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3. 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]
4. 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]
5. 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]
6. 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]
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8. 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]
9. Genetics of primary bilateral macronodular adrenal hyperplasia: a model for early diagnosis of Cushing's syndrome? Drougat L; Espiard S; Bertherat J Eur J Endocrinol; 2015 Oct; 173(4):M121-31. PubMed ID: 26264719 [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]
12. 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]
13. [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]
14. 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]
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20. 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] [Next] [New Search]