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.
160 related articles for article (PubMed ID: 32713866)
1. 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]
2. Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma. Elbelt U; Trovato A; Kloth M; Gentz E; Finke R; Spranger J; Galas D; Weber S; Wolf C; König K; Arlt W; Büttner R; May P; Allolio B; Schneider JG J Clin Endocrinol Metab; 2015 Jan; 100(1):E119-28. PubMed ID: 25279498 [TBL] [Abstract][Full Text] [Related]
6. A Novel Eghbali M; Cheraghi S; Samanian S; Rad I; Meghdadi J; Akbari H; Honardoost M Diagnostics (Basel); 2022 Dec; 12(12):. PubMed ID: 36553033 [TBL] [Abstract][Full Text] [Related]
7. Whole-genome sequencing revealed armadillo repeat containing 5 (ARMC5) mutation in a Chinese family with ACTH-independent macronodular adrenal hyperplasia. Zhang Q; Cui L; Gao JP; Yan WH; Jin N; Chen K; Zang L; Du J; Wang XL; Guo QH; Yang GQ; Yang LJ; Ba JM; Gu WJ; Lv ZH; Dou JT; Mu YM; Lu JM Endocr J; 2018 Mar; 65(3):269-279. PubMed ID: 29279458 [TBL] [Abstract][Full Text] [Related]
8. A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report. Liu Q; Tong D; Xu J; Yang X; Yi Y; Zhang D; Wang L; Zhang J; Zhang Y; Li Y; Chang L; Chen R; Guan Y; Yi X; Jiang J BMC Med Genet; 2018 Mar; 19(1):49. PubMed ID: 29587644 [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. The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia. Correa R; Zilbermint M; Berthon A; Espiard S; Batsis M; Papadakis GZ; Xekouki P; Lodish MB; Bertherat J; Faucz FR; Stratakis CA Eur J Endocrinol; 2015 Oct; 173(4):435-40. PubMed ID: 26162405 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. ARMC5 mutations in a large French-Canadian family with cortisol-secreting β-adrenergic/vasopressin responsive bilateral macronodular adrenal hyperplasia. Bourdeau I; Oble S; Magne F; Lévesque I; Cáceres-Gorriti KY; Nolet S; Awadalla P; Tremblay J; Hamet P; Fragoso MC; Lacroix A Eur J Endocrinol; 2016 Jan; 174(1):85-96. PubMed ID: 26604299 [TBL] [Abstract][Full Text] [Related]