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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. Among authors: eng c. 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
Monogenetic hypertension and pheochromocytoma.
Neumann HP, Bender B, Zäuner I, Berger DP, Eng C, Brauch H, Zbar B. Neumann HP, et al. Among authors: eng c. Am J Kidney Dis. 1996 Sep;28(3):329-33. doi: 10.1016/s0272-6386(96)90488-6. Am J Kidney Dis. 1996. PMID: 8804229
Inherited pheochromocytoma.
Neumann HP, Bender BU, Januszewicz A, Janetschek G, Eng C. Neumann HP, et al. Among authors: eng c. Adv Nephrol Necker Hosp. 1997;27:361-76. Adv Nephrol Necker Hosp. 1997. PMID: 9408456 Review. No abstract available.
Case 13-2001: genetic testing in pheochromocytoma.
Neumann HP, Reincke M, Eng C. Neumann HP, et al. Among authors: eng c. N Engl J Med. 2001 Aug 16;345(7):547-8. N Engl J Med. 2001. PMID: 11519521 No abstract available.
Germ-line mutations in nonsyndromic pheochromocytoma.
Neumann HP, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith WM, Munk R, Manz T, Glaesker S, Apel TW, Treier M, Reineke M, Walz MK, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier-Woelfle M, Peçzkowska M, Szmigielski C, Eng C; Freiburg-Warsaw-Columbus Pheochromocytoma Study Group. Neumann HP, et al. Among authors: eng c. N Engl J Med. 2002 May 9;346(19):1459-66. doi: 10.1056/NEJMoa020152. N Engl J Med. 2002. PMID: 12000816 Free article.
1,912 results