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Journal Abstract Search

1122 related items for PubMed ID: 20236688

  • 1. 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; 41(6):805-14. PubMed ID: 20236688
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. 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 11; 45(3):213-9. PubMed ID: 16258955
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  • 5. 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 Mar 11; 68(2):68-71. PubMed ID: 17308434
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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients.
    Bayley JP, Weiss MM, Grimbergen A, van Brussel BT, Hes FJ, Jansen JC, Verhoef S, Devilee P, Corssmit EP, Vriends AH.
    Endocr Relat Cancer; 2009 Sep 06; 16(3):929-37. PubMed ID: 19546167
    [Abstract] [Full Text] [Related]

  • 8. 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 06; 10(8):764-71. PubMed ID: 19576851
    [Abstract] [Full Text] [Related]

  • 9. Usefulness of Succinate dehydrogenase B (SDHB) immunohistochemistry in guiding mutational screening among patients with pheochromocytoma-paraganglioma syndromes.
    Pai R, Manipadam MT, Singh P, Ebenazer A, Samuel P, Rajaratnam S.
    APMIS; 2014 Nov 06; 122(11):1130-5. PubMed ID: 24735130
    [Abstract] [Full Text] [Related]

  • 10. Succinate dehydrogenase (SDH) and mitochondrial driven neoplasia.
    Gill AJ.
    Pathology; 2012 Jun 06; 44(4):285-92. PubMed ID: 22544211
    [Abstract] [Full Text] [Related]

  • 11. 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 06; 26(7):1395-401. PubMed ID: 18551016
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  • 13. 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 06; 17(2):94-100. PubMed ID: 18382370
    [Abstract] [Full Text] [Related]

  • 14. Potential Pitfalls of SDH Immunohistochemical Detection in Paragangliomas and Phaeochromocytomas Harbouring Germline SDHx Gene Mutation.
    Santi R, Rapizzi E, Canu L, Ercolino T, Baroni G, Fucci R, Costa G, Mannelli M, Nesi G.
    Anticancer Res; 2017 Feb 06; 37(2):805-812. PubMed ID: 28179334
    [Abstract] [Full Text] [Related]

  • 15. Usefulness of negative and weak-diffuse pattern of SDHB immunostaining in assessment of SDH mutations in paragangliomas and pheochromocytomas.
    Castelblanco E, Santacana M, Valls J, de Cubas A, Cascón A, Robledo M, Matias-Guiu X.
    Endocr Pathol; 2013 Dec 06; 24(4):199-205. PubMed ID: 24096807
    [Abstract] [Full Text] [Related]

  • 16. 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 06; 10(8):457-61. PubMed ID: 12111639
    [Abstract] [Full Text] [Related]

  • 17. Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.
    Ercolino T, Becherini L, Valeri A, Maiello M, Gaglianò MS, Parenti G, Ramazzotti M, Piscitelli E, Simi L, Pinzani P, Nesi G, Degl'Innocenti D, Console N, Bergamini C, Mannelli M.
    Clin Endocrinol (Oxf); 2008 May 06; 68(5):762-8. PubMed ID: 18031321
    [Abstract] [Full Text] [Related]

  • 18. SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma.
    Menara M, Oudijk L, Badoual C, Bertherat J, Lepoutre-Lussey C, Amar L, Iturrioz X, Sibony M, Zinzindohoué F, de Krijger R, Gimenez-Roqueplo AP, Favier J.
    J Clin Endocrinol Metab; 2015 Feb 06; 100(2):E287-91. PubMed ID: 25405498
    [Abstract] [Full Text] [Related]

  • 19. Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma.
    Korpershoek E, Petri BJ, van Nederveen FH, Dinjens WN, Verhofstad AA, de Herder WW, Schmid S, Perren A, Komminoth P, de Krijger RR.
    Endocr Relat Cancer; 2007 Jun 06; 14(2):453-62. PubMed ID: 17639058
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