Výsledky vyhledávání - "Akiko, Furuya"

Akademický článek

Awe, fear, and ethics expressed in The Tale of Genji.

Autor: Akiko FURUYA

Publikováno v: Bulletin of Daito Bunka University. Humanities / Daito Bunka Daigaku Kiyo. Jimbun Kagaku. 2024, Vol. 62, p1-20. 20p.

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A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression

Autor: Takahide Kokumai, Koichi Yano, Yoshiya Ito, Kumihiro Matsuo, Shigeru Suzuki, Atsushi Kobayashi, Akimasa Okuno, Kenji Fujieda, Hiroshi Azuma, Akiko Furuya, Yusuke Tanahashi, Tokuo Mukai, Osamu Ueda

Publikováno v: European Journal of Endocrinology. 185:1-12

Background POU1F1 encodes both PIT-1α, which plays pivotal roles in pituitary development and GH, PRL and TSHB expression, and the alternatively spliced isoform PIT-1β, which contains an insertion of 26-amino acids (β-domain) in the transactivatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6330c08426c2edd0287654e3cabfa263
https://doi.org/10.1530/eje-20-1313

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Increase in doses of levothyroxine at the age of 3 years and above is useful for distinguishing transient and permanent congenital hypothyroidism

Autor: Hiroshi Azuma, Akiko Furuya, Hinako Yamamura, Shigeru Suzuki, Takahide Kokumai, Yusuke Tanahashi

Publikováno v: Clinical Pediatric Endocrinology

There are no recommended diagnostic criteria for transient congenital hypothyroidism (CH) during early childhood. In this study, we aimed to identify the factors that distinguish permanent (P)- and transient (T)-CH. We retrospectively analyzed the cl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab49492712171be8fa4fe1fec01cf75
http://europepmc.org/articles/PMC7534519

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A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation

Autor: Yusuke Tanahashi, Tokuo Mukai, Osamu Ueda, Kumihiro Matsuo, Yoshiya Ito, Akimasa Okuno, Shigeru Suzuki, Kenji Fujieda, Tsunehisa Nagamori, Akiko Furuya, Hiroshi Azuma, Takahide Kokumai, Koichi Yano

Publikováno v: European journal of medical genetics. 63(11)

Biallelic neuroblastoma ampliﬁed sequence (NBAS) gene mutations have recently been identified to cause a reduction in its protein expression and a broad phenotypic spectrum, from isolated short stature, optic nerve atrophy, and Pelger-Huet anomaly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0cad460ee0832e149a777c3f7faf843
https://pubmed.ncbi.nlm.nih.gov/32805445

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Glycemic control indicator levels at diagnosis of neonatal diabetes mellitus: Comparison with other types of insulin-dependent diabetes mellitus

Autor: Soji Kasayama, Masafumi Koga, Yusuke Tanahashi, Yukihiro Bando, Shigeru Suzuki, Hiroshi Azuma, Akiko Furuya

Publikováno v: Pediatric Diabetes. 18:767-771

Background Neonatal diabetes mellitus (NDM) is a monogenic insulin-dependent diabetes that develops within 6 months of age. The progression of hyperglycemia until diagnosis is unknown. Glycemic control indicators at diagnosis are useful to estimate t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4966e7d4dab650167115d5e42acd3d54
https://doi.org/10.1111/pedi.12481

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Age-Adjusted Glycated Albumin at Diagnosis is more Correlated with the Product of Age and Plasma Glucose than Plasma Glucose Alone in Patients with Neonatal Diabetes Mellitus

Autor: Tatsuhiko Urakami, Hiroshi Azuma, Atsushi Nakao, Katsumi Ushijima, Aya Imamoto, Yusuke Tanahashi, Miho Oshima, Mariko Araki, Shigeru Suzuki, Kumihiro Matsuo, Kayo Mizutani, Nobuhiko Nagano, Satoshi Hayano, Satoshi Amamiya, Masafumi Koga, Akiko Furuya

Publikováno v: Journal of Clinical Laboratory Analysis. 30:1086-1091

Background We previously showed that glycated albumin (GA) is a useful glycemic control indicator in patients with neonatal diabetes mellitus (NDM), and that age-adjusted GA (Aa-GA) can reflect more accurately glycemic control status. Here, we invest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38391314b474d4f141b888ab519cb957
https://doi.org/10.1002/jcla.21985

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