Zobrazeno 1 - 10
of 136
pro vyhledávání: '"Haruo Mizuno"'
Autor:
Naoya Yamaguchi, Atsushi Suzuki, Aya Yoshida, Tatsushi Tanaka, Kohei Aoyama, Hisashi Oishi, Yuichiro Hara, Tomoo Ogi, Izuki Amano, Satomi Kameo, Noriyuki Koibuchi, Yasuhiro Shibata, Shinya Ugawa, Haruo Mizuno, Shinji Saitoh
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract SLC26A4 is a known iodide transporter, and is localized at the apical membrane of thyrocytes. Previously, we reported that SLC26A7 is also involved in iodide transport and that Slc26a7 is a novel causative gene for congenital hypothyroidism.
Externí odkaz:
https://doaj.org/article/e96f5e5bc5174803af6db215698f5947
Autor:
Yuki Hosokawa, Shinji Higuchi, Rie Kawakita, Ikue Hata, Tatsuhiko Urakami, Tsuyoshi Isojima, Kei Takasawa, Yohei Matsubara, Haruo Mizuno, Yoshihiro Maruo, Katsuyuki Matsui, Katsuya Aizu, Kazuhiko Jinno, Shunsuke Araki, Yasuko Fujisawa, Koji Osugi, Chikako Tono, Yasuhiro Takeshima, Tohru Yorifuji
Publikováno v:
Journal of Diabetes Investigation, Vol 10, Iss 6, Pp 1586-1589 (2019)
Abstract Aims/Introduction Glucokinase–maturity‐onset diabetes of the young (GCK‐MODY; also known as MODY2) is a benign hyperglycemic condition, which generally does not require medical interventions. The only known exception is increased birth
Externí odkaz:
https://doaj.org/article/7c67130c05d84e4e82d9f7eb89699c36
Autor:
Hideyuki Iwayama, Tatsushi Tanaka, Kohei Aoyama, Masaharu Moroto, Shinsuke Adachi, Yasuko Fujisawa, Hiroki Matsuura, Kyoko Takano, Haruo Mizuno, Akihisa Okumura
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Monocarboxylate transporter 8 (MCT8) is a thyroid hormone transmembrane transporter protein. MCT8 deficiency induces severe X-linked psychomotor retardation. Previous reports have documented delayed myelination in the central white matter
Externí odkaz:
https://doaj.org/article/fd5dc365cd194056a2de83514ecce128
Autor:
Sonoko Sakata, Satoshi Okada, Kohei Aoyama, Keiichi Hara, Chihiro Tani, Reiko Kagawa, Akari Utsunomiya-Nakamura, Shinichiro Miyagawa, Tsutomu Ogata, Haruo Mizuno, Masao Kobayashi
Publikováno v:
Frontiers in Genetics, Vol 8 (2017)
We report a Japanese female patient presenting with classic features of CHARGE syndrome, including choanal atresia, growth and development retardation, ear malformations, genital anomalies, multiple endocrine deficiency, and unilateral facial nerve p
Externí odkaz:
https://doaj.org/article/b1fd17da7c654994b3eb9f6be9be2674
Autor:
Aya Yoshida, Kohei Aoyama, Naoya Yamaguchi, Atsushi Suzuki, Haruo Mizuno, Hayato Tada, Shinji Saitoh
Publikováno v:
Clinical Pediatric Endocrinology. 32:114-118
Autor:
Atsushi Ishida1 ishida-atsushi@tajimi-hospital.jp, Haruo Mizuno2, Kohei Aoyama3, Shiori Sasaki1,4, Yutaka Negishi1,3, Takeshi Arakawa1, Takayasu Mori5
Publikováno v:
Clinical Pediatric Endocrinology. 2022, Vol. 31 Issue 1, p44-49. 6p.
Autor:
Haruo Mizuno, Kohei Aoyama, Shiori Sasaki, Takeshi Arakawa, Yutaka Negishi, Atsushi Ishida, Takayasu Mori
Publikováno v:
Clinical Pediatric Endocrinology
X-linked nephrogenic diabetes insipidus (NDI) is caused by variations in arginine vasopressin receptor 2 (AVPR2). Some patients show partial resistance to arginine vasopressin (AVP). A 19-month-old Japanese boy presented with polydipsia since infancy
Autor:
Katsuya Aizu, Tatsuhiko Urakami, Chikako Tono, Tsuyoshi Isojima, Yuki Hosokawa, Yohei Matsubara, Ikue Hata, Koji Osugi, Yasuko Fujisawa, Rie Kawakita, Shunsuke Araki, Yasuhiro Takeshima, Kei Takasawa, Kazuhiko Jinno, Shinji Higuchi, Tohru Yorifuji, Yoshihiro Maruo, Katsuyuki Matsui, Haruo Mizuno
Publikováno v:
Journal of Diabetes Investigation
Journal of Diabetes Investigation, Vol 10, Iss 6, Pp 1586-1589 (2019)
Journal of Diabetes Investigation, Vol 10, Iss 6, Pp 1586-1589 (2019)
Aims/Introduction Glucokinase–maturity‐onset diabetes of the young (GCK‐MODY; also known as MODY2) is a benign hyperglycemic condition, which generally does not require medical interventions. The only known exception is increased birthweight an
Autor:
Hiroki Miura, Haruo Mizuno, Toya Kono, Tetsushi Yoshikawa, Yoshiki Kawamura, Kei Kozawa, Daijiro Suzuki
Publikováno v:
Pediatric Infectious Disease Journal. 41:78-79
Here, we present a previously healthy adolescent with aseptic meningitis without skin rash caused by varicella vaccine derived from the Oka/Biken strain; the patient received a single dose of varicella vaccine at 1 year of age. Pediatricians should b
Autor:
Seiji Fukumoto, Keiichi Ozono, Koji Oba, Haruo Mizuno, Hirokazu Tsukahara, Hirofumi Nakayama, Keisuke Nagasaki, Satoshi Kusuda, Yosikazu Nakamura, Sachiko Kitanaka, Toshimi Michigami, Satomi Koyama, Yukihiro Hasegawa, Ikuma Fujiwara, Kenji Ihara, Noriyuki Takubo, Tohru Yorifuji, Kosei Hasegawa, Taichi Kitaoka, Toshiaki Shimizu, Yuko Sakamoto, Yusuke Tanahashi, Takuo Kubota
Publikováno v:
Endocrine Journal. 65:593-599
There is concern that vitamin D deficiency is prevalent among children in Japan as well as worldwide. We conducted a nationwide epidemiologic survey of symptomatic vitamin D deficiency to observe its incidence rate among Japanese children. A question