Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan
Shibata, Nao, Numakura, Chikahiko, Hamajima, Takashi, Miyako, Kenichi, Fujiwara, Ikuma, Mori, Jun, Saitoh, Akihiko, Nagasaki, Keisuke
Published in Endocrine Journal (01.01.2024)
Published in Endocrine Journal (01.01.2024)
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Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version
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
Published in Diabetology international (01.10.2024)
Published in Diabetology international (01.10.2024)
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Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
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
Published in Kidney international reports (01.01.2019)
Published in Kidney international reports (01.01.2019)
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Age-Related Clinical Characteristics of Isolated Congenital Unilateral Absence of a Pulmonary Artery
Koga, Hiroshi, Hidaka, Tomoko, Miyako, Kenichi, Suga, Naohiro, Takahashi, Noboru
Published in Pediatric cardiology (01.11.2010)
Published in Pediatric cardiology (01.11.2010)
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A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency
Kawano, Atsuko, Kohno, Hitoshi, Miyako, Kenichi
Published in Clinical Pediatric Endocrinology (01.04.2014)
Published in Clinical Pediatric Endocrinology (01.04.2014)
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Improving circulatory disturbance in transient abnormal myelopoiesis
Koga, Hiroshi, Miyako, Kenichi, Suga, Naohiro, Hidaka, Tomoko, Takahashi, Noboru
Published in Journal of pediatric hematology/oncology (01.05.2012)
Published in Journal of pediatric hematology/oncology (01.05.2012)
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Journal Article
PAPA-1 Is a Nuclear Binding Partner of IGFBP-2 and Modulates Its Growth-Promoting Actions
Miyako, Kenichi, Cobb, Laura J, Francis, Malik, Huang, Alden, Peng, Bonnie, Pintar, John E, Ariga, Hiroyoshi, Cohen, Pinchas
Published in Molecular endocrinology (Baltimore, Md.) (01.02.2009)
Published in Molecular endocrinology (Baltimore, Md.) (01.02.2009)
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Predisposition to Subdural Hemorrhage in X-Linked Myotubular Myopathy
Koga, Hiroshi, MD, Miyako, Kenichi, MD, PhD, Suga, Naohiro, MD, PhD, Hidaka, Tomoko, MD, Takahashi, Noboru, MD, PhD
Published in Pediatric neurology (01.05.2012)
Published in Pediatric neurology (01.05.2012)
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Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus
Miyako, Kenichi, Yamaguchi, Yui, Sakemi, Yoshihiro, Suga, Naohiro, Utsunomiya, Rina, Takahashi, Noboru
Published in Pediatrics international (01.04.2011)
Published in Pediatrics international (01.04.2011)
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A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency
Atsuko Kawano, Hitoshi Kohno, Kenichi Miyako
Published in Clinical Pediatric Endocrinology (01.04.2014)
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Published in Clinical Pediatric Endocrinology (01.04.2014)
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Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene
KINJO, Saori, TAKEMOTO, Megumi, MIYAKO, Kenichi, KOHNO, Hitoshi, TANAKA, Toshiaki, KATSUMATA, Noriyuki
Published in Endocrine Journal (01.10.2004)
Published in Endocrine Journal (01.10.2004)
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Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome
Tanaka, Wataru, Oyama, Noriko, Makimura, Mika, Miyako, Kenichi
Published in Pediatrics international (01.01.2023)
Published in Pediatrics international (01.01.2023)
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Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus
MIYAKO, Kenichi, KOHNO, Hitoshi, IHARA, Kenji, KUROMARU, Ryuichi, MATSUURA, Nobuo, HARA, Toshiro
Published in Endocrine Journal (01.10.2004)
Published in Endocrine Journal (01.10.2004)
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SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7
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
Published in Nature genetics (01.07.2016)
Published in Nature genetics (01.07.2016)
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Journal Article
Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan
Shibata, Nao, Numakura, Chikahiko, Hamajima, Takashi, Miyako, Kenichi, Fujiwara, Ikuma, Mori, Jun, Saitoh, Akihiko, Nagasaki, Keisuke
Published in Endocrine Journal (2024)
Published in Endocrine Journal (2024)
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Journal Article
Case Report: Adjuvant Therapy with a High Dose of Mitotane for Adrenocortical Carcinoma in a 4-year-old Boy
Goto, Takako, Miyako, Kenichi, Kuromaru, Ryuichi, Ihara, Kenji, Torisu, Hiroyuki, Sanefuji, Masafumi, Nagamatsu, Rie, Hara, Toshiro
Published in Clinical Pediatric Endocrinology (01.01.2008)
Published in Clinical Pediatric Endocrinology (01.01.2008)
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Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited
Ishii, Tomohiro, Tajima, Toshihiro, Kashimada, Kenichi, Mukai, Tokuo, Tanahashi, Yusuke, Katsumata, Noriyuki, Kanno, Junko, Hamajima, Takashi, Miyako, Kenichi, Ida, Shinobu, Hasegawa, Tomonobu
Published in The journal of clinical endocrinology and metabolism (01.11.2020)
Published in The journal of clinical endocrinology and metabolism (01.11.2020)
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