Hartmut P. H. Neumann
Department of Nephrology
Albert Ludwigs University
Freiburg
Germany
Name/email consistency: high
- New genetic causes of pheochromocytoma: current concepts and the clinical relevance. Neumann, H.P., Cybulla, M., Shibata, H., Oya, M., Naruse, M., Higashihara, E., Terachi, T., Ling, H., Takami, H., Shuin, T., Murai, M. Keio. J. Med (2005)
- How many pathways to pheochromocytoma?. Neumann, H.P., Hoegerle, S., Manz, T., Brenner, K., Iliopoulos, O. Semin. Nephrol. (2002)
- Germ-line mutations in nonsyndromic pheochromocytoma. Neumann, H.P., Bausch, B., McWhinney, S.R., Bender, B.U., Gimm, O., Franke, G., Schipper, J., Klisch, J., Altehoefer, C., Zerres, K., Januszewicz, A., Eng, C., Smith, W.M., Munk, R., Manz, T., Glaesker, S., Apel, T.W., Treier, M., Reineke, M., Walz, M.K., Hoang-Vu, C., Brauckhoff, M., Klein-Franke, A., Klose, P., Schmidt, H., Maier-Woelfle, M., Peçzkowska, M., Szmigielski, C., Eng, C. N. Engl. J. Med. (2002)
- The challenge of kidney lesions in von Hippel-Lindau disease. Neumann, H.P., Riegler, P., Huber, W., Corradini, R., Sessa, A., Fontana, D., Wetterauer, U., Janetschek, G. Contrib. Nephrol (2001)
- Preserved adrenocortical function after laparoscopic bilateral adrenal sparing surgery for hereditary pheochromocytoma. Neumann, H.P., Reincke, M., Bender, B.U., Elsner, R., Janetschek, G. J. Clin. Endocrinol. Metab. (1999)
- Genotype-phenotype correlations in von Hippel-Lindau disease. Neumann, H.P., Bender, B.U. J. Intern. Med. (1998)
- The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical management. Neumann, H.P., Bender, B.U., Schultze-Seemann, W., Krause, T., Altehoefer, C., Scheremet, R., Orszagh, M., Schwarzkopf, G., Januszewicz, A., Janetschek, G., Riegler, P. Contrib. Nephrol (1997)