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6. 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]
7. 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]
8. 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]
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. 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]
16. 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]
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]
18. 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]
19. Do patients with incidentally discovered bilateral adrenal nodules represent an early form of ARMC5-mediated bilateral macronodular hyperplasia? Emms H; Tsirou I; Cranston T; Tsagarakis S; Grossman AB Endocrine; 2016 Sep; 53(3):801-8. PubMed ID: 27306888 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]