BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

281 related articles for article (PubMed ID: 17936061)

  • 1. Screening for familial paragangliomas.
    Myssiorek D; Ferlito A; Silver CE; Rodrigo JP; Baysal BE; Fagan JJ; Suárez C; Rinaldo A
    Oral Oncol; 2008 Jun; 44(6):532-7. PubMed ID: 17936061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas.
    Mhatre AN; Li Y; Feng L; Gasperin A; Lalwani AK
    Clin Genet; 2004 Nov; 66(5):461-6. PubMed ID: 15479192
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High prevalence of SDHB mutations in head and neck paraganglioma in Belgium.
    Persu A; Hamoir M; Grégoire V; Garin P; Duvivier E; Reychler H; Chantrain G; Mortier G; Mourad M; Maiter D; Vikkula M
    J Hypertens; 2008 Jul; 26(7):1395-401. PubMed ID: 18551016
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The genetics of paragangliomas: a review.
    Martin TP; Irving RM; Maher ER
    Clin Otolaryngol; 2007 Feb; 32(1):7-11. PubMed ID: 17298303
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Malignant head and neck paragangliomas in SDHB mutation carriers.
    Boedeker CC; Neumann HP; Maier W; Bausch B; Schipper J; Ridder GJ
    Otolaryngol Head Neck Surg; 2007 Jul; 137(1):126-9. PubMed ID: 17599579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment.
    Renard L; Godfraind C; Boon LM; Vikkula M
    Head Neck; 2003 Feb; 25(2):146-51. PubMed ID: 12509798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
    Taschner PE; Bröcker-Vriends AH; van der Mey AG
    Ned Tijdschr Geneeskd; 2002 Nov; 146(46):2188-90. PubMed ID: 12467161
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
    Bayley JP; van Minderhout I; Weiss MM; Jansen JC; Oomen PH; Menko FH; Pasini B; Ferrando B; Wong N; Alpert LC; Williams R; Blair E; Devilee P; Taschner PE
    BMC Med Genet; 2006 Jan; 7():1. PubMed ID: 16405730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management.
    Bikhazi PH; Roeder E; Attaie A; Lalwani AK
    Am J Otol; 1999 Sep; 20(5):639-43. PubMed ID: 10503587
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
    Taschner PE; Jansen JC; Baysal BE; Bosch A; Rosenberg EH; Bröcker-Vriends AH; van Der Mey AG; van Ommen GJ; Cornelisse CJ; Devilee P
    Genes Chromosomes Cancer; 2001 Jul; 31(3):274-81. PubMed ID: 11391798
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications.
    Prontera P; Ferrando B; Giuliani V; Falcinelli F; Mencarelli A; Rogaia D; Pasini B; Donti E
    Genet Couns; 2008; 19(4):413-8. PubMed ID: 19239085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic and molecular bases of paragangliomas].
    Núñez Lozano M; González Sarmiento R
    Acta Otorrinolaringol Esp; 2009 Feb; 60 Suppl 1():24-8. PubMed ID: 19245772
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial paraganglioma syndrome: applying genetic screening in otolaryngology.
    Dziegielewski PT; Knox A; Liu R; Hung RW; Harris J
    J Otolaryngol Head Neck Surg; 2010 Dec; 39(6):646-53. PubMed ID: 21144359
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular progress in hereditary paraganglioma.
    Baysal BE
    J Med Genet; 2008 Nov; 45(11):689-94. PubMed ID: 18978332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
    Baysal BE; Willett-Brozick JE; Lawrence EC; Drovdlic CM; Savul SA; McLeod DR; Yee HA; Brackmann DE; Slattery WH; Myers EN; Ferrell RE; Rubinstein WS
    J Med Genet; 2002 Mar; 39(3):178-83. PubMed ID: 11897817
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.
    Havekes B; van der Klaauw AA; Weiss MM; Jansen JC; van der Mey AG; Vriends AH; Bonsing BA; Romijn JA; Corssmit EP
    Endocr Relat Cancer; 2009 Jun; 16(2):527-36. PubMed ID: 19289533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Malignant paraganglioma caused by a novel germline mutation of the succinate dehydrogenase D-gene--a case report.
    Papaspyrou K; Rossmann H; Fottner C; Weber MM; Mann W; Lackner KJ; Helling K
    Head Neck; 2008 Jul; 30(7):964-9. PubMed ID: 18213727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients.
    Hensen EF; Siemers MD; Jansen JC; Corssmit EP; Romijn JA; Tops CM; van der Mey AG; Devilee P; Cornelisse CJ; Bayley JP; Vriends AH
    Clin Endocrinol (Oxf); 2011 Nov; 75(5):650-5. PubMed ID: 21561462
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Paragangliomas and paraganglioma syndromes].
    Boedeker CC
    Laryngorhinootologie; 2011 Mar; 90 Suppl 1():S56-82. PubMed ID: 21523634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Head and neck paragangliomas: revision of 89 cases in 73 patients].
    Sevilla García MA; Llorente Pendás JL; Rodrigo Tapia JP; García Rostán G; Suárez Fente V; Coca Pelaz A; Suárez Nieto C
    Acta Otorrinolaringol Esp; 2007 Mar; 58(3):94-100. PubMed ID: 17371691
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.