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Journal Abstract Search

1177 related items for PubMed ID: 12618761

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  • 2. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.
    Astuti D, Hart-Holden N, Latif F, Lalloo F, Black GC, Lim C, Moran A, Grossman AB, Hodgson SV, Freemont A, Ramsden R, Eng C, Evans DG, Maher ER.
    Clin Endocrinol (Oxf); 2003 Dec; 59(6):728-33. PubMed ID: 14974914
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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; 10(8):457-61. PubMed ID: 12111639
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  • 6. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.
    Gimm O, Armanios M, Dziema H, Neumann HP, Eng C.
    Cancer Res; 2000 Dec 15; 60(24):6822-5. PubMed ID: 11156372
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  • 10. An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years.
    Elston MS, Benn D, Robinson BG, Conaglen JV.
    Intern Med J; 2006 Feb 15; 36(2):129-31. PubMed ID: 16472267
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  • 11. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.
    Bayley JP, Kunst HP, Cascon A, Sampietro ML, Gaal J, Korpershoek E, Hinojar-Gutierrez A, Timmers HJ, Hoefsloot LH, Hermsen MA, Suárez C, Hussain AK, Vriends AH, Hes FJ, Jansen JC, Tops CM, Corssmit EP, de Knijff P, Lenders JW, Cremers CW, Devilee P, Dinjens WN, de Krijger RR, Robledo M.
    Lancet Oncol; 2010 Apr 15; 11(4):366-72. PubMed ID: 20071235
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  • 12. 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 15; 26(7):1395-401. PubMed ID: 18551016
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  • 13. Novel germline mutations in the SDHB and SDHD genes in Japanese pheochromocytomas.
    Isobe K, Minowada S, Tatsuno I, Suzukawa K, Nissato S, Nanmoku T, Hara H, Yashiro T, Kawakami Y, Takekoshi K.
    Horm Res; 2007 Jul 15; 68(2):68-71. PubMed ID: 17308434
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  • 14. Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?
    Cascón A, Montero-Conde C, Ruiz-Llorente S, Mercadillo F, Letón R, Rodríguez-Antona C, Martínez-Delgado B, Delgado M, Díez A, Rovira A, Díaz JA, Robledo M.
    Genes Chromosomes Cancer; 2006 Mar 15; 45(3):213-9. PubMed ID: 16258955
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  • 15. SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.
    Douwes Dekker PB, Hogendoorn PC, Kuipers-Dijkshoorn N, Prins FA, van Duinen SG, Taschner PE, van der Mey AG, Cornelisse CJ.
    J Pathol; 2003 Nov 15; 201(3):480-6. PubMed ID: 14595761
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  • 16. Familial paraganglioma syndromes.
    Chetty R.
    J Clin Pathol; 2010 Jun 15; 63(6):488-91. PubMed ID: 20498024
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  • 17. [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 16; 146(46):2188-90. PubMed ID: 12467161
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  • 18. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
    van Nederveen FH, Gaal J, Favier J, Korpershoek E, Oldenburg RA, de Bruyn EM, Sleddens HF, Derkx P, Rivière J, Dannenberg H, Petri BJ, Komminoth P, Pacak K, Hop WC, Pollard PJ, Mannelli M, Bayley JP, Perren A, Niemann S, Verhofstad AA, de Bruïne AP, Maher ER, Tissier F, Méatchi T, Badoual C, Bertherat J, Amar L, Alataki D, Van Marck E, Ferrau F, François J, de Herder WW, Peeters MP, van Linge A, Lenders JW, Gimenez-Roqueplo AP, de Krijger RR, Dinjens WN.
    Lancet Oncol; 2009 Aug 16; 10(8):764-71. PubMed ID: 19576851
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  • 19. The genetics of paragangliomas: a review.
    Martin TP, Irving RM, Maher ER.
    Clin Otolaryngol; 2007 Feb 16; 32(1):7-11. PubMed ID: 17298303
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  • 20. 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 16; 41(6):805-14. PubMed ID: 20236688
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