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Journal Abstract Search

423 related items for PubMed ID: 17102080

  • 1. 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
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  • 4. Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
    Pandit R, Khadilkar K, Sarathi V, Kasaliwal R, Goroshi M, Khare S, Nair S, Raghavan V, Dalvi A, Hira P, Fernandes G, Sathe P, Rojekar A, Malhotra G, Bakshi G, Prakash G, Bhansali A, Walia R, Kamalanathan S, Sahoo J, Desai A, Bhagwat N, Mappa P, Rajput R, Chandrashekhar SR, Shivane V, Menon P, Lila A, Bandgar T, Shah N.
    Eur J Endocrinol; 2016 Oct; 175(4):311-23. PubMed ID: 27539324
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  • 5. Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.
    Meyer-Rochow GY, Smith JM, Richardson AL, Marsh DJ, Sidhu SB, Robinson BG, Benn DE.
    J Surg Res; 2009 Nov; 157(1):55-62. PubMed ID: 19215943
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  • 9. Genetic testing in pheochromocytoma or functional paraganglioma.
    Amar L, Bertherat J, Baudin E, Ajzenberg C, Bressac-de Paillerets B, Chabre O, Chamontin B, Delemer B, Giraud S, Murat A, Niccoli-Sire P, Richard S, Rohmer V, Sadoul JL, Strompf L, Schlumberger M, Bertagna X, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP.
    J Clin Oncol; 2005 Dec 01; 23(34):8812-8. PubMed ID: 16314641
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  • 13. Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes.
    Gill AJ, Benn DE, Chou A, Clarkson A, Muljono A, Meyer-Rochow GY, Richardson AL, Sidhu SB, Robinson BG, Clifton-Bligh RJ.
    Hum Pathol; 2010 Jun 01; 41(6):805-14. PubMed ID: 20236688
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  • 16. Mutation screening in a Norwegian cohort with pheochromocytoma.
    Sjursen W, Halvorsen H, Hofsli E, Bachke S, Berge A, Engebretsen LF, Falkmer SE, Falkmer UG, Varhaug JE.
    Fam Cancer; 2013 Sep 01; 12(3):529-35. PubMed ID: 23407919
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  • 17. Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?
    Jiménez C, Cote G, Arnold A, Gagel RF.
    J Clin Endocrinol Metab; 2006 Aug 01; 91(8):2851-8. PubMed ID: 16735498
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  • 18. Is genetic screening indicated in apparently sporadic pheochromocytomas and paragangliomas?
    Iacobone M, Schiavi F, Bottussi M, Taschin E, Bobisse S, Fassina A, Opocher G, Favia G.
    Surgery; 2011 Dec 01; 150(6):1194-201. PubMed ID: 22136840
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  • 19. Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.
    Mora J, Cascón A, Robledo M, Catala A.
    Pediatr Blood Cancer; 2006 Nov 01; 47(6):785-9. PubMed ID: 16304664
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  • 20. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
    Benn DE, Croxson MS, Tucker K, Bambach CP, Richardson AL, Delbridge L, Pullan PT, Hammond J, Marsh DJ, Robinson BG.
    Oncogene; 2003 Mar 06; 22(9):1358-64. PubMed ID: 12618761
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