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Medical and Pediatric Oncology|January 1, 1980
Hypoglycemia in a child with hepatoblastomaK Ha, T Ikeda, S Okada, et al.Brain & Development|November 1, 1993
Evaluation of myelination by means of the T2 value on magnetic resonance imagingJ Ono, R Kodaka, K Imai, et al.Enzyme|January 1, 1987
Biochemical heterogeneity in I-cell disease. Sucrose-loading test classifies two distinct subtypesS Okada, K Inui, M Furukawa, et al.Journal of Human Genetics|March 4, 2000
Mutation analysis of two Japanese patients with Fanconi-Bickel syndromeM Akagi, K Inui, S Nakajima, et al.Journal of the Neurological Sciences|August 1, 1995
Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural studyM Kaido, H Fujimura, M Taniike, et al.Biochemistry International|August 1, 1988
Biochemical studies on lymphoblastoid cells with inherited N-acetyl-glucosamine 1-phosphotransferase deficiency (I-cell disease)S Okada, M Handa, T Hashimoto, et al.Qualitative Health Research|May 2, 2000
Aboriginal grandmothers' experience with health promotion and participatory action researchG DicksonRinsho Byori. the Japanese Journal of Clinical Pathology|August 25, 2001
[Therapeutic drug monitoring of immunosuppresants]T Hashida, K InuiJournal of Neurophysiology|December 1, 1993
Target site of inhibition mediated by midbrain periaqueductal gray matter of baroreflex vagal bradycardiaK Inui, S NosakaNihon Rinsho. Japanese Journal of Clinical Medicine|May 1, 1996
[Thoracoscopic surgery]K Inui, S HitomiPageof 210