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

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Acute-Onset Type 1 Diabetes that Developed During the Administration of Olanzapine von Iwaku, Kenji, Otuka, Fumiko, Taniyama, Matsuo

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Adult Thyroid Outcomes of Congenital Hypothyroidism von Sugisawa, Chiho, Narumi, Satoshi, Tanase-Nakao, Kanako, Ayako, Hoshiyama, Suzuki, Nami, Ohye, Hidemi, Fukushita, Miho, Matsumoto, Masako, Yoshihara, Ai, Watanabe, Natsuko, Sugino, Kiminori, Hishinuma, Akira, Noh, Jaeduk Yoshimura, Katoh, Ryohei, Taniyama, Matsuo, Ito, Koichi

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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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Multiple SNPs in intron 41 of thyroglobulin gene are associated with autoimmune thyroid disease in the Japanese population von Ban, Yoshiyuki, Tozaki, Teruaki, Taniyama, Matsuo, Skrabanek, Luce, Nakano, Yasuko, Ban, Yoshio, Hirano, Tsutomu

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Hepatotoxicity and cutaneous reactions after antithyroid drug administration von Otsuka, Fumiko, Noh, Jaeduk Y., Chino, Toshiko, Shimizu, Taeko, Mukasa, Koji, Ito, Kunihiko, Ito, Koichi, Taniyama, Matsuo

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NADPH Oxidase Deficiency Exacerbates Angiotensin II–Induced Abdominal Aortic Aneurysms in Mice von Kigawa, Yasuyoshi, Miyazaki, Takuro, Lei, Xiao-Feng, Nakamachi, Tomoya, Oguchi, Tatsunori, Kim-Kaneyama, Joo-ri, Taniyama, Matsuo, Tsunawaki, Shohko, Shioda, Seiji, Miyazaki, Akira

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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 von Sugisawa, Chiho, Higuchi, Shinji, Takagi, Masaki, Hasegawa, Yukihiro, Taniyama, Matsuo, Abe, Kiyomi, Hasegawa, Tomonobu, Narumi, Satoshi

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Genetic Variation in the Gene Encoding Adiponectin Is Associated With an Increased Risk of Type 2 Diabetes in the Japanese Population von HARA, Kazuo, BOUTIN, Philippe, KADOWAKI, Hiroko, HAGURA, Ryoko, AKANUMA, Yasuo, YAZAKI, Yoshio, NAGAI, Ryozo, TANIYAMA, Matsuo, MATSUBARA, Koichi, YODA, Madoka, NAKANO, Yasuko, KIMURA, Satoshi, MORI, Yasumichi, TOMITA, Motowo, ITO, Chikako, FROGUEL, Philippe, KADOWAKI, Takashi, TOBE, Kazuyuki, DINA, Christian, YASUDA, Kazuki, YAMAUCHI, Toshimasa, OTABE, Shuichi, OKADA, Terumasa, ETO, Kazuhiro

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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 von Sugisawa, Chiho, Abe, Kiyomi, Sunaga, Yuka, Taniyama, Matsuo, Hasegawa, Tomonobu, Narumi, Satoshi

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Metastatic Pancreatic Neuroendocrine Tumor that Progressed to Ectopic Adrenocorticotropic Hormone (ACTH) Syndrome with Growth Hormone-releasing Hormone (GHRH) Production von Tadokoro, Rie, Sato, Shotaro, Otsuka, Fumiko, Ueno, Makoto, Ohkawa, Shinichi, Katakami, Hideki, Taniyama, Matsuo, Nagasaka, Shoichiro

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Decrease in Serum Adiponectin Level Due to Obesity and Visceral Fat Accumulation in Children von Asayama, Kohtaro, Hayashibe, Hidemasa, Dobashi, Kazushige, Uchida, Norihiko, Nakane, Takaya, Kodera, Kohji, Shirahata, Akira, Taniyama, Matsuo

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Efficacy and Safety of the Dipeptidyl Peptidase-4 Inhibitor Sitagliptin on Atherosclerosis, β-Cell Function, and Glycemic Control in Japanese Patients with Type 2 Diabetes Mellitus... von Tsurutani, Yuya, MD, PhD, Omura, Masao, MD, PhD, Matsuzawa, Yoko, MD, PhD, Saito, Jun, MD, PhD, Higa, Mariko, MD, PhD, Taniyama, Matsuo, MD, PhD, Nishikawa, Tetsuo, MD, PhD

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A Case of Painless Thyroiditis in a Very Early Stage of Pregnancy von Sato, Shiori, Endo, Kei, Iizaka, Toru, Saiki, Ryo, Iwaku, Kenji, Sato, Shotaro, Takahashi, Yasuyoshi, Otsuka, Fumiko, Taniyama, Matsuo

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Occurrence of Type 1 Diabetes in Graves’ Disease Patients Who Are Positive for Antiglutamic Acid Decarboxylase Antibodies: An 8-Year Followup Study von Taniyama, Matsuo, Kasuga, Akira, Nagayama, Chieko, Ito, Koichi

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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 von Chiho Sugisawa, Shinji Higuchi, Masaki Takagi, Yukihiro Hasegawa, Matsuo Taniyama, Kiyomi Abe, Tomonobu Hasegawa, Satoshi Narumi

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PPAR[gamma ]2 gene Pro12Ala polymorphism may influence serum level of an adipocyte-derived protein, adiponectin, in the Japanese population von Yamamoto, Yukihiro, Hirose, Hiroshi, Miyashita, Kiichi, Nishikai, Kanako, Saito, Ikuo, Taniyama, Matsuo, Tomita, Motowo, Saruta, Takao

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Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia von Kawashiri, Masa-aki, Tada, Hayato, Hashimoto, Marowa, Taniyama, Matsuo, Nakano, Takamitsu, Nakajima, Katsuyuki, Inoue, Takeshi, Mori, Mika, Nakanishi, Chiaki, Konno, Tetsuo, Hayashi, Kenshi, Nohara, Atsushi, Inazu, Akihiro, Koizumi, Junji, Ishihara, Hirotaka, Kobayashi, Junji, Hirano, Tsutomu, Mabuchi, Hiroshi, Yamagishi, Masakazu

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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 von Chiho Sugisawa, Kiyomi Abe, Yuka Sunaga, Matsuo Taniyama, Tomonobu Hasegawa, Satoshi Narumi

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Vitamin D receptor initiation codon polymorphism influences genetic susceptibility to type 1 diabetes mellitus in the Japanese population von Ban, Y, Taniyama, M, Yanagawa, T, Yamada, S, Maruyama, T, Kasuga, A, Ban, Y

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