Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yuichi Miyakawa"'
Autor:
Shigeru Takishima, Tomohiro Morio, Takeru Yamauchi, Akito Sutani, Atsumi Hosokawa-Tsuji, Ryuichi Nakagawa, Yuichi Miyakawa, Maki Gau, Yoko Saito, Yohei Matsubara, Kei Takasawa, Kenichi Kashimada
Publikováno v:
Clinical Pediatric Endocrinology
In Japan, since the introduction of newborn screening for congenital adrenal hyperplasia in 1989, most patients with 21-hydroxylase deficiency (21OHD) have been treated with glucocorticoid from the neonatal period (1, 2). Although early initiation of
Autor:
Akito Sutani1, Yuichi Miyakawa1, Atsumi Tsuji-Hosokawa1, Risa Nomura1, Ryuichi Nakagawa1, Keisuke Nakajima1,2, Mitsue Maru1,3, Yuki Aoki1, Kei Takasawa1, Masatoshi Takagi1, Kohsuke Imai1, Kenichi Kashimada1 kkashimada.ped@tmd.ac.jp, Tomohiro Morio1
Publikováno v:
Clinical Pediatric Endocrinology. Oct2019, Vol. 28 Issue 4, p105-112. 8p.
Autor:
Risa Nomura, Ryuichi Nakagawa, Masatoshi Takagi, Tomohiro Morio, Keisuke Nakajima, Kei Takasawa, Kohsuke Imai, Kenichi Kashimada, Yuichi Miyakawa, Yuki Aoki, Mitsue Maru, Atsumi Tsuji-Hosokawa, Akito Sutani
Publikováno v:
Clinical Pediatric Endocrinology
In addition to malignant diseases, hematopoietic stem cell transplantation (HSCT) is also a vital option as a curative therapy for non-malignant diseases, such as immunodeficiency, and other hematological disorders. Not only for malignant diseases, b
Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation
Autor:
Tomohiro Morio, Kenichi Kashimada, Yoko Saito, Atsuko Taki, Ryuichi Nakagawa, Tsunanori Shidei, Eriko Adachi, Kei Takasawa, Akito Sutani, Maki Gau, Yuichi Miyakawa
Publikováno v:
Clinical endocrinologyREFERENCES. 94(6)
Background The most severe forms of congenital hyperinsulinism (CHI) are caused by inactivating mutations of two KATP channel genes, KCNJ11 and ABCC8. Unresponsiveness to diazoxide and need for subtotal pancreatectomy can usually be predicted by gene
Autor:
Nakagawa R, Yuichi Miyakawa, Akito Sutani, Keisuke Nakajima, Kei Takasawa, Yuki Aoki, aru M, Daisuke Tomizawa, ashimada K, Atsumi Hosokawa-Tsuji, Tomohiro Morio
Publikováno v:
Endocrine. 61:76-82
Hematopoietic stem cell transplantation (HSCT) is a curative treatment for life-threatening malignancies and related diseases. Recently, the long-term prognosis of HSCT during childhood has greatly improved; however, the late adverse effects of HSCT
Autor:
Hiroshi Mochizuki, Yukihiro Hasegawa, Kenji Ihara, Sumito Dateki, Ichiro Yokota, Sinichiro Sano, Hironori Kobayashi, Hotaka Kamasaki, Yoshiaki Ohtsu, Yuichi Miyakawa, Mari Satoh, Yohei Matsubara, Kazuteru Kitsuda, Kei Takasawa, Kenichi Kashimada
Publikováno v:
Endocrine journal. 66(3)
Pseudohypoparathyroidism type 1A (PHP1A) is characterized by resistance to multiple hormones, the Albright Hereditary Osteodystrophy phenotype, obesity, and developmental delay. Developmental delay usually appears prior to hypocalcemia due to parathy
Autor:
Yoko Saito, Kei Takasawa, Maki Gau, Takeru Yamauchi, Ryuichi Nakagawa, Yuichi Miyakawa, Akito Sutani, Atsumi Hosokawa-Tsuji, Shigeru Takishima, Yohei Matsubara, Tomohiro Morio, Kenichi Kashimada
Publikováno v:
Clinical Pediatric Endocrinology; 2021, Vol. 30 Issue 4, p155-161, 7p
Publikováno v:
Acta Diabetologica. 53:507-510
Autor:
Tsuyoshi Shirai, Tomohiro Morio, Atsumi Tsuji-Hosokawa, Kei Takasawa, Kenichi Kashimada, Chikahiko Numakura, Atsushi Hijikata, Risa Nomura, Yoshihiro Ogawa, Yuichi Miyakawa
Publikováno v:
Pediatric diabetes. 18(8)
BACKGROUND Defects of the insulin receptor gene ( INSR ) cause wide spectra of congenital insulin resistance. Monoallelic defects result in milder insulin-resistant diabetes mellitus with acanthosis nigricans (IRAN, type A). Whereas, leprechaunism (D
Publikováno v:
Journal of the Japan Veterinary Medical Association. 61:386-389