Discovery of GnIH and Its Role in Hypothyroidism-Induced Delayed Puberty
Tsutsui, Kazuyoshi, Son, You Lee, Kiyohara, Mika, Miyata, Ichiro
Published in Endocrinology (Philadelphia) (01.01.2018)
Published in Endocrinology (Philadelphia) (01.01.2018)
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A case of neuronal ceroid lipofuscinosis type 8 associated with central precocious puberty
Saito, Maki, Hirano, Daishi, Kobayashi, Hiroshi, Kosaki, Kenjiro, Miyata, Ichiro
Published in Pediatrics international (01.03.2021)
Published in Pediatrics international (01.03.2021)
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Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance
Hosoe, Jun, Kadowaki, Hiroko, Miya, Fuyuki, Aizu, Katsuya, Kawamura, Tomoyuki, Miyata, Ichiro, Satomura, Kenichi, Ito, Takeru, Hara, Kazuo, Tanaka, Masaki, Ishiura, Hiroyuki, Tsuji, Shoji, Suzuki, Ken, Takakura, Minaka, Boroevich, Keith A, Tsunoda, Tatsuhiko, Yamauchi, Toshimasa, Shojima, Nobuhiro, Kadowaki, Takashi
Published in Diabetes (New York, N.Y.) (01.10.2017)
Published in Diabetes (New York, N.Y.) (01.10.2017)
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Novel biallelic splice-site BBS1 variants in Bardet–Biedle syndrome: a case report of the first Japanese patient
Katagiri, Satoshi, Hosono, Katsuhiro, Hayashi, Takaaki, Murai, Noriyuki, Wake, Eiichi, Miyata, Ichiro, Mizobuchi, Kei, Kurata, Kentaro, Matsuura, Tomokazu, Nakano, Tadashi, Hotta, Yoshihiro
Published in Documenta ophthalmologica (01.08.2020)
Published in Documenta ophthalmologica (01.08.2020)
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Essential Amino Acid Intake Is Required for Sustaining Serum Insulin-like Growth Factor-I Levels but Is Not Necessarily Needed for Body Growth
Nishi, Hiroki, Uchida, Kaito, Saito, Maki, Yamanaka, Daisuke, Nagata, Haruka, Tomoshige, Hinako, Miyata, Ichiro, Ito, Koichi, Toyoshima, Yuka, Takahashi, Shin-Ichiro, Hakuno, Fumihiko, Takenaka, Asako
Published in Cells (Basel, Switzerland) (02.05.2022)
Published in Cells (Basel, Switzerland) (02.05.2022)
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Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features
Ono, Erina, Ariga, Masamichi, Oshima, Sakiko, Hayakawa, Mika, Imai, Masayuki, Ochiai, Yukikatsu, Mochizuki, Hiroshi, Namba, Noriyuki, Ozono, Keiichi, Miyata, Ichiro
Published in Clinical Pediatric Endocrinology (01.01.2016)
Published in Clinical Pediatric Endocrinology (01.01.2016)
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Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols
Sato, Naoko, Hasegawa, Tomonobu, Hasegawa, Yukihiro, Arisaka, Osamu, Ozono, Keiichi, Amemiya, Shin, Kikuchi, Toru, Tanaka, Hiroyuki, Harada, Shohei, Miyata, Ichiro, Tanaka, Toshiaki
Published in Clinical Pediatric Endocrinology (2015)
Published in Clinical Pediatric Endocrinology (2015)
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Atypical clinical features of children with central nervous system tumor: Delayed diagnosis and switch in handedness
Yokoi, Kentaro, Yamaoka, Masayoshi, Miyata, Ichiro, Nonaka, Yuichiro, Yuza, Yuki, Kawata, Shoko, Akiyama, Masaharu, Yanagisawa, Takaaki, Ida, Hiroyuki
Published in Pediatrics international (01.09.2016)
Published in Pediatrics international (01.09.2016)
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A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1
Tsunogai, Toshiki, Miyata, Ichiro, Kotake, Saori, Matsuura, Ryuki, Takagi, Ken, Nanba, Hiroyuki, Takahata, Noriko, Tajima, Toshihiro, Wada, Yasuyuki
Published in Clinical Pediatric Endocrinology (01.01.2016)
Published in Clinical Pediatric Endocrinology (01.01.2016)
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Successful Intrauterine Therapy for Fetal Goitrous Hypothyroidism during Late Gestation
MIYATA, Ichiro, ABE-GOTYO, Noriko, TAJIMA, Asako, YOSHIKAWA, Hideki, TERAMOTO, Satoshi, SEO, Masami, KANNO, Kei-ichi, SUGIURA, Kentaro, TANAKA, Tadao, ETO, Yoshikatsu
Published in ENDOCRINE JOURNAL (2007)
Published in ENDOCRINE JOURNAL (2007)
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Diagnostic Usefulness of 3 Tesla MRI of the Brain for Cushing Disease in a Child
Ono, Erina, Ozawa, Ayako, Matoba, Kaori, Motoki, Takanori, Tajima, Asako, Miyata, Ichiro, Ito, Junko, Inoshita, Naoko, Yamada, Syozo, Ida, Hiroyuki
Published in Clinical Pediatric Endocrinology (2011)
Published in Clinical Pediatric Endocrinology (2011)
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A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1
Toshiki Tsunogai, Ichiro Miyata, Saori Kotake, Ryuki Matsuura, Ken Takagi, Hiroyuki Nanba, Noriko Takahata, Toshihiro Tajima, Yasuyuki Wada
Published in Clinical Pediatric Endocrinology (01.07.2016)
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Published in Clinical Pediatric Endocrinology (01.07.2016)
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Cloning and Characterization of a Short Variant of the Corticotropin-Releasing Factor Receptor Subtype from Rat Amygdala
Miyata, Ichiro, Shiota, Chiyo, Ikeda, Yoko, Oshida, Yuichi, Chaki, Shigeyuki, Okuyama, Shigeru, Inagami, Tadashi
Published in Biochemical and biophysical research communications (24.03.1999)
Published in Biochemical and biophysical research communications (24.03.1999)
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A Case of Allgrove Syndrome with a Novel IVS7 +1 G>A Mutation of The AAAS Gene
Satoru Ikemoto, Ken Sakurai, Naruo Kuwashima, Yoshihiro Saito, Ichiro Miyata, Noriyuki Katsumata, Hiroyuki Ida
Published in Clinical Pediatric Endocrinology (01.01.2012)
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Published in Clinical Pediatric Endocrinology (01.01.2012)
Journal Article
Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations
Tanase-Nakao, Kanako, Miyata, Ichiro, Terauchi, Ayako, Saito, Maki, Wada, Seiji, Hasegawa, Tomonobu, Narumi, Satoshi
Published in Hormone research in paediatrics (01.01.2018)
Published in Hormone research in paediatrics (01.01.2018)
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