Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Junko Nishioka"'
Autor:
Miyuki Kitamura, Junko Nishioka, Takako Matsumoto, Satoko Umino, Atsuko Kawano, Reo Saiki, Yukari Tanaka, Shuichi Yatsuga
Publikováno v:
Endocrine and Metabolic Science, Vol 7, Iss , Pp 100119- (2022)
Objective: This study provided a rough estimate incidence of primary pediatric central diabetes insipidus (CDI) and examines the diagnostic factors between pediatric CDI and primary polydipsia (PP). Methods: We collected 27 patients with chief compla
Externí odkaz:
https://doaj.org/article/505944f2f4a447c1a499001fe82c3582
Autor:
Kikumi Ushijima-Fuchino, Yuko Koga, Satoko Umino, Junko Nishioka, Junichiro Araki, Shuichi Yatsuga, Yushiro Yamashita
Publikováno v:
Clinical Pediatric Endocrinology. 31:199-204
Autor:
Mayumi Matsumoto, Yukari Yamamoto, Yuji Sasada, Toshiki Mushino, Junko Nishioka, Naohito Fujishima, Hideaki Matsuura, Masanori Matsumoto
Publikováno v:
Japanese Journal of Transfusion and Cell Therapy. 66:590-597
Autor:
Yoshiko Yamazaki, Hideaki Matsuura, Risa Fuji, Mayumi Matsumoto, Akira Hosono, Yo Taniguchi, Hidemi Kimura, Ayami Kai, Takehiro Kohno, Junko Nishioka
Publikováno v:
Japanese Journal of Transfusion and Cell Therapy. 65:754-758
Autor:
Kazuhisa Chihara, Selin Elmaoğulları, Junko Nishioka, Takeshi Matsuda, Naoki Hattori, Akira Shimatsu
Publikováno v:
Journal of the Endocrine Society
Macro-TSH is mainly a complex of TSH with anti-TSH autoantibodies. Due to its large molecular size (>150 kDa), it accumulates in the circulation resulting in elevated serum TSH concentrations. Because the bioactivity of macro-TSH is low, treatment wi
Autor:
Tomoko Fuke, Akira Oka, Kanako Tanase-Nakao, Kazuhiko Nakabayashi, Tsutomu Ogata, Masayo Kagami, Junko Nishioka, Megumi Iwahashi-Odano, Yoshihiro Maruo, Akie Nakamura, Keiko Matsubara, Yoshiyuki Kobayashi, Seiji Sato, Hiroshi Suzumura, Satoshi Narumi, Maki Fukami, Yukihiro Hasegawa, Kazuki Yamazawa, Nobuyuki Murakami, Takanobu Inoue
Publikováno v:
Clinical Epigenetics
BackgroundSilver-Russell syndrome (SRS) is characterized by growth failure and dysmorphic features. Major (epi)genetic causes of SRS are loss of methylation on chromosome 11p15 (11p15 LOM) and maternal uniparental disomy of chromosome 7 (upd(7)mat).
Autor:
Kazuma Ikeda, Yuichi Hasegawa, Akihiro Takeshita, Yoshiki Okuyama, Shin-ichiro Fujiwara, Asashi Tanaka, Junko Nishioka, Kazuo Muroi, Mayumi Matsumoto, Kazuhiko Ikeda, Shuichi Kino, Keizo Fujino, Takehiro Kohno, Yoshiko Nakagawa, Shigeyoshi Makino, Akihiko Yokohama
Publikováno v:
Japanese Journal of Transfusion and Cell Therapy. 64:614-618
Autor:
Megumi Iwahashi-Odano, Keisuke Nagasaki, Maki Fukami, Junko Nishioka, Shuichi Yatsuga, Yumi Asakura, Masanori Adachi, Koji Muroya, Tomonobu Hasegawa, Satoshi Narumi, Iwahashi-Odano, Megumi, Nagasaki, Keisuke, Fukami, Maki, Nishioka, Junko, Yatsuga, Shuichi, Asakura, Yumi, Adachi, Masanori, Muroya, Koji, Hasegawa, Tomonobu, Narumi, Satoshi
Publikováno v:
Journal of Clinical Endocrinology & Metabolism; Nov2020, Vol. 105 Issue 11, p1-11, 11p
Autor:
Junko Nishioka, Shun Soneda, Maki Fukami, Yasuhiro Naiki, Hirohito Shima, Toshiaki Tanaka, Toshiya Kamiya, Akie Nakamura, Shinichiro Sano, Shuichi Yatsuga, Reiko Horikawa, Shuntaro Morikawa, Yuji Oto, Erina Suzuki, Sayaka Kawashima, Masayo Kagami, Yasuko Fujisawa, Tsutomu Ogata
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
We sequenced MKRN3, the major causative gene of central precocious puberty in Western countries, in 24 Japanese or Chinese patients and examined the DNA methylation and copy-number statuses of this gene in 19 patients. We identified no (epi)genetic d
Autor:
Tsutomu Ogata, Tomoko Fuke, Junko Nishioka, Masayo Kagami, Kazuki Yamazawa, Takanobu Inoue, Hideaki Yagasaki, Satoshi Narumi, Maki Fukami, Keiko Matsubara, Akira Oka, Akie Nakamura, Kazuhiko Nakabayashi
Publikováno v:
Journal of Medical Genetics
BackgroundRecently, a patient with maternal uniparental disomy of chromosome 16 (UPD(16)mat) presenting with Silver-Russell syndrome (SRS) phenotype was reported. SRS is characterised by growth failure and dysmorphic features.ObjectiveTo clarify the