BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 31279790)

  • 1. Management of Multiple Secreting Paragangliomas in a Succinate Dehydrogenase Subunit D (SDHD) Variant Carrier.
    Rijken JA; de Vos B; Leemans CR; Zwezerijnen GJCB; de Graaf P; Hensen EF; Dreijerink KMA; Dickhoff C; Symersky P
    Ann Thorac Surg; 2020 Feb; 109(2):e87-e90. PubMed ID: 31279790
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.
    Heesterman BL; Bayley JP; Tops CM; Hes FJ; van Brussel BT; Corssmit EP; Hamming JF; van der Mey AG; Jansen JC
    Eur J Hum Genet; 2013 Apr; 21(4):469-70. PubMed ID: 22948026
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: a founder effect?
    Lee SC; Chionh SB; Chong SM; Taschner PE
    Laryngoscope; 2003 Jun; 113(6):1055-8. PubMed ID: 12782822
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Succinate dehydrogenase-deficient tumors: diagnostic advances and clinical implications.
    Barletta JA; Hornick JL
    Adv Anat Pathol; 2012 Jul; 19(4):193-203. PubMed ID: 22692282
    [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. 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; 22(9):1358-64. PubMed ID: 12618761
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multifocal Paraganglioma and Pheochromocytoma Due to Truncated SDHD Mutation.
    Zuo Y; Li X; Wu X; Zhou J; Wang J; Wang J; Wu Z; Li H; Zhang X
    Urology; 2018 Jun; 116():63-67. PubMed ID: 29545045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. No difference in phenotype of the main Dutch SDHD founder mutations.
    van Hulsteijn LT; den Dulk AC; Hes FJ; Bayley JP; Jansen JC; Corssmit EP
    Clin Endocrinol (Oxf); 2013 Dec; 79(6):824-31. PubMed ID: 23586964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trimodal (18)F-DOPA PET/CT/MR fusion imaging for optimal restaging of head and neck paragangliomas in a SDHD mutation carrier.
    Treglia G; Ruberto T; Giovanella L
    Endocrine; 2016 May; 52(2):397-8. PubMed ID: 25860886
    [No Abstract]   [Full Text] [Related]  

  • 12. Paragangliomas in patients with mutations of the SDHD gene.
    Boedeker CC; Neumann HP; Ridder GJ; Maier W; Schipper J
    Otolaryngol Head Neck Surg; 2005 Mar; 132(3):467-70. PubMed ID: 15746863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. R46Q mutation in the succinate dehydrogenase B gene (SDHB) in a Japanese family with both abdominal and thoracic paraganglioma following metastasis.
    Takekoshi K; Isobe K; Suzuki H; Nissato S; Kawakami Y; Kawai K; Yamada N
    Endocr J; 2008 May; 55(2):299-303. PubMed ID: 18362451
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Predominant expression of mutated allele of the succunate dehydrogenase D (SDHD) gene in the SDHD-related paragangliomas.
    Yamashita R; Usui T; Hashimoto S; Suzuki H; Takahashi M; Honkura K; Iwamoto K; Kodama E; Tagami T; Naruse M; Shimatsu A; Kaise K
    Endocr J; 2009; 56(9):1129-35. PubMed ID: 19550080
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
    Schiavi F; Boedeker CC; Bausch B; Peçzkowska M; Gomez CF; Strassburg T; Pawlu C; Buchta M; Salzmann M; Hoffmann MM; Berlis A; Brink I; Cybulla M; Muresan M; Walter MA; Forrer F; Välimäki M; Kawecki A; Szutkowski Z; Schipper J; Walz MK; Pigny P; Bauters C; Willet-Brozick JE; Baysal BE; Januszewicz A; Eng C; Opocher G; Neumann HP;
    JAMA; 2005 Oct; 294(16):2057-63. PubMed ID: 16249420
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
    Piccini V; Rapizzi E; Bacca A; Di Trapani G; Pulli R; Giachè V; Zampetti B; Lucci-Cordisco E; Canu L; Corsini E; Faggiano A; Deiana L; Carrara D; Tantardini V; Mariotti S; Ambrosio MR; Zatelli MC; Parenti G; Colao A; Pratesi C; Bernini G; Ercolino T; Mannelli M
    Endocr Relat Cancer; 2012 Apr; 19(2):149-55. PubMed ID: 22241717
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SDHAF2 (PGL2-SDH5) and hereditary head and neck paraganglioma.
    Kunst HP; Rutten MH; de Mönnink JP; Hoefsloot LH; Timmers HJ; Marres HA; Jansen JC; Kremer H; Bayley JP; Cremers CW
    Clin Cancer Res; 2011 Jan; 17(2):247-54. PubMed ID: 21224366
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
    Klein RD; Jin L; Rumilla K; Young WF; Lloyd RV
    Diagn Mol Pathol; 2008 Jun; 17(2):94-100. PubMed ID: 18382370
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unusual case of Cowden-like syndrome, neck paraganglioma, and pituitary adenoma.
    Efstathiadou ZA; Sapranidis M; Anagnostis P; Kita MD
    Head Neck; 2014 Jan; 36(1):E12-6. PubMed ID: 23804288
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.