BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 28870973)

  • 1. Primary hyperparathyroidism in young patients in Russia: high frequency of hyperparathyroidism-jaw tumor syndrome.
    Mamedova E; Mokrysheva N; Vasilyev E; Petrov V; Pigarova E; Kuznetsov S; Kuznetsov N; Rozhinskaya L; Melnichenko G; Dedov I; Tiulpakov A
    Endocr Connect; 2017 Nov; 6(8):557-565. PubMed ID: 28870973
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Germline Mutations Related to Primary Hyperparathyroidism Identified by Next-Generation Sequencing.
    Park HS; Lee YH; Hong N; Won D; Rhee Y
    Front Endocrinol (Lausanne); 2022; 13():853171. PubMed ID: 35586626
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study.
    Song A; Yang Y; Jiang Y; Nie M; Jiang Y; Li M; Xia W; Xing X; Wang O
    J Bone Miner Res; 2023 Sep; 38(9):1322-1333. PubMed ID: 37449924
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics of parathyroid tumours.
    Thakker RV
    J Intern Med; 2016 Dec; 280(6):574-583. PubMed ID: 27306766
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated Hypercalcemia.
    Khairi S; Osborne J; Jacobs MF; Clines GT; Miller BS; Hughes DT; Else T
    Horm Cancer; 2020 Oct; 11(5-6):250-255. PubMed ID: 32761341
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism.
    van der Tuin K; Tops CMJ; Adank MA; Cobben JM; Hamdy NAT; Jongmans MC; Menko FH; van Nesselrooij BPM; Netea-Maier RT; Oosterwijk JC; Valk GD; Wolffenbuttel BHR; Hes FJ; Morreau H
    J Clin Endocrinol Metab; 2017 Dec; 102(12):4534-4540. PubMed ID: 29040582
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular pathogenesis of primary hyperparathyroidism.
    Cetani F; Pardi E; Borsari S; Marcocci C
    J Endocrinol Invest; 2011 Jul; 34(7 Suppl):35-9. PubMed ID: 21985978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation.
    Shibata Y; Yamazaki M; Takei M; Uchino S; Sakurai A; Komatsu M
    Endocr J; 2015; 62(7):627-32. PubMed ID: 25959515
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort.
    Mariathasan S; Andrews KA; Thompson E; Challis BG; Wilcox S; Pierce H; Hale J; Spiden S; Fuller G; Simpson HL; Fish B; Jani P; Seetho I; Armstrong R; Izatt L; Joshi M; Velusamy A; Park SM; Casey RT
    Clin Endocrinol (Oxf); 2020 Oct; 93(4):409-418. PubMed ID: 32430905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequent germ-line mutations of the MEN1, CASR, and HRPT2/CDC73 genes in young patients with clinically non-familial primary hyperparathyroidism.
    Starker LF; Akerström T; Long WD; Delgado-Verdugo A; Donovan P; Udelsman R; Lifton RP; Carling T
    Horm Cancer; 2012 Apr; 3(1-2):44-51. PubMed ID: 22187299
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition.
    Vierimaa O; Villablanca A; Alimov A; Georgitsi M; Raitila A; Vahteristo P; Larsson C; Ruokonen A; Eloranta E; Ebeling TM; Ignatius J; Aaltonen LA; Leisti J; Salmela PI
    J Endocrinol Invest; 2009 Jun; 32(6):512-8. PubMed ID: 19474519
    [TBL] [Abstract][Full Text] [Related]  

  • 12. OVARIAN GRANULOSA CELL TUMOR IN A PATIENT WITH A PATHOGENIC VARIANT IN THE
    Sirbiladze RL; Uyar D; Geurts JL; Shaker JL
    AACE Clin Case Rep; 2019; 5(3):e222-e225. PubMed ID: 31967039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.
    Pardi E; Borsari S; Saponaro F; Bogazzi F; Urbani C; Mariotti S; Pigliaru F; Satta C; Pani F; Materazzi G; Miccoli P; Grantaliano L; Marcocci C; Cetani F
    PLoS One; 2017; 12(10):e0186485. PubMed ID: 29036195
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary Hyperparathyroidism Focused on Molecular Pathogenesis.
    Gómez Sáez JM
    Eur Endocrinol; 2014 Aug; 10(2):153-156. PubMed ID: 29872481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort.
    Mazarico-Altisent I; Capel I; Baena N; Bella-Cueto MR; Barcons S; Guirao X; Pareja R; Muntean A; Arsentales V; Caixàs A; Rigla M
    Front Endocrinol (Lausanne); 2023; 14():1244361. PubMed ID: 37810884
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A family case report of parathyroid carcinoma associated with
    Gu Y; Ye Y; Shu H; Chang L; Xie Y; Li F; Zhu T; Liu M; He Q
    Front Endocrinol (Lausanne); 2024; 15():1330185. PubMed ID: 38348418
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype-Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism.
    Sharma A; Memon S; Lila AR; Sarathi V; Arya S; Jadhav SS; Hira P; Garale M; Gosavi V; Karlekar M; Patil V; Bandgar T
    Calcif Tissue Int; 2022 Sep; 111(3):229-241. PubMed ID: 35567607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple Endocrine Neoplasia Type 1 (MEN1) Phenocopy Due to a Cell Cycle Division 73 (
    Lines KE; Nachtigall LB; Dichtel LE; Cranston T; Boon H; Zhang X; Kooblall KG; Stevenson M; Thakker RV
    J Endocr Soc; 2020 Nov; 4(11):bvaa142. PubMed ID: 33150274
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic defects associated with familial and sporadic hyperparathyroidism.
    Hendy GN; Cole DE
    Front Horm Res; 2013; 41():149-65. PubMed ID: 23652676
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism.
    Alvelos MI; Vinagre J; Fonseca E; Barbosa E; Teixeira-Gomes J; Sobrinho-Simões M; Soares P
    Eur J Endocrinol; 2013 Feb; 168(2):119-28. PubMed ID: 23093699
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.