Diabetic family history in young Japanese persons with normal glucose tolerance associates with k-means clustering of glucose response to oral glucose load, insulinogenic index and... by Murai, Norimitsu, Saito, Naoko, Nii, Sayuri, Nishikawa, Yuto, Suzuki, Asami, Kodama, Eriko, Iida, Tatsuya, Mikura, Kentaro, Imai, Hideyuki, Hashizume, Mai, Kigawa, Yasuyoshi, Tadokoro, Rie, Sugisawa, Chiho, Endo, Kei, Iizaka, Toru, Otsuka, Fumiko, Ishibashi, Shun, Nagasaka, Shoichiro

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Insulin and Proinsulin Dynamics Progressively Deteriorate From Within the Normal Range Toward Impaired Glucose Tolerance by Murai, Norimitsu, Saito, Naoko, Kodama, Eriko, Iida, Tatsuya, Mikura, Kentaro, Imai, Hideyuki, Kaji, Mariko, Hashizume, Mai, Kigawa, Yasuyoshi, Koizumi, Go, Tadokoro, Rie, Sugisawa, Chiho, Endo, Kei, Iizaka, Toru, Saiki, Ryo, Otsuka, Fumiko, Ishibashi, Shun, Nagasaka, Shoichiro

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Inactivation of a Frameshift TSH Receptor Variant Val711 Phefs 18 is Due to Acquisition of a Hydrophobic Degron by Sugisawa, Chiho, Ono, Makoto, Kashimada, Kenichi, Hasegawa, Tomonobu, Narumi, Satoshi

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Therapeutic efficacy and limitations of potassium iodide for patients newly diagnosed with Graves' disease by Nami Suzuki, Jaeduk Yoshimura Noh, Chiho Sugisawa, Ayako Hoshiyama, Marino Hiruma, Akiko Kawaguchi, Mitsuha Morisaki, Hidemi Ohye, Miho Suzuki, Masako Matsumoto, Yo Kunii, Ai Yoshihara, Natsuko Watanabe, Kiminori Sugino, Kochi Ito

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Mild thyroid peroxidase deficiency caused by TPO mutations with residual activity : Correlation between clinical phenotypes and enzymatic activity by Satoshi Narumi, Larry A Fox, Keisuke Fukudome, Zenichi Sakaguchi, Chiho Sugisawa, Kiyomi Abe, Kaori Kameyama, Tomonobu Hasegawa

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Homozygous DUOXA2 mutation (p.Tyr138) in a girl with congenital hypothyroidism and her apparently unaffected brother : Case report and review of the literature by Chiho Sugisawa, Shinji Higuchi, Masaki Takagi, Yukihiro Hasegawa, Matsuo Taniyama, Kiyomi Abe, Tomonobu Hasegawa, Satoshi Narumi

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Aldosterone excess may inhibit insulin secretion : A comparative study on glucose metabolism pre- and post-adrenalectomy in patients with primary aldosteronism by Yuya Tsurutani, Chiho Sugisawa, Akiko Ishida, Kosuke Inoue, Jun Saito, Masao Omura, Shoichiro Nagasaka, Tetsuo Nishikawa

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Identification of compound heterozygous TSHR mutations (R109Q and R450H) in a patient with nonclassic TSH resistance and functional characterization of the mutant receptors by Chiho Sugisawa, Kiyomi Abe, Yuka Sunaga, Matsuo Taniyama, Tomonobu Hasegawa, Satoshi Narumi

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Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review by Sugisawa, Chiho, Taniyama, Matsuo, Sato, Takeshi, Takahashi, Yasuyoshi, Hasegawa, Tomonobu, Narumi, Satoshi

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Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects by Tanase-Nakao, Kanako, Iwahashi-Odano, Megumi, Sugisawa, Chiho, Abe, Kiyomi, Muroya, Koji, Yamamoto, Yukiyo, Kawada, Yasusada, Mushimoto, Yuichi, Ohkubo, Kazuhiro, Kinjo, Saori, Shimura, Kazuhiro, Aoyama, Kohei, Mizuno, Haruo, Hotsubo, Tomoyuki, Takahashi, Chie, Isojima, Tsuyoshi, Kina, Yoko, Takakuwa, Satoshi, Hamada, Junpei, Sawaki, Miwa, Shigehara, Keiichi, Sugimoto, Satoru, Etani, Yuri, Narumi-Wakayama, Hiroko, Mine, Yusuke, Hasegawa, Tomonobu, Hishinuma, Akira, Narumi, Satoshi

