These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 36727580)
1. New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH). Giacché M; Panarotto A; Mori L; Poliani PL; Lanzi R; Lena MS; Castellano M Mol Genet Genomic Med; 2023 Apr; 11(4):e2126. PubMed ID: 36727580 [TBL] [Abstract][Full Text] [Related]
2. A novel pathogenic variant of ARMC5 in a patient with primary bilateral macronodular adrenal hyperplasia: a case report. Wang W; Wei F BMC Endocr Disord; 2022 Aug; 22(1):211. PubMed ID: 35996143 [TBL] [Abstract][Full Text] [Related]
3. Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) patient with ARMC5 mutations. Tang P; Zhang J; Peng S; Yan X; Wang Y; Wang S; Zhang Y; Liu G; Xu J; Huang Y; Zhang D; Liu Q; Jiang J; Lan W BMC Endocr Disord; 2023 Apr; 23(1):77. PubMed ID: 37029354 [TBL] [Abstract][Full Text] [Related]
4. High expression of adrenal P450 aromatase (CYP19A1) in association with ARMC5-primary bilateral macronodular adrenocortical hyperplasia. Berthon A; Hannah-Shmouni F; Maria AG; Faucz FR; Stratakis CA J Steroid Biochem Mol Biol; 2019 Jul; 191():105316. PubMed ID: 31014964 [TBL] [Abstract][Full Text] [Related]
5. ARMC5 mutations in familial and sporadic primary bilateral macronodular adrenal hyperplasia. Yu L; Zhang J; Guo X; Chen X; He Z; He Q PLoS One; 2018; 13(1):e0191602. PubMed ID: 29370219 [TBL] [Abstract][Full Text] [Related]
7. Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia: a case report. Jojima T; Kogai T; Iijima T; Kato K; Sagara M; Kezuka A; Kase M; Sakurai S; Akimoto K; Sakumoto J; Namatame T; Ueki K; Hishinuma A; Kamai T; Usui I; Aso Y Eur J Endocrinol; 2020 Dec; 183(6):K7-K12. PubMed ID: 33105102 [TBL] [Abstract][Full Text] [Related]
8. A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype. Albiger NM; Regazzo D; Rubin B; Ferrara AM; Rizzati S; Taschin E; Ceccato F; Arnaldi G; Pecori Giraldi F; Stigliano A; Cerquetti L; Grimaldi F; De Menis E; Boscaro M; Iacobone M; Occhi G; Scaroni C Endocrine; 2017 Mar; 55(3):959-968. PubMed ID: 27094308 [TBL] [Abstract][Full Text] [Related]
9. Extensive ARMC5 genetic variance in primary bilateral macronodular adrenal hyperplasia that started with exophthalmos: a case report. Jin P; Janjua MU; Zhang Q; Dong CS; Yang Y; Mo ZH J Med Case Rep; 2018 Jan; 12(1):13. PubMed ID: 29343284 [TBL] [Abstract][Full Text] [Related]
10. A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia. He WT; Wang X; Song W; Song XD; Lu YJ; Lv YK; He T; Yu XF; Hu SH BMC Med Genomics; 2021 May; 14(1):126. PubMed ID: 33971873 [TBL] [Abstract][Full Text] [Related]
16. [Hereditary Cushing's syndrome caused by primary bilateral macronodular adrenal hyperplasia due to ARMC5 mutation with concomitant primary hyperparathyroidism: the first known case in Russia]. Mamedova EO; Vasilyev EV; Petrov VM; Izmailova NS; Buryakina SA; Rozhinskaya LY; Tiulpakov AN; Belaya ZE Probl Endokrinol (Mosk); 2019 Jun; 65(2):89-94. PubMed ID: 31271710 [TBL] [Abstract][Full Text] [Related]
17. Primary macronodular adrenal hyperplasia (PMAH) can be generated by a new ARMC5 germline variant (c.52C>T (p.Gln18X)). Zhang F; Lin X; Yu X Endocr J; 2020 Dec; 67(12):1179-1186. PubMed ID: 32713866 [TBL] [Abstract][Full Text] [Related]