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Journal Abstract Search

498 related items for PubMed ID: 18031321

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  • 2. 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
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  • 3. 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 11; 7():1. PubMed ID: 16405730
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  • 4. 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 11; 41(6):805-14. PubMed ID: 20236688
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  • 5. 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 11; 10(8):457-61. PubMed ID: 12111639
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  • 9. 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 11; 26(7):1395-401. PubMed ID: 18551016
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  • 12. Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype.
    Chen F, Kishida T, Yao M, Hustad T, Glavac D, Dean M, Gnarra JR, Orcutt ML, Duh FM, Glenn G.
    Hum Mutat; 1995 Jul 11; 5(1):66-75. PubMed ID: 7728151
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  • 13. Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.
    Dannenberg H, van Nederveen FH, Abbou M, Verhofstad AA, Komminoth P, de Krijger RR, Dinjens WN.
    J Clin Oncol; 2005 Mar 20; 23(9):1894-901. PubMed ID: 15774781
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  • 14. Genetic basis of phaeochromocytoma and paraganglioma.
    Benn DE, Robinson BG.
    Best Pract Res Clin Endocrinol Metab; 2006 Sep 20; 20(3):435-50. PubMed ID: 16980204
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  • 16. New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.
    Bertherat J, Gimenez-Roqueplo AP.
    Horm Metab Res; 2005 Jun 20; 37(6):384-90. PubMed ID: 16001332
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  • 17. Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.
    Mora J, Cascón A, Robledo M, Catala A.
    Pediatr Blood Cancer; 2006 Nov 20; 47(6):785-9. PubMed ID: 16304664
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