BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

557 related articles for article (PubMed ID: 11897817)

  • 21. 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]  

  • 22. Germline mutations and genotype-phenotype associations in head and neck paraganglioma patients with negative family history in China.
    Zhu WD; Wang ZY; Chai YC; Wang XW; Chen DY; Wu H
    Eur J Med Genet; 2015 Sep; 58(9):433-8. PubMed ID: 26096992
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.
    Dannenberg H; Dinjens WN; Abbou M; Van Urk H; Pauw BK; Mouwen D; Mooi WJ; de Krijger RR
    Clin Cancer Res; 2002 Jul; 8(7):2061-6. PubMed ID: 12114404
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
    Neumann HP; Pawlu C; Peczkowska M; Bausch B; McWhinney SR; Muresan M; Buchta M; Franke G; Klisch J; Bley TA; Hoegerle S; Boedeker CC; Opocher G; Schipper J; Januszewicz A; Eng C;
    JAMA; 2004 Aug; 292(8):943-51. PubMed ID: 15328326
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. A novel succinate dehydrogenase subunit B germline variant associated with head and neck paraganglioma in a Dutch kindred: A family-based study.
    de Vos B; Rijken JA; Adank MA; Hoksbergen AWJ; Bayley JP; Leemans CR; Hensen EF
    Clin Otolaryngol; 2018 Jun; 43(3):841-845. PubMed ID: 29292578
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X.
    Simi L; Sestini R; Ferruzzi P; Gaglianò MS; Gensini F; Mascalchi M; Guerrini L; Pratesi C; Pinzani P; Nesi G; Ercolino T; Genuardi M; Mannelli M
    J Med Genet; 2005 Aug; 42(8):e52. PubMed ID: 16061558
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel G106D alteration of the SDHD gene in a pedigree with familial paraganglioma.
    Ogawa K; Shiga K; Saijo S; Ogawa T; Kimura N; Horii A
    Am J Med Genet A; 2006 Nov; 140(22):2441-6. PubMed ID: 17041923
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paraganglioma.
    Bayley JP; Bausch B; Rijken JA; van Hulsteijn LT; Jansen JC; Ascher D; Pires DEV; Hes FJ; Hensen EF; Corssmit EPM; Devilee P; Neumann HPH
    J Med Genet; 2020 Feb; 57(2):96-103. PubMed ID: 31492822
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of three new variants of SDHx genes in a cohort of Portuguese patients with extra-adrenal paragangliomas.
    Domingues R; Montalvão P; Magalhães M; Santos R; Duarte L; Bugalho MJ
    J Endocrinol Invest; 2012 Dec; 35(11):975-80. PubMed ID: 22293219
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
    Burnichon N; Rohmer V; Amar L; Herman P; Leboulleux S; Darrouzet V; Niccoli P; Gaillard D; Chabrier G; Chabolle F; Coupier I; Thieblot P; Lecomte P; Bertherat J; Wion-Barbot N; Murat A; Venisse A; Plouin PF; Jeunemaitre X; Gimenez-Roqueplo AP;
    J Clin Endocrinol Metab; 2009 Aug; 94(8):2817-27. PubMed ID: 19454582
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma.
    McWhinney SR; Pilarski RT; Forrester SR; Schneider MC; Sarquis MM; Dias EP; Eng C
    J Clin Endocrinol Metab; 2004 Nov; 89(11):5694-9. PubMed ID: 15531530
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutation analysis of the SDHB and SDHD genes in pheochromocytomas and paragangliomas: identification of a novel nonsense mutation (Q168X) in the SDHB gene.
    Oishi Y; Nagai S; Yoshida M; Fujisawa S; Sazawa A; Shinohara N; Nonomura K; Matsuno K; Shimizu C
    Endocr J; 2010; 57(8):745-50. PubMed ID: 20505258
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria.
    Janecke AR; Willett-Brozick JE; Karas C; Hasipek M; Loeffler-Ragg J; Baysal BE
    J Hum Genet; 2010 Mar; 55(3):182-5. PubMed ID: 20111059
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. SDHx gene detection and clinical Phenotypic analysis of multiple paraganglioma in the head and neck.
    Ding Y; Feng Y; Wells M; Huang Z; Chen X
    Laryngoscope; 2019 Feb; 129(2):E67-E71. PubMed ID: 30484866
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.
    Cascon A; Ruiz-Llorente S; Cebrian A; Telleria D; Rivero JC; Diez JJ; Lopez-Ibarra PJ; Jaunsolo MA; Benitez J; Robledo M
    Eur J Hum Genet; 2002 Aug; 10(8):457-61. PubMed ID: 12111639
    [TBL] [Abstract][Full Text] [Related]  

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

  • 40. Reduced Risk of Corporal Tumors in Patients With Head and Neck Paragangliomas With p.Pro81Leu Mutations.
    Miller KM; Sbeih F; Contrera K; Reddy CA; Marquard J; Eng C; Lorenz RR
    Otolaryngol Head Neck Surg; 2023 Sep; 169(3):570-576. PubMed ID: 36939592
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 28.