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5. 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]
6. 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]
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]
9. 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]
10. 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]
11. 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]
13. ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia. Gagliardi L; Schreiber AW; Hahn CN; Feng J; Cranston T; Boon H; Hotu C; Oftedal BE; Cutfield R; Adelson DL; Braund WJ; Gordon RD; Rees DA; Grossman AB; Torpy DJ; Scott HS J Clin Endocrinol Metab; 2014 Sep; 99(9):E1784-92. PubMed ID: 24905064 [TBL] [Abstract][Full Text] [Related]
14. Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation. Faucz FR; Zilbermint M; Lodish MB; Szarek E; Trivellin G; Sinaii N; Berthon A; Libé R; Assié G; Espiard S; Drougat L; Ragazzon B; Bertherat J; Stratakis CA J Clin Endocrinol Metab; 2014 Jun; 99(6):E1113-9. PubMed ID: 24601692 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. Familial bilateral macronodular adrenal hyperplasia due to a novel ARMC 5 germline mutation: Clinical status and possible association with other neoplasms. Piñar-Gutiérrez A; Mangas-Cruz MÁ; de Lara-Rodríguez I; Remón-Ruiz P; Del Can-Sánchez D; Tous Castillo M; Pumar-López A Endocrinol Diabetes Nutr (Engl Ed); 2024 Mar; 71(3):119-123. PubMed ID: 38555108 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
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]