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Results: 1-6 |
Results: 6

Authors: Muroi, J Yorifuji, T Uematsu, A Shigematsu, Y Onigata, K Maruyama, H Nobutoki, T Kitamura, A Nakahata, T
Citation: J. Muroi et al., Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency, HUM GENET, 107(4), 2000, pp. 320-326

Authors: Muroi, J Yorifuji, T Uematsu, A Nakahata, T
Citation: J. Muroi et al., Cerebral infarction and pancreatitis: possible complications of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, J INH MET D, 23(6), 2000, pp. 636-637

Authors: Yorifuji, T Muroi, J Uematsu, A Nakahata, T Egawa, H Tanaka, K
Citation: T. Yorifuji et al., Living-related liver transplantation for neonatal-onset propionic acidemia, J PEDIAT, 137(4), 2000, pp. 572-574

Authors: Muroi, J Uematsu, A Yorifuji, T
Citation: J. Muroi et al., Identification of a novel single base-pair polymorphism in the glutamate dehydrogenase (GLUD1) gene, J HUM GENET, 44(4), 1999, pp. 268-269

Authors: Yorifuji, T Muroi, J Uematsu, A Hiramatsu, H Momoi, T
Citation: T. Yorifuji et al., Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics, HUM GENET, 104(6), 1999, pp. 476-479

Authors: Uematsu, A Yorifuji, T Muroi, J Yamanaka, C Momoi, T
Citation: A. Uematsu et al., Relatively longer hand in patients with Ullrich-Turner syndrome, AM J MED G, 82(3), 1999, pp. 254-256
Risultati: 1-6 |