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Page 1
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. N Engl J Med. 2002 May 9;346(19):1459-66. doi: 10.1056/NEJMoa020152. N Engl J Med. 2002. PMID: 12000816 Free article.
Pheochromocytoma: presentation, diagnosis and treatment.
Reisch N, Peczkowska M, Januszewicz A, Neumann HP. Reisch N, et al. Among authors: neumann hp. J Hypertens. 2006 Dec;24(12):2331-9. doi: 10.1097/01.hjh.0000251887.01885.54. J Hypertens. 2006. PMID: 17082709 Review.
Inherited pheochromocytoma.
Neumann HP, Bender BU, Januszewicz A, Janetschek G, Eng C. Neumann HP, et al. Adv Nephrol Necker Hosp. 1997;27:361-76. Adv Nephrol Necker Hosp. 1997. PMID: 9408456 Review. No abstract available.
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
Pęczkowska M, Kowalska A, Sygut J, Waligórski D, Malinoc A, Janaszek-Sitkowska H, Prejbisz A, Januszewicz A, Neumann HP. Pęczkowska M, et al. Among authors: neumann hp. Clin Endocrinol (Oxf). 2013 Dec;79(6):817-23. doi: 10.1111/cen.12218. Epub 2013 May 3. Clin Endocrinol (Oxf). 2013. PMID: 23551045
The genetic basis of pheochromocytoma.
Gimm O, Koch CA, Januszewicz A, Opocher G, Neumann HP. Gimm O, et al. Among authors: neumann hp. Front Horm Res. 2004;31:45-60. doi: 10.1159/000074657. Front Horm Res. 2004. PMID: 14674304 Review.
289 results