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831 related items for PubMed ID: 24134185

  • 1. Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.
    Kim JH, Seong MW, Lee KE, Choi HJ, Ku EJ, Bae JH, Park SS, Choi SH, Kim SW, Shin C, Kim SY.
    Clin Genet; 2014 Nov; 86(5):482-6. PubMed ID: 24134185
    [Abstract] [Full Text] [Related]

  • 2. Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
    Pandit R, Khadilkar K, Sarathi V, Kasaliwal R, Goroshi M, Khare S, Nair S, Raghavan V, Dalvi A, Hira P, Fernandes G, Sathe P, Rojekar A, Malhotra G, Bakshi G, Prakash G, Bhansali A, Walia R, Kamalanathan S, Sahoo J, Desai A, Bhagwat N, Mappa P, Rajput R, Chandrashekhar SR, Shivane V, Menon P, Lila A, Bandgar T, Shah N.
    Eur J Endocrinol; 2016 Oct; 175(4):311-23. PubMed ID: 27539324
    [Abstract] [Full Text] [Related]

  • 3. Genetic testing in pheochromocytoma or functional paraganglioma.
    Amar L, Bertherat J, Baudin E, Ajzenberg C, Bressac-de Paillerets B, Chabre O, Chamontin B, Delemer B, Giraud S, Murat A, Niccoli-Sire P, Richard S, Rohmer V, Sadoul JL, Strompf L, Schlumberger M, Bertagna X, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP.
    J Clin Oncol; 2005 Dec 01; 23(34):8812-8. PubMed ID: 16314641
    [Abstract] [Full Text] [Related]

  • 4. 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 01; 14(2):453-62. PubMed ID: 17639058
    [Abstract] [Full Text] [Related]

  • 5. Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.
    Castellano M, Mori L, Giacchè M, Agliozzo E, Tosini R, Panarotto A, Cappelli C, Mulatero P, Cumetti D, Veglio F, Agabiti-Rosei E.
    Ann N Y Acad Sci; 2006 Aug 01; 1073():156-65. PubMed ID: 17102082
    [Abstract] [Full Text] [Related]

  • 6. Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden.
    Muth A, Abel F, Jansson S, Nilsson O, Ahlman H, Wängberg B.
    World J Surg; 2012 Jun 01; 36(6):1389-94. PubMed ID: 22270996
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  • 9. Semiquantitative 123I-Metaiodobenzylguanidine Scintigraphy to Distinguish Pheochromocytoma and Paraganglioma from Physiologic Adrenal Uptake and Its Correlation with Genotype-Dependent Expression of Catecholamine Transporters.
    van Berkel A, Rao JU, Lenders JW, Pellegata NS, Kusters B, Piscaer I, Hermus AR, Plantinga TS, Langenhuijsen JF, Vriens D, Janssen MJ, Gotthardt M, Timmers HJ.
    J Nucl Med; 2015 Jun 01; 56(6):839-46. PubMed ID: 25883126
    [Abstract] [Full Text] [Related]

  • 10. Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population.
    Choi H, Kim KJ, Hong N, Shin S, Choi JR, Kang SW, Lee ST, Rhee Y.
    Endocrinol Metab (Seoul); 2020 Dec 01; 35(4):858-872. PubMed ID: 33397040
    [Abstract] [Full Text] [Related]

  • 11. [Germline gene testing of the RET, VHL, SDHD and SDHB genes in patients with pheochromocytoma/paraganglioma].
    Wu K, Zhang Y, Zhang H, Tan ZH, Guo XH, Yang JM.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2018 Aug 18; 50(4):634-639. PubMed ID: 30122763
    [Abstract] [Full Text] [Related]

  • 12. Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
    Patócs A, Lendvai NK, Butz H, Liko I, Sapi Z, Szucs N, Toth G, Grolmusz VK, Igaz P, Toth M, Rácz K.
    Pathol Oncol Res; 2016 Oct 18; 22(4):673-9. PubMed ID: 26960314
    [Abstract] [Full Text] [Related]

  • 13. Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas.
    Krawczyk A, Hasse-Lazar K, Pawlaczek A, Szpak-Ulczok S, Krajewska J, Paliczka-Cieślak E, Jurecka-Lubieniecka B, Roskosz J, Chmielik E, Ziaja J, Cierpka L, Peczkowska M, Preibisz A, Januszewicz A, Otto M, Jarzab B.
    Endokrynol Pol; 2010 Oct 18; 61(1):43-8. PubMed ID: 20205103
    [Abstract] [Full Text] [Related]

  • 14. Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma.
    Jafri M, Whitworth J, Rattenberry E, Vialard L, Kilby G, Kumar AV, Izatt L, Lalloo F, Brennan P, Cook J, Morrison PJ, Canham N, Armstrong R, Brewer C, Tomkins S, Donaldson A, Barwell J, Cole TR, Atkinson AB, Aylwin S, Ball SG, Srirangalingam U, Chew SL, Evans DG, Hodgson SV, Irving R, Woodward E, Macdonald F, Maher ER.
    Clin Endocrinol (Oxf); 2013 Jun 18; 78(6):898-906. PubMed ID: 23072324
    [Abstract] [Full Text] [Related]

  • 15. 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, European-American Paraganglioma Study Group.
    JAMA; 2004 Aug 25; 292(8):943-51. PubMed ID: 15328326
    [Abstract] [Full Text] [Related]

  • 16. Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.
    Korpershoek E, Van Nederveen FH, Dannenberg H, Petri BJ, Komminoth P, Perren A, Lenders JW, Verhofstad AA, De Herder WW, De Krijger RR, Dinjens WN.
    Ann N Y Acad Sci; 2006 Aug 25; 1073():138-48. PubMed ID: 17102080
    [Abstract] [Full Text] [Related]

  • 17. Primary Renal Paragangliomas and Renal Neoplasia Associated with Pheochromocytoma/Paraganglioma: Analysis of von Hippel-Lindau (VHL), Succinate Dehydrogenase (SDHX) and Transmembrane Protein 127 (TMEM127).
    Gupta S, Zhang J, Milosevic D, Mills JR, Grebe SK, Smith SC, Erickson LA.
    Endocr Pathol; 2017 Sep 25; 28(3):253-268. PubMed ID: 28646318
    [Abstract] [Full Text] [Related]

  • 18. Genetics of pheochromocytoma and paraganglioma in Spanish patients.
    Cascón A, Pita G, Burnichon N, Landa I, López-Jiménez E, Montero-Conde C, Leskelä S, Leandro-García LJ, Letón R, Rodríguez-Antona C, Díaz JA, López-Vidriero E, González-Neira A, Velasco A, Matias-Guiu X, Gimenez-Roqueplo AP, Robledo M.
    J Clin Endocrinol Metab; 2009 May 25; 94(5):1701-5. PubMed ID: 19258401
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  • 19. 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]

  • 20. Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.
    Meyer-Rochow GY, Smith JM, Richardson AL, Marsh DJ, Sidhu SB, Robinson BG, Benn DE.
    J Surg Res; 2009 Nov 11; 157(1):55-62. PubMed ID: 19215943
    [Abstract] [Full Text] [Related]

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