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Muscle & Nerve|May 8, 1998
Mitochondrial abnormalities in selenium-deficient myopathyY Osaki, I Nishino, N Murakami, et al.Biochemical and Biophysical Research Communications|April 16, 1998
Glycogen storage disease type II: identification of four novel missense mutations (D645N, G648S, R672W, R672Q) and two insertions/deletions in the acid alpha-glucosidase locus of patients of differing phenotypeM L Huie, S Tsujino, S Sklower Brooks, et al.Clinical Genetics|January 19, 2018
NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathyA Ishiyama, K Muramatsu, S Uchino, et al.Neurology|April 1, 1996
Interferon-alpha is effective in HTLV-I-associated myelopathy: a multicenter, randomized, double-blind, controlled trialS Izumo, I Goto, Y Itoyama, et al.Clinical Genetics|February 27, 2016
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?A Fujita, C Waga, Y Hachiya, et al.No to Shinkei = Brain and Nerve|April 13, 1999
[The clinical usefulness of high-dose intravenous immunoglobulin therapy for chronic inflammatory demyelinating polyneuropathy and multifocal motor neuropathy]T Kubori, T Mezaki, R Kaji, et al.Pageof 28