BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 37625448)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9.
    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]  

  • 10. ARMC5 Alterations in Patients With Sporadic Neuroendocrine Tumors and Multiple Endocrine Neoplasia Type 1 (MEN1).
    Damjanovic SS; Antic JA; Elezovic-Kovacevic VI; Dundjerovic DM; Milicevic IT; Beleslin-Cokic BB; Ilic BB; Rodic GS; Berthon A; Maria AG; Faucz FR; Stratakis CA
    J Clin Endocrinol Metab; 2020 Dec; 105(12):e4531-42. PubMed ID: 32901291
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. Prevalence and phenotype of primary bilateral macronodular adrenal hyperplasia with autonomous cortisol secretion: a study of 98 patients.
    Bengoa-Rojano N; Fernández-Argüeso M; Botella-Carretero JI; Pascual-Corrales E; Araujo-Castro M
    Rev Clin Esp (Barc); 2022 Oct; 222(8):458-467. PubMed ID: 35597729
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Macronodular adrenal hyperplasia causing Cushing's syndrome due to ARMC5 gene mutation.].
    Hella Z; Tőke J; Patócs A; Varga Z; Dabasi G; Kovács GL; Tóth M
    Orv Hetil; 2023 Aug; 164(32):1271-1277. PubMed ID: 37573559
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The degree of cortisol secretion is associated with diabetes mellitus and hypertension in patients with nonfunctioning adrenal tumors.
    Favero V; Aresta C; Parazzoli C; Cairoli E; Eller-Vainicher C; Palmieri S; Salcuni AS; Arosio M; Persani L; Scillitani A; Morelli V; Chiodini I
    Cardiovasc Diabetol; 2023 May; 22(1):102. PubMed ID: 37131218
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Clinical, Pathophysiologic, Genetic, and Therapeutic Progress in Primary Bilateral Macronodular Adrenal Hyperplasia.
    Bertherat J; Bourdeau I; Bouys L; Chasseloup F; Kamenický P; Lacroix A
    Endocr Rev; 2023 Jul; 44(4):567-628. PubMed ID: 36548967
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Pituitary Macroadenoma With Macronodular Adrenal Hyperplasia and Novel Armadillo Repeat-Containing Protein 5 (ARMC5) Mutation.
    Khosla S; Alsarraf F; Nylen ES
    JCEM Case Rep; 2024 Feb; 2(2):luad138. PubMed ID: 38222860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.