BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 36407031)

  • 1. RET T244I Germline Variant Mutation in a Patient with Pancreatic Paraganglioma and Primary Hyperparathyroidism.
    Kim M; Aploks K; Vargas-Pinto S; Dong X
    Int J Endocrinol Metab; 2022 Jul; 20(3):e121056. PubMed ID: 36407031
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma.
    Korpershoek E; Petri BJ; van Nederveen FH; Dinjens WN; Verhofstad AA; de Herder WW; Schmid S; Perren A; Komminoth P; de Krijger RR
    Endocr Relat Cancer; 2007 Jun; 14(2):453-62. PubMed ID: 17639058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Laparoscopic excision of a familial paraganglioma.
    Kelliher K; Santiago A; Estrada DE; Campbell BT
    J Laparoendosc Adv Surg Tech A; 2009 Apr; 19 Suppl 1():S155-8. PubMed ID: 19260793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.
    Mete O; Asa SL; Gill AJ; Kimura N; de Krijger RR; Tischler A
    Endocr Pathol; 2022 Mar; 33(1):90-114. PubMed ID: 35285002
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression analysis of RET and the GDNF/GFRalpha-1 and NTN/GFRalpha-2 ligand complexes in pheochromocytomas and paragangliomas.
    Edström E; Frisk T; Farnebo F; Höög A; Bäckdahl M; Larsson C
    Int J Mol Med; 2000 Oct; 6(4):469-74. PubMed ID: 10998441
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of the RET proto-oncogene in sporadic hyperparathyroidism and in hyperparathyroidism of multiple endocrine neoplasia type 2.
    Pausova Z; Soliman E; Amizuka N; Janicic N; Konrad EM; Arnold A; Goltzman D; Hendy GN
    J Clin Endocrinol Metab; 1996 Jul; 81(7):2711-8. PubMed ID: 8675600
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Paragangliomas/Pheochromocytomas: clinically oriented genetic testing.
    Martins R; Bugalho MJ
    Int J Endocrinol; 2014; 2014():794187. PubMed ID: 24899893
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Rare Case of Thoracoabdominal Paraganglioma: A Case Report and Literature Review.
    Baptista P; Benido Silva V; Cruz AR; Fonseca L; Palma I
    Cureus; 2022 Dec; 14(12):e32504. PubMed ID: 36654613
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Germline gene testing of the RET, VHL, SDHD and SDHB genes in patients with pheochromocytoma/paraganglioma].
    Wu K; Zhang Y; Zhang H; Tan ZH; Guo XH; Yang JM
    Beijing Da Xue Xue Bao Yi Xue Ban; 2018 Aug; 50(4):634-639. PubMed ID: 30122763
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple endocrine neoplasia type 2.
    Gertner ME; Kebebew E
    Curr Treat Options Oncol; 2004 Aug; 5(4):315-25. PubMed ID: 15233908
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas.
    Krawczyk A; Hasse-Lazar K; Pawlaczek A; Szpak-Ulczok S; Krajewska J; Paliczka-Cieślak E; Jurecka-Lubieniecka B; Roskosz J; Chmielik E; Ziaja J; Cierpka L; Peczkowska M; Preibisz A; Januszewicz A; Otto M; Jarzab B
    Endokrynol Pol; 2010; 61(1):43-8. PubMed ID: 20205103
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors.
    Babic B; Patel D; Aufforth R; Assadipour Y; Sadowski SM; Quezado M; Nilubol N; Prodanov T; Pacak K; Kebebew E
    Surgery; 2017 Jan; 161(1):220-227. PubMed ID: 27865588
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.
    Korpershoek E; Van Nederveen FH; Dannenberg H; Petri BJ; Komminoth P; Perren A; Lenders JW; Verhofstad AA; De Herder WW; De Krijger RR; Dinjens WN
    Ann N Y Acad Sci; 2006 Aug; 1073():138-48. PubMed ID: 17102080
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas.
    Dannenberg H; Komminoth P; Dinjens WN; Speel EJ; de Krijger RR
    Endocr Pathol; 2003; 14(4):329-50. PubMed ID: 14739490
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.
    Neumann HP; Eng C; Mulligan LM; Glavac D; Zäuner I; Ponder BA; Crossey PA; Maher ER; Brauch H
    JAMA; 1995 Oct; 274(14):1149-51. PubMed ID: 7563486
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pheochromocytomas and Paragangliomas: An Update on Recent Molecular Genetic Advances and Criteria for Malignancy.
    Guo Z; Lloyd RV
    Adv Anat Pathol; 2015 Sep; 22(5):283-93. PubMed ID: 26262510
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phaeochromocytoma: a catecholamine and oxidative stress disorder.
    Pacak K
    Endocr Regul; 2011 Apr; 45(2):65-90. PubMed ID: 21615192
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Homozygous RET K666N Genotype With an MEN2A Phenotype.
    Jaber T; Hyde SM; Cote GJ; Grubbs EG; Giles WH; Stevens CA; Dadu R
    J Clin Endocrinol Metab; 2018 Apr; 103(4):1269-1272. PubMed ID: 29408964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetics of pheochromocytoma and the relevance in surgery].
    von Dobschütz E; Neumann HPH
    Chirurg; 2019 Jan; 90(1):15-22. PubMed ID: 30306232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Somatic RET mutation in a patient with pigmented adrenal pheochromocytoma.
    Maison N; Korpershoek E; Eisenhofer G; Robledo M; de Krijger R; Beuschlein F
    Endocrinol Diabetes Metab Case Rep; 2016; 2016():150117. PubMed ID: 26843961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.