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Genes, Chromosomes & Cancer|October 1, 1995
Chromosomes in gliomatosis cerebriB K Hecht, C Turc-Carel, M Chatel, et al.Human Immunology|March 1, 1995
TAP2 gene polymorphism contributes to genetic susceptibility to multiple sclerosisH Moins-Teisserenc, G Semana, M Alizadeh, et al.Revue Neurologique|February 19, 2022
Ten-year follow-up after mitoxantrone induction for early highly active relapsing-remitting multiple sclerosis: An observational study of 100 consecutive patientsM Lefort, G Le Corre, E Le Page, et al.La Nouvelle Presse Medicale|February 3, 1979
[Demonstration by iron overloading study and HLA genotyping of recessive transmission of idiopathic haemochromatosis in two pseudodominant pedigrees (author's transl)]M Simon, J P Hespel, R Fauchet, et al.Journal of Neuroimmunology|February 2, 2010
MGAT5 alters the severity of multiple sclerosisB Brynedal, J Wojcik, F Esposito, et al.Pediatrie|January 1, 1993
[Congenital intrahepatic arterio-portal fistula: diagnostic and therapeutic aspects]C Meunier, A Dabadie, P Darnault, et al.The EMBO Journal|May 1, 1991
Primary structure of a collagenic tail peptide of Torpedo acetylcholinesterase: co-expression with catalytic subunit induces the production of collagen-tailed forms in transfected cellsE Krejci, F Coussen, N Duval, et al.Neurology|September 26, 2002
Cardiac adverse effects associated with mitoxantrone (Novantrone) therapy in patients with MSR G Ghalie, G Edan, M Laurent, et al.Neurology|March 24, 2004
Acute aphasia in multiple sclerosis: A multicenter study of 22 patientsA Lacour, J De Seze, E Revenco, et al.Presse Medicale (Paris, France : 1983)|November 5, 1997
[Cerebral vascular complication of hyperhomocysteinemia. Controlling thromboembolic complications with folates]M Candito, P Bedoucha, D Jambou, et al.Pageof 25