Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Naoko Amano"'
Autor:
Yuko Shirouchi, Kazumi Kaihara, Tsunaki Sekita, Naoko Amano, Konosuke Nakayama, Kazunori Miyake, Hitoshi Abe, Hirotoshi Oinuma, Dai Maruyama
Publikováno v:
Cancer Medicine, Vol 13, Iss 16, Pp n/a-n/a (2024)
Abstract Background Immunofixation electrophoresis (IFE) is the standard method for confirming the presence of a monoclonal protein (M‐protein) at multiple myeloma (MM) diagnosis. IFE is also essential at assessment of complete response (CR) and st
Externí odkaz:
https://doaj.org/article/fe7b00a305a04d63ae57a9652c70c1c5
Publikováno v:
Current Opinion in Pediatrics; Aug2024, Vol. 36 Issue 4, p455-462, 7p
Autor:
Naoko Amano, Satoshi Narumi, Katsuya Aizu, Mari Miyazawa, Kohji Okamura, Hirofumi Ohashi, Noriyuki Katsumata, Tomohiro Ishii, Tomonobu Hasegawa
Publikováno v:
Journal of Clinical Endocrinology & Metabolism; Mar2024, Vol. 109 Issue 3, p641-648, 8p
Autor:
Il Tae Hwang, Yusuke Mizuno, Naoko Amano, Hye Jin Lee, Young Suk Shim, Hyo‐Kyoung Nam, Young‐Jun Rhie, Seung Yang, Kee‐Hyoung Lee, Tomonobu Hasegawa, Min Jae Kang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background C‐type natriuretic peptide (CNP, NPPC) and its receptor, natriuretic peptide receptor‐B (NPR‐B, NPR2), are critical for endochondral ossification. A monoallelic NPR2 mutation has been suggested to mildly impair long bone gro
Externí odkaz:
https://doaj.org/article/a293c706d6ac41e5b81f16426a87aae7
Autor:
Naoko Amano1,2 naokoam@z8.keio.jp, Hiroshi Kitoh3, Satoshi Narumi4, Gen Nishimura5, Tomonobu Hasegawa1
Publikováno v:
Clinical Pediatric Endocrinology. 2020, Vol. 29 Issue 3, p99-103. 5p.
Autor:
Akari Nakamura-Utsunomiya, Yukihiro Hasegawa, Kei Takasawa, Tomohiro Ishii, Tomonobu Hasegawa, Toshihiro Tajima, Naoko Amano, Shinobu Ida
Publikováno v:
Endocrine Journal. 69:75-83
To manage of 21-hydroxylase deficiency (21-OHD), transition medicine from pediatric to adult health care is an important process and requires individually optimized approaches. We sent cross-sectional questionnaire surveys on the current status of tr
Autor:
Hirohito Shima, Mie Hayashi, Takashi Tachibana, Makoto Oshiro, Naoko Amano, Tomohiro Ishii, Hidenori Haruna, Maki Igarashi, Masafumi Kon, Ryuji Fukuzawa, Yukichi Tanaka, Maki Fukami, Tomonobu Hasegawa, Satoshi Narumi
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206184 (2018)
BACKGROUND:MIRAGE syndrome, a congenital multisystem disorder due to pathogenic SAMD9 variants, describes a constellation of clinical features including 46,XY disorders of sex development (DSD), small for gestational age (SGA) and adrenal insufficien
Externí odkaz:
https://doaj.org/article/16e20c22f7da4c5fbb796d884bad9e82
Publikováno v:
Clinical Pediatric Endocrinology. 29:99-103
Acromesomelic dysplasia, type Maroteaux (AMDM) is a congenital bone dysplasia characterized by disproportionate, acromesomelic shortening of the limbs and mild spondylar dysplasia. AMDM is caused by biallelic loss-of-function mutations in NPR2 encodi
Autor:
Toshihide Kawai, Kumiko Tanaka, Hajime Tanaka, Takeshi Katsuki, Nobuyuki Shimozawa, Naoko Amano, Tomohide Adachi
Publikováno v:
Endocrine Journal. 67:655-658
Adrenoleukodystrophy (ALD) is an X-linked disorder caused by a hemizygous mutation of the ABCD1 gene. Patients with ALD show progressive central nervous system demyelination and primary adrenal insufficiency. In Japan, most reported ALD cases were ch
Autor:
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
Publikováno v:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 31(3)
Congenital adrenal hyperplasia is a category of disorders characterized by impaired adrenocortical steroidogenesis. The most frequent disorder of congenital adrenal hyperplasia is 21-hydroxylase deficiency, which is caused by pathogenic variants of