Zobrazeno 1 - 10
of 916
pro vyhledávání: '"MODY 5"'
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism. Feb2024, Vol. 29 Issue 1, p70-72. 3p.
Autor:
Lee J; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea., Kim M; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea., Yoo S; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea., Yoon JY; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea., Cheon CK; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea.
Publikováno v:
Annals of pediatric endocrinology & metabolism [Ann Pediatr Endocrinol Metab] 2024 Feb; Vol. 29 (1), pp. 70-72. Date of Electronic Publication: 2024 Feb 29.
Autor:
Veerareddy S; Mediciti Institute of Medical Sciences, Telangana, India., Reddy S; University of North Carolina School of Medicine, Chapel Hill, NC., Barreto M; Childrens National Hospital, Washington, DC., Vedherey N; West Virginia School of Osteopathic Medicine, Lewisburg, WV., Gopalareddy VV; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Levine Childrens Hospital at Atrium Health, Charlotte, NC.
Publikováno v:
ACG case reports journal [ACG Case Rep J] 2023 Oct 03; Vol. 10 (10), pp. e01150. Date of Electronic Publication: 2023 Oct 03 (Print Publication: 2023).
Akademický článek
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Maturity-onset diabetes of the young type 5 (MODY5) is a rare subtype of MODYs. It caused by mutations of the hepatocyte nuclear factor 1 homeobox b gene (HNF1B). A 21-year-old young woman was admitted to our hospital for severe malnutrition and gast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be0e4f6fb33ad5d358b3f3e7bf60d707
https://doi.org/10.21203/rs.3.rs-964266/v1
https://doi.org/10.21203/rs.3.rs-964266/v1
Autor:
Almeida, Nestor
Publikováno v:
In Kidney International Reports April 2024 9(4) Supplement:S347-S348
Autor:
Kunimasa Yagi, Kazuyuki Tobe, Jianhui Liu, Yukio Horikawa, Takahide Kuwano, Ayumi Nishimura, Hisae Honoki, Daisuke Chujo, Asako Enkaku, Shiho Fujisaka, Akiko Takikawa, Yoshiyuki Watanabe, Minoru Iwata, Yoshiyuki Omura, Mayumi Enya
Publikováno v:
Endocrine Journal. 66:1113-1116
We report a sporadic case of maturity-onset diabetes of the young type 5 (MODY5) with a whole-gene deletion of the hepatocyte nuclear factor-1beta (HNF1B) gene. A 44-year-old Japanese man who had been diagnosed with early-onset non-autoimmune diabete
Publikováno v:
Diabetes. 70
Objective: Mutations in hepatocyte nuclear factor 1B (HNF1B), are often identified based on a history of renal disease and diabetes mellitus, but other endocrine manifestations including dyslipidemia and hyperparathyroidism have not been well-defined
Publikováno v:
Endocrine Abstracts.
Akademický článek
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