Current treatment for citrin deficiency during NICCD and adaptation/compensation stages: Strategy to prevent CTLN2 von Okano, Yoshiyuki, Ohura, Toshihiro, Sakamoto, Osamu, Inui, Ayano

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Analysis of daily energy, protein, fat, and carbohydrate intake in citrin-deficient patients: Towards prevention of adult-onset type II citrullinemia von Okano, Yoshiyuki, Okamoto, Miki, Yazaki, Masahide, Inui, Ayano, Ohura, Toshihiro, Murayama, Kei, Watanabe, Yoriko, Tokuhara, Daisuke, Takeshima, Yasuhiro

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Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan von Okano, Yoshiyuki, Kudo, Satoshi, Nishi, Yasuaki, Sakaguchi, Tomoko, Aso, Kazuyoshi

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Guide for diagnosis and treatment of hyperphenylalaninemia von Shintaku, Haruo, Ohura, Toshihiro, Takayanagi, Masaki, Kure, Shigeo, Owada, Misao, Matsubara, Yoichi, Yoshino, Makoto, Okano, Yoshiyuki, Ito, Tetsuya, Okuyama, Torayuki, Nakamura, Kimitoshi, Matuo, Masafumi, Endo, Fumio, Ida, Hiroyuki

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Reliability and validity of the PedsQL™ Multidimensional Fatigue Scale in Japan von Kobayashi, Kyoko, Okano, Yoshiyuki, Hohashi, Naohiro

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Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations von Chiu, Yen-Hui, Chang, Ying-Chen, Chang, Yu-Hsin, Niu, Dau-Ming, Yang, Yan-Ling, Ye, Jun, Jiang, Jianhui, Okano, Yoshiyuki, Lee, Dong Hwan, Pangkanon, Suthipong, Kuptanon, Chulaluck, Hock, Ngu Lock, Chiong, Mary Anne, Cavan, Barbra V, Hsiao, Kwang-Jen, Liu, Tze-Tze

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Wireless capsule endoscopy in pediatric patients: the first series from Japan von Tokuhara, Daisuke, Watanabe, Kenji, Okano, Yoshiyuki, Tada, Akio, Yamato, Kazumi, Mochizuki, Takahiro, Takaya, Junji, Yamano, Tsunekazu, Arakawa, Tetsuo

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Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening von Nagasaka, Hironori, Tsukahara, Hirokazu, Takatani, Tomozumi, Sanayama, Yoshitami, Takayanagi, Masaki, Ohura, Toshihiro, Sakamoto, Osamu, Ito, Tetsuya, Wada, Mika, Yoshino, Makoto, Ohtake, Akira, Yorifuji, Tohru, Hirayama, Satoshi, Miida, Takashi, Fujimoto, Hiroki, Mochizuki, Hiroshi, Hattori, Toshikazu, Okano, Yoshiyuki

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Fatigue and quality of life in citrin deficiency during adaptation and compensation stage von Okano, Yoshiyuki, Kobayashi, Kyoko, Ihara, Kenji, Ito, Tetsuya, Yoshino, Makoto, Watanabe, Yoriko, Kaji, Shunsaku, Ohura, Toshihiro, Nagao, Masayoshi, Noguchi, Atsuko, Mushiake, Sotaro, Hohashi, Naohiro, Hashimoto-Tamaoki, Tomoko

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Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination von Shimojima, Keiko, Okamoto, Nobuhiko, Suzuki, Yume, Saito, Mari, Mori, Masato, Yamagata, Tatanori, Momoi, Mariko Y, Hattori, Hideji, Okano, Yoshiyuki, Hisata, Ken, Okumura, Akihisa, Yamamoto, Toshiyuki