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Clinical characteristics and efficacy of pioglitazone in a Japanese patient with familial partial lipodystrophy due to peroxisome proliferator-activated receptor γ gene mutation by Iizaka, Toru, Kodama, Eriko, Mikura, Kentaro, Iida, Tatsuya, Imai, Hideyuki, Hashizume, Mai, Kigawa, Yasuyoshi, Sugisawa, Chiho, Tadokoro, Rie, Endo, Kei, Otsuka, Fumiko, Isoda, Masayo, Ebihara, Ken, Ishibashi, Shun, Nagasaka, Shoichiro

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Secondary Hypogonadism due to Excessive Ingestion of Isoflavone in a Man by Imai, Hideyuki, Nishikawa, Hiroto, Suzuki, Asami, Kodama, Eriko, Iida, Tatsuya, Mikura, Kentaro, Hashizume, Mai, Kigawa, Yasuyoshi, Tadokoro, Rie, Sugisawa, Chiho, Endo, Kei, Iizaka, Toru, Otsuka, Fumiko, Nagasaka, Shoichiro

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Association of ghrelin dynamics with beta cell function in Japanese subjects with normal glucose tolerance by Murai, Norimitsu, Saito, Naoko, Kodama, Eriko, Iida, Tatsuya, Mikura, Kentaro, Imai, Hideyuki, Kaji, Mariko, Hashizume, Mai, Kigawa, Yasuyoshi, Koizumi, Go, Tadokoro, Rie, Sugisawa, Chiho, Endo, Kei, Iizaka, Toru, Saiki, Ryo, Otsuka, Fumiko, Shun, Ishibashi, Nagasaka, Shoichiro

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Therapeutic efficacy and limitations of potassium iodide for patients newly diagnosed with Graves’ disease by Suzuki, Nami, Noh, Jaeduk Yoshimura, Sugisawa, Chiho, Hoshiyama, Ayako, Hiruma, Marino, Kawaguchi, Akiko, Morisaki, Mitsuha, Ohye, Hidemi, Suzuki, Miho, Matsumoto, Masako, Kunii, Yo, Yoshihara, Ai, Watanabe, Natsuko, Sugino, Kiminori, Ito, Kochi

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Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects by Tanase-Nakao, Kanako, Iwahashi-Odano, Megumi, Sugisawa, Chiho, Abe, Kiyomi, Muroya, Koji, Yamamoto, Yukiyo, Kawada, Yasusada, Mushimoto, Yuichi, Ohkubo, Kazuhiro, Kinjo, Saori, Shimura, Kazuhiro, Aoyama, Kohei, Mizuno, Haruo, Hotsubo, Tomoyuki, Takahashi, Chie, Isojima, Tsuyoshi, Kina, Yoko, Takakuwa, Satoshi, Hamada, Junpei, Sawaki, Miwa, Shigehara, Keiichi, Sugimoto, Satoru, Etani, Yuri, Narumi-Wakayama, Hiroko, Mine, Yusuke, Hasegawa, Tomonobu, Hishinuma, Akira, Narumi, Satoshi

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Clinical characteristics and efficacy of pioglitazone in a Japanese patient with familial partial lipodystrophy due to peroxisome proliferator-activated receptor γ gene mutation by Toru Iizaka, Eriko Kodama, Kentaro Mikura, Tatsuya Iida, Hideyuki Imai, Mai Hashizume, Yasuyoshi Kigawa, Chiho Sugisawa, Rie Tadokoro, Kei Endo, Fumiko Otsuka, Masayo Isoda, Ken Ebihara, Shun Ishibashi, Shoichiro Nagasaka

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A case of 3 months old Japanese boy with sporadic congenital none-autoimmune hyperthyroidism by Kinjo, Saori, Kanno, Masayuki, Matayoshi, Kei, Takefuta, Kiyotaka, Izumi, Ayako, Sugisawa, Chiho, Narumi, Satoshi, Kohama, Moriyasu

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