Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report von Yamada, Kenji, Ito, Michinori, Kobayashi, Hironori, Hasegawa, Yuki, Fukuda, Seiji, Yamaguchi, Seiji, Taketani, Takeshi

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Ghrelin Concentration in Cord and Neonatal Blood: Relation to Fetal Growth and Energy Balance von Kitamura, Seiko, Yokota, Ichiro, Hosoda, Hiroshi, Kotani, Yumiko, Matsuda, Junko, Naito, Etsuo, Ito, Michinori, Kangawa, Kenji, Kuroda, Yasuhiro

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Presumed hypoplastic intrahepatic portal system due to patent ductus venosus: Importance of direct occlusion test of ductus venosus under open laparotomy von Takehara, Yuka, Mori, Kazuhiro, Edagawa, Takuji, Sugimoto, Mayumi, Takehara, Hiroo, Ito, Michinori, Kuroda, Yasuhiro

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Dynamic changes in serum leptin concentrations during the fetal and neonatal periods von MATSUDA, J, YOKOTA, I, IIDA, M, MURAKAMI, T, YAMADA, M, SAIJO, T, NAITO, E, ITO, M, SHIMA, K, KURODA, Y

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Serum Leptin Concentration in Cord Blood: Relationship to Birth Weight and Gender von Matsuda, Junko, Yokota, Ichiro, Iida, Mitsuru, Murakami, Takashi, Naito, Etsuo, Ito, Michinori, Shima, Kenji, Kuroda, Yashuhiro

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Effects of long-term zinc treatment in Japanese patients with Wilson disease: efficacy, stability, and copper metabolism von Shimizu, Norikazu, Fujiwara, Junko, Ohnishi, Shin, Sato, Mari, Kodama, Hiroko, Kohsaka, Takao, Inui, Ayano, Fujisawa, Tomoo, Tamai, Hiroshi, Ida, Shinobu, Itoh, Susumu, Ito, Michinori, Horiike, Norio, Harada, Masaru, Yoshino, Makoto, Aoki, Tsugutoshi

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Adrenocorticotropic hormone therapy for infantile spasms alters pyruvate metabolism in the central nervous system von Miyazaki, Masahito, Hashimoto, Toshiaki, Yoneda, Yoshihiro, Saijio, Takahiko, Mori, Kenji, Ito, Michinori, Kuroda, Yasuhiro

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Mutations in the X-linked pyruvate dehydrogenase (E1) α subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency von Lissens, Willy, De Meirleir, Linda, Seneca, Sara, Liebaers, Inge, Brown, Garry K., Brown, Ruth M., Ito, Michinori, Naito, Etsuo, Kuroda, Yasuhiro, Kerr, Douglas S., Wexler, Isaiah D., Patel, Mulchand S., Robinson, Brian H., Seyda, Agnieszka

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Management of acute metabolic decompensation in maple syrup urine disease: A multi-center study von Yoshino, Makoto, Aoki, Kikumaro, Akeda, Hideki, Hashimoto, Kazuko, Ikeda, Tetsuo, Inoue, Fumio, Ito, Michinori, Kawamura, Masahiko, Kohno, Yoshinori, Koga, Yasutoshi, Kuroda, Yasuhiro, Maesaka, Hatae, Murakami-Soda, Hiroko, Sugiyama, Naruji, Suzuki, Yasuyuki, Yoshioka, Shoji Yano1 And Akira

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Molecular genetic analysis of pyridoxine-nonresponsive homocystinuric siblings with different blood methionine levels during the neonatal period von Chen, S, Ito, M, Saijo, T, Naito, E, Kuroda, Y

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Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region von Naito, Etsuo, Ito, Michinori, Yokota, Ichiro, Saijo, Takahiko, Matsuda, Junko, Ogawa, Yukiko, Kitamura, Seiko, Takada, Eiko, Horii, Yoshihiro, Kuroda, Yasuhiro

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Association between vitamin D receptor genotype and age of onset in juvenile Japanese patients with type 1 diabetes von Yokota, Ichiro, Satomura, Shigeko, Kitamura, Seiko, Taki, Yumiko, Naito, Etsuo, Ito, Michinori, Nisisho, Kahoru, Kuroda, Yasuhiro

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Fluorescence in situ Hybridization Useful in Clinical Analysis to Search Quickly for Deletion of the Chromosome 22 for Diagnosis of Atypical Teratoid/rhabdoid Tumor von SONE, Michiko, IWAI, Tsuyako, POOH, Kyonhon, NAKAJIMA, Kouhei, HIRABE, Saburo, YOKOTA, Ichiro, ITO, Michinori, NAKAGAWA, Yoshinobu

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Two siblings with vitamin B6-nonresponsive cystathionine beta-synthase deficiency and differing blood methionine levels during the neonatal period von Watanabe, T, Ito, M, Naito, E, Yokota, I, Matsuda, J, Kuroda, Y

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Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency von Naito, Etsuo, Ito, Michinori, Yokota, Ichiro, Saijo, Takahiko, Ogawa, Yukiko, Kuroda, Yasuhiro

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Sisters with α-mannosidosis and systemic lupus erythematosus von URUSHIHARA, Maki, KAGAMI, Shoji, YASUTOMO, Koji, ITO, Michinori, KONDO, Shuji, KITAMURA, Akiko, MALM, Dag, KLENOW, Helle, NILSSEN, Oivind, KURODA, Yasuhiro

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Collection and Transplantation of Peripheral Blood Stem Cells in Very Small Children Weighing 20 kg or Less von Takaue, Yoichi, Kawano, Yoshifumi, Abe, Takanori, Okamoto, Yasuhiro, Suzue, Takeshi, Shimizu, Takashi, Saito, Shinichi, Sato, Junko, Makimoto, Atsushi, Nakagawa, Ryuji, Watanabe, Tsutomu, Ito, Michinori, Kuroda, Yasuhiro

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Authors’ Response: N-Octanoylated Ghrelin Levels in Cord and Neonatal Blood von Kitamura, Seiko, Yokota, Ichiro, Hosoda, Hiroshi, Kotani, Yumiko, Matsuda, Junko, Naito, Etsuo, Ito, Michinori, Kangawa, Kenji, Kuroda, Yasuhiro

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N-Octanoylated Ghrelin Levels in Cord and Neonatal Blood von Ferrero, Simone

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UNDERWATER LINE FOR USE IN SWEETFISH DECOY-FISHING DEVICE AND SWEETFISH FISHING METHOD BY SWEETFISH DECOY-FISHING DEVICE USING THE SAME von ITO MICHINORI

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