Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review von Sugisawa, Chiho, Takamizawa, Tetsuya, Abe, Kiyomi, Hasegawa, Tomonobu, Shiga, Kentaro, Sugawara, Hidenori, Ohsugi, Koji, Muroya, Koji, Asakura, Yumi, Adachi, Masanori, Daitsu, Takashi, Numakura, Chikahiko, Koike, Akemi, Tsubaki, Junko, Kitsuda, Kazuteru, Matsuura, Nobuo, Taniyama, Matsuo, Ishii, Sumiyasu, Satoh, Tetsurou, Yamada, Masanobu, Narumi, Satoshi

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Relapse of Salmonella Saintpaul meningitis in a 4‐month‐old infant von Daitsu, Takashi, Maeda, Shoko, Abe, Akiko, Kanazawa, Chikako, Shimizu, Yukitoshi

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A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus von Daitsu, Takashi, Igaki, Junko, Goto, Masahiro, Hasegawa, Yukihiro

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A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus von Takashi Daitsu, Junko Igaki, Masahiro Goto, Yukihiro Hasegawa

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Two patients with HNF4A -related congenital hyperinsulinism and renal tubular dysfunction: A clinical variation which includes transient hepatic dysfunction von Numakura, Chikahiko, Hashimoto, Yukiko, Daitsu, Takashi, Hayasaka, Kiyoshi, Mitsui, Tetsuo, Yorifuji, Tohru

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