Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists
Takasawa, Kei, Nakamura-Utsunomiya, Akari, Amano, Naoko, Ishii, Tomohiro, Hasegawa, Tomonobu, Hasegawa, Yukihiro, Tajima, Toshihiro, Ida, Shinobu
Published in ENDOCRINE JOURNAL (01.01.2022)
Published in ENDOCRINE JOURNAL (01.01.2022)
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Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan
Yatsuga, Shuichi, Amano, Naoko, Nakamura-Utsunomiya, Akari, Kobayashi, Hironori, Takasawa, Kei, Nagasaki, Keisuke, Nakamura, Akie, Nishigaki, Satsuki, Numakura, Chikahiko, Fujiwara, Ikuma, Minamitani, Kanshi, Hasegawa, Tomonobu, Tajima, Toshihiro
Published in ENDOCRINE JOURNAL (01.01.2020)
Published in ENDOCRINE JOURNAL (01.01.2020)
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Prevalence and associated factors of foot and ankle pain among nurses at a university hospital in Japan : A cross-sectional study
Tojo, Maki, Yamaguchi, Satoshi, Amano, Naoko, Ito, Akemi, Futono, Machiko, Sato, Yasunori, Naka, Takako, Kimura, Seiji, Sadamasu, Aya, Akagi, Ryuichiro, Ohtori, Seiji
Published in Journal of Occupational Health (01.03.2018)
Published in Journal of Occupational Health (01.03.2018)
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MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency
Shima, Hirohito, Hayashi, Mie, Tachibana, Takashi, Oshiro, Makoto, Amano, Naoko, Ishii, Tomohiro, Haruna, Hidenori, Igarashi, Maki, Kon, Masafumi, Fukuzawa, Ryuji, Tanaka, Yukichi, Fukami, Maki, Hasegawa, Tomonobu, Narumi, Satoshi
Published in PloS one (07.11.2018)
Published in PloS one (07.11.2018)
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Clinical and Immunological Analyses of Ten Patients with MIRAGE Syndrome
Mitsui-Sekinaka, Kanako, Narumi, Satoshi, Sekinaka, Yujin, Uematsu, Kenji, Yoshida, Yusuke, Amano, Naoko, Shima, Hirohito, Hasegawa, Tomonobu, Nonoyama, Shigeaki
Published in Journal of clinical immunology (01.04.2021)
Published in Journal of clinical immunology (01.04.2021)
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Genetic defects in pediatric-onset adrenal insufficiency in Japan
Amano, Naoko, Narumi, Satoshi, Hayashi, Mie, Takagi, Masaki, Imai, Kazuhide, Nakamura, Toshiro, Hachiya, Rumi, Sasaki, Goro, Homma, Keiko, Ishii, Tomohiro, Hasegawa, Tomonobu
Published in European journal of endocrinology (01.08.2017)
Published in European journal of endocrinology (01.08.2017)
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Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature
Vasques, Gabriela A, Amano, Naoko, Docko, Ana J, Funari, Mariana F. A, Quedas, Elisangela P. S, Nishi, Mirian Y, Arnhold, Ivo J. P, Hasegawa, Tomonobu, Jorge, Alexander A. L
Published in The journal of clinical endocrinology and metabolism (01.10.2013)
Published in The journal of clinical endocrinology and metabolism (01.10.2013)
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A 29-year-old patient with adrenoleukodystrophy presenting with Addison’s disease
Tanaka, Hajime, Amano, Naoko, Tanaka, Kumiko, Katsuki, Takeshi, Adachi, Tomohide, Shimozawa, Nobuyuki, Kawai, Toshihide
Published in Endocrine Journal (01.01.2020)
Published in Endocrine Journal (01.01.2020)
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Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)
Ishii, Tomohiro, Kashimada, Kenichi, Amano, Naoko, Takasawa, Kei, Nakamura-Utsunomiya, Akari, Yatsuga, Shuichi, Mukai, Tokuo, Ida, Shinobu, Isobe, Mitsuhisa, Fukushi, Masaru, Satoh, Hiroyuki, Yoshino, Kaoru, Otsuki, Michio, Katabami, Takuyuki, Tajima, Toshihiro
