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Journal of Inherited Metabolic Disease|May 11, 1999
Molecular heterogeneity of Krabbe diseaseL Fu, K Inui, T Nishigaki, et al.Journal of Neurology|December 1, 1990
A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studiesK Inui, R Namba, Y Ihara, et al.Brain & Development|June 1, 1997
Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2J Tanaka, T Nagai, H Arai, et al.Acta Neuropathologica|January 1, 1992
A case of pigmentary type of orthochromatic leukodystrophy with early onset and globoid cellsM Taniike, H Fujimura, S Kogaki, et al.Acta Paediatrica Scandinavica|September 1, 1979
Insulin and glucagon secretion in hepatic glycogenosesS Okada, Y Seino, H Kodama, et al.Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[The metabolism of radiolabelled GM1-ganglioside in cultured skin fibroblasts from controls and patients with GM1-gangliosidosis]K InuiNihon Rinsho. Japanese Journal of Clinical Medicine|February 1, 1993
[Molecular pathology of hepatic glycogen storage disease]K InuiThe Journal of Pediatrics|September 20, 2001
Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndromeI Yanagihara, K Inui, K Yanagihara, et al.Nihon Shishubyo Gakkai Kaishi|March 1, 1989
[Histological study of multinucleated giant cells in bone grafting]K Inui[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai|February 1, 1993
[Participation of platelet activating factor in the pulmonary injury during cardiopulmonary bypass]K InuiPageof 210