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23. 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]
24. [Bilateral massive macronodular adrenal gland hyperplasia. A rare cause of Cushing's syndrome]. Strohm M; Reincke M; Theiss M; Diehl KL; Allolio B Dtsch Med Wochenschr; 1994 Feb; 119(6):180-4. PubMed ID: 8306853 [TBL] [Abstract][Full Text] [Related]
25. 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]
27. Clinicopathological correlates of adrenal Cushing's syndrome. Duan K; Gomez Hernandez K; Mete O J Clin Pathol; 2015 Mar; 68(3):175-86. PubMed ID: 25425660 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Severe osteoporosis in a young man with bilateral Cushing's syndrome: a case report. Reis BO; Leal CTS; Ezequiel DGA; Dos Santos Ribeiro Simões Juliano AC; de Macedo Veloso FL; da Silva LM; Ferreira LV; Ferreira M; De Oliveira Souza GZ J Med Case Rep; 2023 Jun; 17(1):251. PubMed ID: 37328870 [TBL] [Abstract][Full Text] [Related]
30. [Cushing's syndrome due to bilateral adrenal macronodular hyperplasia. From ACTH-dependent hypercortisolism to ACTH-independent hypercortisolism]. López JM; Sapunar J; Donoso J; Martínez P Rev Med Chil; 1991 Oct; 119(10):1165-70. PubMed ID: 1668993 [TBL] [Abstract][Full Text] [Related]
31. A case of severe hypertension caused by ACTH-independent macronodular adrenal hyperplasia. Nocente R; De ML; Mancini A; Bianchi A; Bellantone R; Lauriola L; Costanzo M; De CC; Gasbarrini G; Gentiloni SN J Endocrinol Invest; 2002 Mar; 25(3):254-8. PubMed ID: 11936469 [TBL] [Abstract][Full Text] [Related]
36. A case of adrenocorticotropin-independent bilateral adrenal macronodular hyperplasia (AIMAH) with primary hyperparathyroidism (PHPT). Sato M; Soma M; Nakayama T; Kosuge K; Suzuki R; Okada K; Komatsu K; Sugitani M; Matsumoto K Endocr J; 2006 Feb; 53(1):111-7. PubMed ID: 16543680 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]