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Journal Abstract Search

161 related items for PubMed ID: 23407919

  • 1. 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; 12(3):529-35. PubMed ID: 23407919
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden.
    Muth A, Abel F, Jansson S, Nilsson O, Ahlman H, Wängberg B.
    World J Surg; 2012 Jun; 36(6):1389-94. PubMed ID: 22270996
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  • 6. Mutations and polymorphisms in the SDHB, SDHD, VHL, and RET genes in sporadic and familial pheochromocytomas.
    Waldmann J, Langer P, Habbe N, Fendrich V, Ramaswamy A, Rothmund M, Bartsch DK, Slater EP.
    Endocrine; 2009 Jun; 35(3):347-55. PubMed ID: 19399650
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.
    Castellano M, Mori L, Giacchè M, Agliozzo E, Tosini R, Panarotto A, Cappelli C, Mulatero P, Cumetti D, Veglio F, Agabiti-Rosei E.
    Ann N Y Acad Sci; 2006 Aug; 1073():156-65. PubMed ID: 17102082
    [Abstract] [Full Text] [Related]

  • 9. 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 Aug; 61(1):43-8. PubMed ID: 20205103
    [Abstract] [Full Text] [Related]

  • 10. Semiquantitative 123I-Metaiodobenzylguanidine Scintigraphy to Distinguish Pheochromocytoma and Paraganglioma from Physiologic Adrenal Uptake and Its Correlation with Genotype-Dependent Expression of Catecholamine Transporters.
    van Berkel A, Rao JU, Lenders JW, Pellegata NS, Kusters B, Piscaer I, Hermus AR, Plantinga TS, Langenhuijsen JF, Vriens D, Janssen MJ, Gotthardt M, Timmers HJ.
    J Nucl Med; 2015 Jun; 56(6):839-46. PubMed ID: 25883126
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Risk-oriented approach to hereditary adrenal pheochromocytoma.
    Machens A, Brauckhoff M, Gimm O, Dralle H.
    Ann N Y Acad Sci; 2006 Aug 01; 1073():417-28. PubMed ID: 17102110
    [Abstract] [Full Text] [Related]

  • 13. Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.
    Fishbein L, Merrill S, Fraker DL, Cohen DL, Nathanson KL.
    Ann Surg Oncol; 2013 May 01; 20(5):1444-50. PubMed ID: 23512077
    [Abstract] [Full Text] [Related]

  • 14. Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.
    Weber A, Hoffmann MM, Neumann HP, Erlic Z.
    Horm Cancer; 2012 Aug 01; 3(4):187-92. PubMed ID: 22573489
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  • 16. [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 18; 50(4):634-639. PubMed ID: 30122763
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  • 19. 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 18; 41(6):805-14. PubMed ID: 20236688
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