Authors: Frenzel, S Apel, TW Heidemann, PH Zerres, K Neumann, HPH Dorr, HG

Citation: S. Frenzel et al., Phaeochromocytoma associated with a de novo VHL mutation as form fruste ofvon Hippel-Lindau disease, EUR J PED, 160(7), 2001, pp. 421-424

Authors: Abel, KB Apel, TW Beck, M Neumann, HPH

Citation: Kb. Abel et al., Fabry's disease, NIEREN HOCH, 30(6), 2001, pp. 261-266

Authors: Neumann, HPH Schulenburg, S Apel, TW

Citation: Hph. Neumann et al., Familial renal tumors in adults, NIEREN HOCH, 30(6), 2001, pp. 267-277

Authors: Glasker, S Bender, BU Apel, TW van Velthoven, V Mulligan, LM Zentner, J Neumann, NPH

Citation: S. Glasker et al., Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system, J NE NE PSY, 70(5), 2001, pp. 644-648

Authors: Januszewicz, A Neumann, HPH Lon, I Szmigielski, C Symonides, B Kabat, M Apel, TW Wocial, B Lapinski, M Januszewicz, W

Citation: A. Januszewicz et al., Incidence and clinical relevance of RET proto-oncogene germline mutations in pheochromocytoma patients, J HYPERTENS, 18(8), 2000, pp. 1019-1023

Authors: Glasker, S Bender, BU Apel, TW Natt, E van Velthoven, V Scheremet, R Zentner, J Neumann, HPH

Citation: S. Glasker et al., The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system, J NE NE PSY, 67(6), 1999, pp. 758-762