Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Akira Hishinuma"'
Autor:
Haruka Kishi, Teruo Jojima, Takahiko Kogai, Toshie Iijima, Eriko Ohira, Dai Tanuma, Sachiyo Konno, Kanako Kato, Atsumi Kezuka, Kazumi Akimoto, Junko Sakumoto, Akira Hishinuma, Takuya Tomaru, Noriko Makita, Isao Usui, Yoshimasa Aso
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3,
Externí odkaz:
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
Autor:
Tomoko Nagamine, Jaeduk Yoshimura Noh, Naoya Emoto, Takahito Kogai, Akira Hishinuma, Fumitaka Okajima, Hitoshi Sugihara
Publikováno v:
Thyroid Research, Vol 12, Iss 1, Pp 1-5 (2019)
Abstract Background Resistance to thyroid hormone (RTH) usually features a syndrome of inappropriate secretion of thyroid-stimulating hormone (SITSH) without suppression of the typical high thyroid hormone levels. However, some patients with RTH show
Externí odkaz:
https://doaj.org/article/cf87b809ebaf4401b709461282993686
Autor:
Yuka Okazaki, MD, Naoko Arata, MD, PhD, Nagayoshi Umehara, MD, PhD, Taisuke Yamauchi, MD, PhD, Junnichi Tajiri, MD, PhD, Akira Hishinuma, MD, PhD, Takahiko Kogai, MD, PhD, Takashi Idegami, MD, Atsuko Murashima, MD, PhD, Haruhiko Sago, MD, PhD
Publikováno v:
AACE Clinical Case Reports, Vol 6, Iss 2, Pp e94-e97 (2020)
ABSTRACT: Objective: Familial nonautoimmune hyperthyroidism (FNAH) is a rare disease. To date there are few, if any, reports of pregnancies in women with FNAH. Our objective here is to present such a case. Methods: Free thyroxine (free T4), free trii
Externí odkaz:
https://doaj.org/article/a347a56f7e8c4d2a9d65ca81261208ce
Autor:
Tetsuya Mizokami, MD, Akira Hishinuma, MD, PhD, Takahiko Kogai, MD, PhD, Katsuhiko Hamada, MD, PhD, Tetsushi Maruta, MD, Kiichiro Higashi, MD, PhD, Junichi Tajiri, MD, PhD
Publikováno v:
AACE Clinical Case Reports, Vol 3, Iss 2, Pp e176-e179 (2017)
ABSTRACT: Objective: To report a case of Pendred syndrome accompanied by hyperthyroidism that was treated with radioiodine. Pendred syndrome is an autosomal recessive disorder characterized by bilateral sensorineural hearing impairment, goiter, and i
Externí odkaz:
https://doaj.org/article/26751953e3484acaafa815adeda2ad0d
Autor:
Eijun Nishihara, Akira Hishinuma, Takahiko Kogai, Nami Takada, Mitsuyoshi Hirokawa, Shuji Fukata, Mitsuru Ito, Tomonori Yabuta, Mitsushige Nishikawa, Hirotoshi Nakamura, Nobuyuki Amino, Akira Miyauchi
Publikováno v:
Frontiers in Endocrinology, Vol 7 (2016)
Background: A germline mutation of KEAP1 gene was reported as a novel genetic abnormality associated with familial multinodular goiter. That report was limited, and the pathogenic features were not well established.Patient Findings: We report a 47-ye
Externí odkaz:
https://doaj.org/article/751f48196c2c46a78e4b44a254bf3237
Autor:
Toshio Kahara, Noboru Igarashi, Akira Hishinuma, Yuko Nakanishi, Akio Uchiyama, Atsuo Miwa, Shin Ishizawa, Yutaka Yamamoto, Hirofumi Noto, Hisashi Sumiya, Kazuhide Ishikura, Rika Usuda, Hiroyuki Iida
Publikováno v:
Case Reports in Endocrinology, Vol 2012 (2012)
Thyroglobulin gene mutation is a rare cause of congenital hypothyroidism, but thyroglobulin gene mutations are thought to be associated with thyroid cancer development. A 21-year-old Japanese man treated with levothyroxine for congenital hypothyroidi
Externí odkaz:
https://doaj.org/article/3ec2e25c906f48e8bad5311d78c25058
Autor:
Tsuyoshi Sekizuka, Mari Matsui, Kunikazu Yamane, Fumihiko Takeuchi, Makoto Ohnishi, Akira Hishinuma, Yoshichika Arakawa, Makoto Kuroda
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e25334 (2011)
The complete sequence of the plasmid pNDM-1_Dok01 carrying New Delhi metallo-β-lactamase (NDM-1) was determined by whole genome shotgun sequencing using Escherichia coli strain NDM-1_Dok01 (multilocus sequence typing type: ST38) and the transconjuga
Externí odkaz:
https://doaj.org/article/30cc6ead070d4fa8b886fdae17da3b78
Autor:
Chiho Sugisawa, Satoshi Narumi, Kanako Tanase-Nakao, Ayako Hoshiyama, Nami Suzuki, Hidemi Ohye, Miho Fukushita, Masako Matsumoto, Ai Yoshihara, Natsuko Watanabe, Kiminori Sugino, Akira Hishinuma, Jaeduk Yoshimura Noh, Ryohei Katoh, Matsuo Taniyama, Koichi Ito
Publikováno v:
Thyroid. 33:556-565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4f0fd3e7ecdde210382fd9360a356c9
https://doi.org/10.1089/thy.2022.0481
https://doi.org/10.1089/thy.2022.0481
Autor:
Misayo Matsuyama, Hirotake Sawada, Shinobu Inoue, Akira Hishinuma, Ryo Sekiya, Yuichiro Sato, Hiroshi Moritake
Publikováno v:
Clinical Pediatric Endocrinology. 31:185-191
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f186650cc36dbcba02af959eac28fa1
https://doi.org/10.1297/cpe.2022-0006
https://doi.org/10.1297/cpe.2022-0006
Autor:
Sachiyo Konno, Dai Tanuma, Eriko Ohira, Takahiko Kogai, Takuya Tomaru, Isao Usui, Teruo Jojima, Akira Hishinuma, Junko Sakumoto, Haruka Kishi, Kazumi Akimoto, Yoshimasa Aso, Atsumi Kezuka, Toshie Iijima, Noriko Makita, Kanako Kato
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Clinical Case Reports
Clinical Case Reports
Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3, but prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e17545ebfbbed64bca9bcb780ab639
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd