Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan von Shibata, Nao, Numakura, Chikahiko, Hamajima, Takashi, Miyako, Kenichi, Fujiwara, Ikuma, Mori, Jun, Saitoh, Akihiko, Nagasaki, Keisuke

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A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy von Furuzono, Miwa, Makimura, Mika, Miyako, Kenichi

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Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version von Urakami, Tatsuhiko, Hotsubo, Tomoyuki, Ogawa, Yohei, Kikuchi, Toru, Usuda, Rika, Matsui, Katsuyuki, Hirose, Masakazu, Hirai, Hiroki, Abiru, Norio, Fujiwara, Ikuma, Mizuno, Haruo, Miyako, Kenichi, Takahashi, Kazuma, Shimada, Akira

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Clinical and Genetic Characteristics in Patients With Gitelman Syndrome von Fujimura, Junya, Nozu, Kandai, Yamamura, Tomohiko, Minamikawa, Shogo, Nakanishi, Keita, Horinouchi, Tomoko, Nagano, China, Sakakibara, Nana, Nakanishi, Koichi, Shima, Yuko, Miyako, Kenichi, Nozu, Yoshimi, Morisada, Naoya, Nagase, Hiroaki, Ninchoji, Takeshi, Kaito, Hiroshi, Iijima, Kazumoto

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Age-Related Clinical Characteristics of Isolated Congenital Unilateral Absence of a Pulmonary Artery von Koga, Hiroshi, Hidaka, Tomoko, Miyako, Kenichi, Suga, Naohiro, Takahashi, Noboru

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Two Cases of New-onset Pediatric Diabetes With Delayed Diagnosis and Treatment Due to the Coronavirus Disease 2019 Pandemic von Makimura, Mika, Furuzono, Miwa, Miyako, Kenichi

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A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency von Kawano, Atsuko, Kohno, Hitoshi, Miyako, Kenichi

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Improving circulatory disturbance in transient abnormal myelopoiesis von Koga, Hiroshi, Miyako, Kenichi, Suga, Naohiro, Hidaka, Tomoko, Takahashi, Noboru

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PAPA-1 Is a Nuclear Binding Partner of IGFBP-2 and Modulates Its Growth-Promoting Actions von Miyako, Kenichi, Cobb, Laura J, Francis, Malik, Huang, Alden, Peng, Bonnie, Pintar, John E, Ariga, Hiroyoshi, Cohen, Pinchas

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Predisposition to Subdural Hemorrhage in X-Linked Myotubular Myopathy von Koga, Hiroshi, MD, Miyako, Kenichi, MD, PhD, Suga, Naohiro, MD, PhD, Hidaka, Tomoko, MD, Takahashi, Noboru, MD, PhD

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Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus von Miyako, Kenichi, Yamaguchi, Yui, Sakemi, Yoshihiro, Suga, Naohiro, Utsunomiya, Rina, Takahashi, Noboru

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Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome von Tanaka, Wataru, Oyama, Noriko, Makimura, Mika, Miyako, Kenichi

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Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited von Ishii, Tomohiro, Tajima, Toshihiro, Kashimada, Kenichi, Mukai, Tokuo, Tanahashi, Yusuke, Katsumata, Noriyuki, Kanno, Junko, Hamajima, Takashi, Miyako, Kenichi, Ida, Shinobu, Hasegawa, Tomonobu

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SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7 von Narumi, Satoshi, Amano, Naoko, Ishii, Tomohiro, Katsumata, Noriyuki, Muroya, Koji, Adachi, Masanori, Toyoshima, Katsuaki, Tanaka, Yukichi, Fukuzawa, Ryuji, Miyako, Kenichi, Kinjo, Saori, Ohga, Shouichi, Ihara, Kenji, Inoue, Hirosuke, Kinjo, Tadamune, Hara, Toshiro, Kohno, Miyuki, Yamada, Shiro, Urano, Hironaka, Kitagawa, Yosuke, Tsugawa, Koji, Higa, Asumi, Miyawaki, Masakazu, Okutani, Takahiro, Kizaki, Zenro, Hamada, Hiroyuki, Kihara, Minako, Shiga, Kentaro, Yamaguchi, Tetsuya, Kenmochi, Manabu, Kitajima, Hiroyuki, Fukami, Maki, Shimizu, Atsushi, Kudoh, Jun, Shibata, Shinsuke, Okano, Hideyuki, Miyake, Noriko, Matsumoto, Naomichi, Hasegawa, Tomonobu

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Vitamin D deficiency rickets caused by improper lifestyle in Japanese children von Miyako, Kenichi, Kinjo, Saori, Kohno, Hitoshi

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Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan von Shibata, Nao, Numakura, Chikahiko, Hamajima, Takashi, Miyako, Kenichi, Fujiwara, Ikuma, Mori, Jun, Saitoh, Akihiko, Nagasaki, Keisuke

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Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities von Narumi, Satoshi, Nagasaki, Keisuke, Kiriya, Mitsuo, Uehara, Erika, Akiba, Kazuhisa, Tanase-Nakao, Kanako, Shimura, Kazuhiro, Abe, Kiyomi, Sugisawa, Chiho, Ishii, Tomohiro, Miyako, Kenichi, Hasegawa, Yukihiro, Maruo, Yoshihiro, Muroya, Koji, Watanabe, Natsuko, Nishihara, Eijun, Ito, Yuka, Kogai, Takahiko, Kameyama, Kaori, Nakabayashi, Kazuhiko, Hata, Kenichiro, Fukami, Maki, Shima, Hirohito, Kikuchi, Atsuo, Takayama, Jun, Tamiya, Gen, Hasegawa, Tomonobu

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In Vivo Determination of Replication Origins of Human Mitochondrial DNA by Ligation-mediated Polymerase Chain Reaction von Kang, Dongchon, Miyako, Kenichi, Kai, Yoichiro, Irie, Takashi, Takeshige, Koichiro

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Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene von KINJO, Saori, TAKEMOTO, Megumi, MIYAKO, Kenichi, KOHNO, Hitoshi, TANAKA, Toshiaki, KATSUMATA, Noriyuki

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MON-261 Investigation of GNAS1 Gene Mutations and Expression Patterns of Fibroblast Growth Factor 23 Protein in McCune-Albright Syndrome von Miyako, Kenichi, Mushimoto, Yuichi, Katsumata, Noriyuki

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