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Journal Abstract Search


552 related items for PubMed ID: 12467161

  • 1. [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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  • 5. 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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  • 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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  • 7. 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 Dec 15; 68(2):68-71. PubMed ID: 17308434
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  • 8. 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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  • 11. Germline SDHD mutation in paraganglioma of the spinal cord.
    Masuoka J, Brandner S, Paulus W, Soffer D, Vital A, Chimelli L, Jouvet A, Yonekawa Y, Kleihues P, Ohgaki H.
    Oncogene; 2001 Aug 16; 20(36):5084-6. PubMed ID: 11526495
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  • 13. Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas.
    Kytölä S, Nord B, Elder EE, Carling T, Kjellman M, Cedermark B, Juhlin C, Höög A, Isola J, Larsson C.
    Genes Chromosomes Cancer; 2002 Jul 16; 34(3):325-32. PubMed ID: 12007193
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  • 16. 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 16; 26(7):1395-401. PubMed ID: 18551016
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  • 17. 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 16; 10(8):457-61. PubMed ID: 12111639
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  • 18. Clinical and molecular progress in hereditary paraganglioma.
    Baysal BE.
    J Med Genet; 2008 Nov 16; 45(11):689-94. PubMed ID: 18978332
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  • 19. Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
    Lefebvre S, Borson-Chazot F, Boutry-Kryza N, Wion N, Schillo F, Peix JL, Brunaud L, Finat A, Calender A, Giraud S.
    Horm Metab Res; 2012 May 16; 44(5):334-8. PubMed ID: 22517554
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  • 20. 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; 16(2):527-36. PubMed ID: 19289533
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