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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 24905064)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. ARMC5 mutations are a frequent cause of primary macronodular adrenal Hyperplasia.
    Alencar GA; Lerario AM; Nishi MY; Mariani BM; Almeida MQ; Tremblay J; Hamet P; Bourdeau I; Zerbini MC; Pereira MA; Gomes GC; Rocha Mde S; Chambo JL; Lacroix A; Mendonca BB; Fragoso MC
    J Clin Endocrinol Metab; 2014 Aug; 99(8):E1501-9. PubMed ID: 24708098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 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]  

  • 11. 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]  

  • 12. GERMLINE DELETION OF ARMC5 IN FAMILIAL PRIMARY MACRONODULAR ADRENAL HYPERPLASIA.
    Suzuki S; Tatsuno I; Oohara E; Nakayama A; Komai E; Shiga A; Kono T; Takiguchi T; Higuchi S; Sakuma I; Nagano H; Hashimoto N; Mayama T; Koide H; Sasano H; Nakatani Y; Imamoto T; Ichikawa T; Yokote K; Tanaka T
    Endocr Pract; 2015 Oct; 21(10):1152-60. PubMed ID: 26214113
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome.
    Assié G; Libé R; Espiard S; Rizk-Rabin M; Guimier A; Luscap W; Barreau O; Lefèvre L; Sibony M; Guignat L; Rodriguez S; Perlemoine K; René-Corail F; Letourneur F; Trabulsi B; Poussier A; Chabbert-Buffet N; Borson-Chazot F; Groussin L; Bertagna X; Stratakis CA; Ragazzon B; Bertherat J
    N Engl J Med; 2013 Nov; 369(22):2105-14. PubMed ID: 24283224
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allelic Variants of
    Mariani BMP; Nishi MY; Wanichi IQ; Brondani VB; Lacombe AMF; Charchar H; Pereira MAA; Srougi V; Tanno FY; Ceccato F; Regazzo D; Barbot M; Occhi G; Albiger NME; Vieira-Corrêa M; Kater CE; Scaroni C; Chambô JL; Zerbini MCN; Mendonca BB; Almeida MQ; Fragoso MCBV
    Front Endocrinol (Lausanne); 2020; 11():36. PubMed ID: 32117062
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Genetic basis of bilateral macronodular hyperplasia.
    Ravikumar A; Levine AC
    Endocr Pract; 2015 Apr; 21(4):390-4. PubMed ID: 25536975
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences.
    Espiard S; Drougat L; Libé R; Assié G; Perlemoine K; Guignat L; Barrande G; Brucker-Davis F; Doullay F; Lopez S; Sonnet E; Torremocha F; Pinsard D; Chabbert-Buffet N; Raffin-Sanson ML; Groussin L; Borson-Chazot F; Coste J; Bertagna X; Stratakis CA; Beuschlein F; Ragazzon B; Bertherat J
    J Clin Endocrinol Metab; 2015 Jun; 100(6):E926-35. PubMed ID: 25853793
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions.
    Mulatero P; Schiavi F; Williams TA; Monticone S; Barbon G; Opocher G; Fallo F
    J Hum Hypertens; 2016 Jun; 30(6):374-8. PubMed ID: 26446392
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.