Late-onset ornithine transcarbamylase deficiency in male patients: Prognostic factors and characteristics of plasma amino acid profile von HARADA, EIMEI, NISHIYORI, ATSUSHI, TOKUNAGA, YASUYUKI, WATANABE, YORIKO, KURIYA, NORIKAZU, KUMASHIRO, RYUKICHI, KUNO, TATEO, KUROMARU, RYUICHI, HIROSE, SHINICHI, ICHIKAWA, KOTARO, YOSHINO, MAKOTO

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Markers for Bone Metabolism in a Long-Lived Case of Thanatophoric Dysplasia von KUNO, TATEO, FUJITA, ICHIRO, MIYAZAKI, SUMIO, KATSUMATA, NORIYUKI

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Changes in Levels of Serum and Urinary Collagen-Related Substances in Growth Hormone Deficient Children Following Discontinuation of Growth Hormone Therapy von KUNO, TATEO, MIYAZAKI, SUMIO

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Normal Growth after Administration of Octreotide: Report on a Case of Persistent Hyperinsulinemic Hypoglycemia of Infancy Treated by Continuous Subcutaneous Injection of Octreotide von KUNO, TATEO, FUJITA, ICHIRO, OHTA, MITSUHIRO, KANEMITSU, HIRONOBU, MIYAZAKI, SUMIO, MIYAMOTO, SHICEKI

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The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients von NISHIYORI, A, YOSHINO, M, MORI, M, KATO, H, MATSUURA, T, HOSHIDE, R, MATSUDA, I, KUNO, T, MIYAZAKI, S, HIROSE, S.-I, KUROMARU, R.-I

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Continuous subcutaneous insulin injection for a case of mitochondrial cytopathy with diabetes mellitus requiring a large amount of insulin von Sato, TATEO KUNO, KATSUYA TASHIRO, TADASHI, Miyazaki, HAKARU TASAKI and SUMIO

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Continuous subcutaneous insulin injection for a case of mitochondrial cytopathy with diabetes mellitus requiring a large amount of insulin von Kuno, T, Tashiro, K, Sato, T, Tasaki, H, Miyazaki, S

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G370C Mutation in the FGFR3 Gene in a Japanese Patient with Thanatophoric Dysplasia von KATSUMATA, NORIYUKI, KUNO, TATEO, MIYAZAKI, SUMIO, MIKAMI, SHOKO, NAGASHIMA-MIYOKAWA, ATSUKO, NIMURA, ATSUKO, HORIKAWA, REIKO, TANAKA, TOSHIAKI

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A Huge Prolactinoma with Growth Retardation: Outcome of Three Years of Medical Treatment von Kuno, Tateo, Yamaguchi, Hideto, Miyazaki, Sumio

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Original Article: Late-onset ornithine transcarbamylase deficiency in male patients: Prognostic factors and characteristics of plasma amino acid profile von EIMEI HARADA, ATSUSHI NISHIYORI, YASUYUKI TOKUNAGA, YORIKO WATANABE, NORIKAZU KURIYA, RYUKICHI KUMASHIRO, TATEO KUNO, RYUICHI KUROMARU, SHINICHI HIROSE, Ichikawa, Kotaro, Yoshino, Makoto

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Biosynthesis and Degradation of γ-Glutamyltranspeptidase of Rat Kidney von MATSUDA, Yoshiko, TSUJI, Akihiko, KUNO, Tateo, KATUNUMA, Nobuhiko

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Exercise-induced acute renal failure in a girl with renai hypouricemia von SATO, TADASHI, KUNO, TATEO, TASHIRO, KATSUYA, FUJITA, ICHIRO, MIYAZAKI, SUMIO

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Rapid decrease of urinary pyridinoline excretion in growth hormone deficient children following discontinuation of growth hormone therapy von KUNO, TATEO, TASAKI, HAKARU, MIYAZAKI, SUMIO, HORIE, HITOSHI

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Clinical characteristics of Angelman syndrome patients with a non-IC-deleted imprinting mutation von Saitoh, Shinji, Wada, Takahito, Kuno, Tateo, Kim, Kyoung Chang, Ohashi, Hirofumi, Hashimoto, Katsuyo, Niikawa, Norio

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Late-onset type ornitine transcarbamirase deficiency (OTCD) with fulminant onset following a fatal prognosis von YASUTAKE, Tsutomu, NAGATOMO, Daisuke, MIZUTA, Toshihiko, EGUCHI, Yuichiro, KUMAGAI, Takanori, ARIO, Keisuke, OZAKI, Iwata, KUNO, Tateo, FUJIMOTO, Kazuma

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Preparation of Height and Weight Indices Calculator by using a Cellular Phone Platform von Tateo Kuno, Tsutomu Eguchi, Yuhei Hamasaki

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Increased serum level of IgG2 following splenectomy: case report von Koga, Hiroyuki, Kuno, Tateo, Miyazaki, Sumio

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Severely decompensated abdominal Wilson disease treated with peritoneal dialysis: A case report von KUNO, TATEO, HITOMI, TOMOHIRO, ZAITU, MASAFUMI, SATO, TADASHI, YOSHIDA, NOBUYUKI, MIYAZAKI, SUMIO

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A case of X-linked α-thalassemia/mental retardation syndrome: Analysis of hemoglobin by an automated glycated hemoglobin analyzer von KUNO, TATEO, IDEGUCHI, HIROSHI, YOSHIDA, NOBUYUKI, MASUYAMA, TATSUO, OHTA, MITSUHIRO, NISHIMURA, SHINJI, TASAKI, HAKARU, MIYAZAKI, SUMIO, HARA, HIROMICHI, MATSUMOTO, KAZUHIRO

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劇症型で発症し，不幸な転帰をとった遅発型オルニチントランスカルバミラーゼ欠損症の1例 von 安武, 努, 長友, 大輔, 水田, 敏彦, 江口, 有一郎, 熊谷, 貴文, 有尾, 啓介, 尾崎, 岩太, 久野, 建夫, 藤本, 一眞

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