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Diabetes Care|June 1, 1993
Hypersensitivity to insulin during remissions in cyclosporin-treated IDDM patientsR G Burcelin, M Eddouks, M Beylot, et al.Clinical and Experimental Rheumatology|January 1, 1991
Latent hepatitis B virus (HBV) infection in systemic necrotizing vasculitisP Marcellin, Y Calmus, H Takahashi, et al.Proceedings of the National Academy of Sciences of the United States of America|June 1, 1989
A monoclonal anti-double-stranded DNA autoantibody binds to a 94-kDa cell-surface protein on various cell types via nucleosomes or a DNA-histone complexL Jacob, J P Viard, B Allenet, et al.Allergy|July 22, 2014
Casein-specific IL-4- and IL-13-secreting T cells: a tool to implement diagnosis of cow's milk allergyB Michaud, J Aroulandom, N Baiz, et al.Revue Neurologique|January 1, 1994
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]A Joutel, M G Bousser, V Biousse, et al.Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.Human Genetics|November 1, 1996
Age-dependent penetrance and mapping of the locus for juvenile and early-onset open-angle glaucoma on chromosome 1q (GLC1A) in a French familyA Meyer, A Béchetoille, F Valtot, et al.Nature Genetics|September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19A Joutel, M G Bousser, V Biousse, et al.Journal of Medical Genetics|July 1, 1997
Genetic heterogeneity of primary open angle glaucoma and ocular hypertension: linkage to GLC1A associated with an increased risk of severe glaucomatous optic neuropathyA P Brézin, A Béchetoille, P Hamard, et al.Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.Pageof 57