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 *

197 related articles for article (PubMed ID: 26446392)

  • 21. 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]  

  • 22. Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients.
    Bouys L; Vaczlavik A; Jouinot A; Vaduva P; Espiard S; Assié G; Libé R; Perlemoine K; Ragazzon B; Guignat L; Groussin L; Bricaire L; Cavalcante IP; Bonnet-Serrano F; Lefebvre H; Raffin-Sanson ML; Chevalier N; Touraine P; Jublanc C; Vatier C; Raverot G; Haissaguerre M; Maione L; Kroiss M; Fassnacht M; Christin-Maitre S; Pasmant E; Borson-Chazot F; Tabarin A; Vantyghem MC; Reincke M; Kamenicky P; North MO; Bertherat J
    Eur J Endocrinol; 2022 May; 187(1):123-134. PubMed ID: 35521700
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. Prevalence and clinical features of armadillo repeat-containing 5 mutations carriers in a single center cohort of patients with bilateral adrenal incidentalomas.
    Morelli V; Elli FM; Frigerio S; Vena W; Palmieri S; Lucca C; Maffini MA; Contarino A; Bagnaresi F; Mantovani G; Arosio M
    Eur J Endocrinol; 2023 Aug; 189(2):242-251. PubMed ID: 37625448
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. Molecular mechanisms of
    Stratakis CA; Berthon A
    Curr Opin Endocr Metab Res; 2019 Oct; 8():104-111. PubMed ID: 32864505
    [TBL] [Abstract][Full Text] [Related]  

  • 31. High expression of adrenal P450 aromatase (CYP19A1) in association with ARMC5-primary bilateral macronodular adrenocortical hyperplasia.
    Berthon A; Hannah-Shmouni F; Maria AG; Faucz FR; Stratakis CA
    J Steroid Biochem Mol Biol; 2019 Jul; 191():105316. PubMed ID: 31014964
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Update on primary bilateral macronodular adrenal hyperplasia (PBMAH).
    Bouys L; Chiodini I; Arlt W; Reincke M; Bertherat J
    Endocrine; 2021 Mar; 71(3):595-603. PubMed ID: 33587256
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasia.
    Lao L; Bourdeau I; Gagliardi L; He X; Shi W; Hao B; Tan M; Hu Y; Peng J; Coulombe B; Torpy DJ; Scott HS; Lacroix A; Luo H; Wu J
    Nucleic Acids Res; 2022 Jun; 50(11):6343-6367. PubMed ID: 35687106
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Morphological Harbingers of ARMC5-Pathogenic Variant-Related Bilateral Macronodular Adrenocortical Disease.
    de Arruda Botelho MLA; Nishi MY; Ribeiro KB; Zerbini MCN
    Endocr Pathol; 2023 Jun; 34(2):200-212. PubMed ID: 37043100
    [TBL] [Abstract][Full Text] [Related]  

  • 36.
    Rego T; Fonseca F; Espiard S; Perlemoine K; Bertherat J; Agapito A
    Endocrinol Diabetes Metab Case Rep; 2017; 2017():. PubMed ID: 28458897
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Somatic and inherited mutations in primary aldosteronism.
    Fernandes-Rosa FL; Boulkroun S; Zennaro MC
    J Mol Endocrinol; 2017 Jul; 59(1):R47-R63. PubMed ID: 28400483
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Case Report: A Novel ARMC5 Germline Mutation in a Patient with Primary Bilateral Macronodular Adrenal Hyperplasia and Hypogammaglobulinemia.
    Vena W; Morelli V; Carrabba M; Elli F; Fabio G; Muller I; Lucca C; Maffini MA; Lania AG; Mantovani G; Arosio M
    Front Genet; 2022; 13():834067. PubMed ID: 35368666
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure, and Glycemia in African Americans.
    Joseph JJ; Zhou X; Zilbermint M; Stratakis CA; Faucz FR; Lodish MB; Berthon A; Wilson JG; Hsueh WA; Golden SH; Lin S
    J Clin Endocrinol Metab; 2020 Aug; 105(8):2625-33. PubMed ID: 32436940
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.