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Journal Abstract Search

763 related items for PubMed ID: 12000816

  • 1. Germ-line mutations in nonsyndromic pheochromocytoma.
    Neumann HP, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith WM, Munk R, Manz T, Glaesker S, Apel TW, Treier M, Reineke M, Walz MK, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier-Woelfle M, Peçzkowska M, Szmigielski C, Eng C, Freiburg-Warsaw-Columbus Pheochromocytoma Study Group.
    N Engl J Med; 2002 May 09; 346(19):1459-66. PubMed ID: 12000816
    [Abstract] [Full Text] [Related]

  • 2. 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 11; 274(14):1149-51. PubMed ID: 7563486
    [Abstract] [Full Text] [Related]

  • 3. Pheochromocytoma--death of an axiom.
    Dluhy RG.
    N Engl J Med; 2002 May 09; 346(19):1486-8. PubMed ID: 12000821
    [No Abstract] [Full Text] [Related]

  • 4. [Genetic tests in oncology practice with emphasis on the RET oncogene and VHL tumor suppressor gene].
    Nesković G, Stanojević B, Palmar I, Dimitrijević B.
    Srp Arh Celok Lek; 2002 Jul 09; 130 Suppl 2():52-7. PubMed ID: 12584999
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.
    Opocher G, Conton P, Schiavi F, Macino B, Mantero F.
    Fam Cancer; 2005 Mar 06; 4(1):13-6. PubMed ID: 15883705
    [Abstract] [Full Text] [Related]

  • 7. 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 06; 14(2):453-62. PubMed ID: 17639058
    [Abstract] [Full Text] [Related]

  • 8. Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx.
    Gimm O.
    Fam Cancer; 2005 Jun 06; 4(1):17-23. PubMed ID: 15883706
    [Abstract] [Full Text] [Related]

  • 9. Genetic aspects of pheochromocytoma.
    Koch CA, Vortmeyer AO, Huang SC, Alesci S, Zhuang Z, Pacak K.
    Endocr Regul; 2001 Mar 06; 35(1):43-52. PubMed ID: 11308996
    [Abstract] [Full Text] [Related]

  • 10. Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene.
    Brauch H, Hoeppner W, Jähnig H, Wöhl T, Engelhardt D, Spelsberg F, Ritter MM.
    J Clin Endocrinol Metab; 1997 Dec 06; 82(12):4101-4. PubMed ID: 9398721
    [Abstract] [Full Text] [Related]

  • 11. 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 06; 157(1):55-62. PubMed ID: 19215943
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.
    Crossey PA, Eng C, Ginalska-Malinowska M, Lennard TW, Wheeler DC, Ponder BA, Maher ER.
    J Med Genet; 1995 Nov 01; 32(11):885-6. PubMed ID: 8592333
    [Abstract] [Full Text] [Related]

  • 14. Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes.
    Bar M, Friedman E, Jakobovitz O, Leibowitz G, Lerer I, Abeliovich D, Gross DJ.
    Clin Endocrinol (Oxf); 1997 Dec 01; 47(6):707-12. PubMed ID: 9497878
    [Abstract] [Full Text] [Related]

  • 15. Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.
    Kim JH, Seong MW, Lee KE, Choi HJ, Ku EJ, Bae JH, Park SS, Choi SH, Kim SW, Shin C, Kim SY.
    Clin Genet; 2014 Nov 01; 86(5):482-6. PubMed ID: 24134185
    [Abstract] [Full Text] [Related]

  • 16. 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 Nov 01; 61(1):43-8. PubMed ID: 20205103
    [Abstract] [Full Text] [Related]

  • 17. Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
    Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PL, O'Riordan JL, Toledo SP.
    J Med Genet; 1995 Dec 01; 32(12):934-7. PubMed ID: 8825918
    [Abstract] [Full Text] [Related]

  • 18. The pressure rises: update on the genetics of phaeochromocytoma.
    Maher ER, Eng C.
    Hum Mol Genet; 2002 Oct 01; 11(20):2347-54. PubMed ID: 12351569
    [Abstract] [Full Text] [Related]

  • 19. [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
    [Abstract] [Full Text] [Related]

  • 20. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
    Woodward ER, Eng C, McMahon R, Voutilainen R, Affara NA, Ponder BA, Maher ER.
    Hum Mol Genet; 1997 Jul 18; 6(7):1051-6. PubMed ID: 9215674
    [Abstract] [Full Text] [Related]

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