis in Tunisia: cochleo-vestibular study (author's transl)]A Belkahia, M B Hamida, H BouzouitaNeurology|April 6, 2000
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian familyN Mrissa, S Belal, C B Hamida, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1974
[Valvular prosthesis and anticoagulant treatment]M B Ismail, B Hamida, M T Maamouri, et al.Neurology|April 13, 2000
Clinical and genetic study of familial Parkinson's disease in TunisiaN Gouider-Khouja, S Belal, M B Hamida, et al.Orthopaedics & Traumatology, Surgery & Research : OTSR|March 5, 2011
Endoscopically assisted reconstruction of acute acromioclavicular joint dislocation using a synthetic ligament. Outcomes at 12 monthsG Cohen, P Boyer, N Pujol, et al.General Physiology and Biophysics|August 14, 2013
Protective effects of Artemisia campestris upon fenthion-induced nephrotoxicity in adult rats and their progenyMediha Sefi, Afef Troudi, Fatma B Hamida, 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.Pageof 3