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late-onset isolated ACTH deficiency 相关文献:
Late-Onset Isolated Corticotrope Deficiency in a Woman with Down Syndrome.
Oueslati I, Ben Jemaa M, Yazidi M, Chaker F, Chihaoui M.
Case Rep Endocrinol. 2021 Apr 27;2021:5562831. doi: 10.1155/2021/5562831. eCollection 2021.
PMID:34007493
Late-onset isolated adrenocorticotropic hormone deficiency caused by nivolumab: a case report.
Takeno A, Yamamoto M, Morita M, Tanaka S, Kanazawa I, Yamauchi M, Kaneko S, Sugimoto T.
BMC Endocr Disord. 2019 Feb 19;19(1):25. doi: 10.1186/s12902-019-0335-x.
PMID:30782163
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency.
Metherell LA, Savage MO, Dattani M, Walker J, Clayton PE, Farooqi IS, Clark AJ.
Eur J Endocrinol. 2004 Oct;151(4):463-5. doi: 10.1530/eje.0.1510463.
PMID:15476446
Clinical, biological and genetic analysis of 8 cases of congenital isolated adrenocorticotrophic hormone (ACTH) deficiency.
Pham LL, Garot C, Brue T, Brauner R.
PLoS One. 2011;6(10):e26516. doi: 10.1371/journal.pone.0026516. Epub 2011 Oct 18.
PMID:22028893
Growth hormone deficiency with late-onset hypothalamic hypoadrenocorticism associated with respiratory and renal dysfunction: a case report.
Kojima N, Koriyama N, Tokito A, Ogiso K, Kusumoto K, Kubo S, Nishio Y.
BMC Endocr Disord. 2020 Apr 16;20(1):50. doi: 10.1186/s12902-020-0536-3.
PMID:32299407
Two Cases of Atezolizumab-Induced Hypophysitis.
Kanie K, Iguchi G, Bando H, Fujita Y, Odake Y, Yoshida K, Matsumoto R, Fukuoka H, Ogawa W, Takahashi Y.
J Endocr Soc. 2017 Dec 13;2(1):91-95. doi: 10.1210/js.2017-00414. eCollection 2018 Jan 1.
PMID:29362727
Isolated ACTH deficiency in self referred patients for LOH syndrome: two case reports.
Sato Y, Tanda H, Nakajima H, Nitta T, Akagashi K, Hanzawa T, Tobe M, Haga K, Uchida K, Honma I.
Reprod Med Biol. 2012 Feb 26;11(3):155-158. doi: 10.1007/s12522-012-0121-1. eCollection 2012 Jul.
PMID:29662363
Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid deficiency type 2.
Hughes CR, Chung TT, Habeb AM, Kelestimur F, Clark AJ, Metherell LA.
J Clin Endocrinol Metab. 2010 Jul;95(7):3497-501. doi: 10.1210/jc.2009-2731. Epub 2010 Apr 28.
PMID:20427498
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations.
Couture C, Saveanu A, Barlier A, Carel JC, Fassnacht M, Flück CE, Houang M, Maes M, Phan-Hug F, Enjalbert A, Drouin J, Brue T, Vallette S.
J Clin Endocrinol Metab. 2012 Mar;97(3):E486-95. doi: 10.1210/jc.2011-1659. Epub 2011 Dec 14.
PMID:22170728
Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency.
Dewailly D, Vantyghem-Haudiquet MC, Sainsard C, Buvat J, Cappoen JP, Ardaens K, Racadot A, Lefebvre J, Fossati P.
J Clin Endocrinol Metab. 1986 Aug;63(2):418-23. doi: 10.1210/jcem-63-2-418.
PMID:3013919
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