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Mechanism for increased hepatic glycerol synthesis in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse: Urine glycerol and glycerol 3-phosphate as... von Moriyama, Mitsuaki, Fujimoto, Yuki, Rikimaru, Shizuka, Ushikai, Miharu, Kuroda, Eishi, Kawabe, Kenji, Takano, Katsura, Asakawa, Akihiro, Inui, Akio, Eto, Kazuhiro, Kadowaki, Takashi, Sinasac, David S., Okano, Yoshiyuki, Yazaki, Masahide, Ikeda, Shu-ichi, Zhang, Chunhua, Song, Yuan-Zong, Sakamoto, Osamu, Kure, Shigeo, Mitsubuchi, Hiroshi, Endo, Fumio, Horiuchi, Masahisa, Nakamura, Yoichi, Yamamura, Ken-ichi, Saheki, Takeyori

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Nutritional status of patients with phenylketonuria in Japan von Okano, Yoshiyuki, Hattori, Toshikazu, Fujimoto, Hiroki, Noi, Kaori, Okamoto, Miki, Watanabe, Toshiaki, Watanabe, Ryoko, Fujii, Rika, Tamaoki, Tomoko

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Changes of lipoproteins in phenylalanine hydroxylase-deficient children during the first year of life von Nagasaka, Hironori, Tsukahara, Hirokazu, Okano, Yoshiyuki, Hirano, Ken-ichi, Sakurai, Toshihiro, Hui, Shu-Ping, Ohura, Toshihiro, Usui, Hiromi, Yorifuji, Tohru, Hirayama, Satoshi, Ohtake, Akira, Miida, Takashi

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Optimal serum phenylalanine for adult patients with phenylketonuria von Okano, Yoshiyuki, Nagasaka, Hironori

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Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency von Kimura, Akihiko, Kage, Masayoshi, Nagata, Ikuo, Mushiake, Sotaro, Ohura, Toshihiro, Tazawa, Yusaku, Maisawa, Shunichi, Tomomasa, Takeshi, Abukawa, Daiki, Okano, Yoshiyuki, Sumazaki, Ryo, Takayanagi, Masaki, Tamamori, Akiko, Yorifuji, Tohru, Yamato, Yasuhiko, Maeda, Kohji, Matsushita, Masami, Matsuishi, Toyojiro, Tanikawa, Ken, Kobayashi, Keiko, Saheki, Takeyori

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Intractable Absence Seizures in Hyperinsulinism-Hyperammonemia Syndrome von Nakano, Kousuke, MD, Kobayashi, Katsuhiro, MD, Okano, Yoshiyuki, MD, Aso, Kazuyoshi, MD, Ohtsuka, Yoko, MD

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Importance of molecular diagnosis in the accurate diagnosis of systemic carnitine deficiency von HITOMI, TOSHIAKI, MATSUURA, NORIO, SHIGEMATSU, YOSUKE, OKANO, YOSHIYUKI, SHINOZAKI, ERI, KAWAI, MASAHIKO, KOBAYASHI, HATASU, HARADA, KOUJI H., KOIZUMI, AKIO

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Evaluation of endogenous nitric oxide synthesis in congenital urea cycle enzyme defects von Nagasaka, Hironori, Tsukahara, Hirokazu, Yorifuji, Tohru, Miida, Takashi, Murayama, Kei, Tsuruoka, Tomoko, Takatani, Tomozumi, Kanazawa, Masaki, Kobayashi, Kunihiko, Okano, Yoshiyuki, Takayanagi, Masaki

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Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation von TAMAMORI, Akiko, OKANO, Yoshiyuki, OZAKI, Hajime, FUJIMOTO, Akie, KAJIWARA, Masue, FUKUDA, Kazuyoshi, KOBAYASHI, Keiko, SAHEKI, Takeyori, TAGAMI, Yasuko, YAMANO, Tsunekazu

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Protein‐losing gastropathy in a child and Guillain–Barré syndrome in a father caused by intrafamilial infection von Tokuhara, Daisuke, Hirokawa, Hidetetsu, Yamano, Tsunekazu, Okano, Yoshiyuki

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