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Results:
1-14
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Results: 14
Authors:
Kato, T
Hattori, H
Yorifuji, T
Tashiro, Y
Nakahata, T
Citation: T. Kato et al., Intracranial aneurysms in Ehlers-Danlos syndrome type IV in early childhood, PED NEUROL, 25(4), 2001, pp. 336-339
Authors:
Tanaka, K
Matsuno, E
Shimizu, E
Shibai, H
Yorifuji, T
Citation: K. Tanaka et al., Purification and characterization of aminopropionaldehyde dehydrogenase from Arthrobacter sp TMP-1, FEMS MICROB, 195(2), 2001, pp. 191-196
Authors:
Nagasaka, H
Yorifuji, T
Egawa, H
Kikuta, H
Tanaka, K
Kobayashi, K
Citation: H. Nagasaka et al., Successful living-donor liver transplantation from an asymptomatic carriermother in ornithine transcarbamylase deficiency, J PEDIAT, 138(3), 2001, pp. 432-434
Authors:
Ogata, T
Muroya, K
Matsuo, N
Shinohara, O
Yorifuji, T
Nishi, Y
Hasegawa, Y
Horikawa, R
Tachibana, K
Citation: T. Ogata et al., Turner syndrome and Xp deletions: Clinical and molecular studies in 47 patients, J CLIN END, 86(11), 2001, pp. 5498-5508
Authors:
Hattori, H
Yorifuji, T
Citation: H. Hattori et T. Yorifuji, Infantile convulsions and paroxysmal kinesigenic choreoathetosis in a patient with idiopathic hypoparathyroidism, BRAIN DEVEL, 22(7), 2000, pp. 449-450
Authors:
Siddiqui, JA
Shoeb, SM
Takayama, S
Shimizu, E
Yorifuji, T
Citation: Ja. Siddiqui et al., Purification and characterization of histamine dehydrogenase from Nocardioides simplex IFO 12069, FEMS MICROB, 189(2), 2000, pp. 183-187
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:
Nagasaka, H
Kobayashi, K
Yorifuji, T
Kage, M
Kimura, A
Takayanagi, M
Kikuta, H
Egawa, H
Tanaka, K
Inui, A
Fujisawa, T
Ohtake, A
Citation: H. Nagasaka et al., Indian childhood cirrhosis-like disease in a Japanese boy undergoing livertransplantation, J PED GASTR, 29(5), 1999, pp. 598-600
Authors:
Ueno, H
Katamura, K
Yorifuji, T
Ohmori, K
Kiyomasu, T
Iio, J
Ohmura, K
Mayumi, M
Citation: H. Ueno et al., Further characterization of memory T cells existing in a case of CD8 deficiency, HUMAN IMMUN, 60(11), 1999, pp. 1049-1053
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:
1-14
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