Published in Clinical Pediatric Endocrinology (01.01.2022)
Published in Clinical Pediatric Endocrinology (01.01.2022)
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Heterozygous defects in PAX6 gene and congenital hypopituitarism
Takagi, Masaki, Nagasaki, Keisuke, Fujiwara, Ikuma, Ishii, Tomohiro, Amano, Naoko, Asakura, Yumi, Muroya, Koji, Hasegawa, Yukihiro, Adachi, Masanori, Hasegawa, Tomonobu
Published in European journal of endocrinology (01.01.2015)
Published in European journal of endocrinology (01.01.2015)
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Pubertal and Adult Testicular Functions in Nonclassic Lipoid Congenital Adrenal Hyperplasia: A Case Series and Review
Ishii, Tomohiro, Hori, Naoaki, Amano, Naoko, Aya, Misaki, Shibata, Hirotaka, Katsumata, Noriyuki, Hasegawa, Tomonobu
Published in Journal of the Endocrine Society (01.07.2019)
Published in Journal of the Endocrine Society (01.07.2019)
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Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism
Takagi, Masaki, Ishii, Tomohiro, Inokuchi, Mikako, Amano, Naoko, Narumi, Satoshi, Asakura, Yumi, Muroya, Koji, Hasegawa, Yukihiro, Adachi, Masanori, Hasegawa, Tomonobu
Published in PloS one (24.09.2012)
Published in PloS one (24.09.2012)
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Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan
Yatsuga, Shuichi, Amano, Naoko, Nakamura-Utsunomiya, Akari, Kobayashi, Hironori, Takasawa, Kei, Nagasaki, Keisuke, Nakamura, Akie, Nishigaki, Satsuki, Numakura, Chikahiko, Fujiwara, Ikuma, Minamitani, Kanshi, Hasegawa, Tomonobu, Toshihiro, Tajima
Published in Endocrine Journal (2020)
Published in Endocrine Journal (2020)
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Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)
Tomohiro Ishii, Kenichi Kashimada, Naoko Amano, Kei Takasawa, Akari Nakamura-Utsunomiya, Shuichi Yatsuga, Tokuo Mukai, Shinobu Ida, Mitsuhisa Isobe, Masaru Fukushi, Hiroyuki Satoh, Kaoru Yoshino, Michio Otsuki, Takuyuki Katabami, Toshihiro Tajima
Published in Clinical Pediatric Endocrinology (01.07.2022)
Published in Clinical Pediatric Endocrinology (01.07.2022)
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A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta
Takagi, Masaki, Ishii, Tomohiro, Barnes, Aileen M, Weis, Maryann, Amano, Naoko, Tanaka, Mamoru, Fukuzawa, Ryuji, Nishimura, Gen, Eyre, David R, Marini, Joan C, Hasegawa, Tomonobu
Published in PloS one (15.05.2012)
Published in PloS one (15.05.2012)
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IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients
Kato, Fumiko, Hamajima, Takashi, Hasegawa, Tomonobu, Amano, Naoko, Horikawa, Reiko, Nishimura, Gen, Nakashima, Shinichi, Fuke, Tomoko, Sano, Shinichirou, Fukami, Maki, Ogata, Tsutomu
Published in Clinical endocrinology (Oxford) (01.05.2014)
Published in Clinical endocrinology (Oxford) (01.05.2014)
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Role of NPR2 mutation in idiopathic short stature: Identification of two novel mutations
Hwang, Il Tae, Mizuno, Yusuke, Amano, Naoko, Lee, Hye Jin, Shim, Young Suk, Nam, Hyo‐Kyoung, Rhie, Young‐Jun, Yang, Seung, Lee, Kee‐Hyoung, Hasegawa, Tomonobu, Kang, Min Jae
Published in Molecular genetics & genomic medicine (01.03.2020)
Published in Molecular genetics & genomic medicine (01.03.2020)
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