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Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
Erlic Z, Rybicki L, Peczkowska M, Golcher H, Kann PH, Brauckhoff M, Müssig K, Muresan M, Schäffler A, Reisch N, Schott M, Fassnacht M, Opocher G, Klose S, Fottner C, Forrer F, Plöckinger U, Petersenn S, Zabolotny D, Kollukch O, Yaremchuk S, Januszewicz A, Walz MK, Eng C, Neumann HP; European-American Pheochromocytoma Study Group. Erlic Z, et al. Clin Cancer Res. 2009 Oct 15;15(20):6378-85. doi: 10.1158/1078-0432.CCR-09-1237. Epub 2009 Oct 13. Clin Cancer Res. 2009. PMID: 19825962
Familial nonsyndromic pheochromocytoma.
Opocher G, Schiavi F, Iacobone M, Toniato A, Sattarova S, Erlic Z, Martella M, Mian C, Merante Boschin I, Zambonin L, De Lazzari P, Murgia A, Pelizzo MR, Favia G, Mantero F. Opocher G, et al. Among authors: erlic z. Ann N Y Acad Sci. 2006 Aug;1073:149-55. doi: 10.1196/annals.1353.015. Ann N Y Acad Sci. 2006. PMID: 17102081
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.
Peczkowska M, Erlic Z, Hoffmann MM, Furmanek M, Cwikla J, Kubaszek A, Prejbisz A, Szutkowski Z, Kawecki A, Chojnowski K, Lewczuk A, Litwin M, Szyfter W, Walter MA, Sullivan M, Eng C, Januszewicz A, Neumann HP. Peczkowska M, et al. Among authors: erlic z. J Clin Endocrinol Metab. 2008 Dec;93(12):4818-25. doi: 10.1210/jc.2008-1290. Epub 2008 Sep 30. J Clin Endocrinol Metab. 2008. PMID: 18826997 Free PMC article.
[Pheochromocytoma - still a challenge].
Reisch N, Walz MK, Erlic Z, Neumann HP. Reisch N, et al. Among authors: erlic z. Internist (Berl). 2009 Jan;50(1):27-35. doi: 10.1007/s00108-008-2196-7. Internist (Berl). 2009. PMID: 19099277 Review. German.
Familial pheochromocytoma.
Erlic Z, Neumann HP. Erlic Z, et al. Hormones (Athens). 2009 Jan-Mar;8(1):29-38. doi: 10.14310/horm.2002.1219. Hormones (Athens). 2009. PMID: 19269919 Free article.
44 results