B. Bender

发表

A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency

H. Neumann, D. Schmidt, T. Quaschning, 2007, Clinical chemistry and laboratory medicine.

Preserved adrenocortical function after laparoscopic bilateral adrenal sparing surgery for hereditary pheochromocytoma.

H. Neumann, M. Reincke, G. Janetschek, 1999, The Journal of clinical endocrinology and metabolism.

Adrenal‐sparing surgery for phaeochromocytoma

H. Neumann, M. Reincke, J. Laubenberger, 1999, The British journal of surgery.

Monogenetic hypertension and pheochromocytoma.

H. Brauch, B. Zbar, C. Eng, 1996, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Clinical and genetic screening in patients with capillary retinal angioma

N. Bornfeld, H. Neumann, M. Foerster, 1999, Der Ophthalmologe.

Germ-line mutations in nonsyndromic pheochromocytoma.

J. Schipper, K. Zerres, C. Eng, 2002, The New England journal of medicine.

Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma.

H. Brauch, D. Glavač, W. Schultze‐Seemann, 1998, The Journal of urology.

Reconsideration of biallelic inactivation of theVHL tumour suppressor gene in hemangioblastomas of the central nervous system

J. Zentner, L. Mulligan, H. Neumann, 2001, Journal of neurology, neurosurgery, and psychiatry.

Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.

C. Eng, H. Neumann, S. Gläsker, 2000, The Journal of clinical endocrinology and metabolism.

VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality

M. Olschewski, C. Eng, H. Neumann, 2001, Journal of medical genetics.

An incidental finding--bilateral multifocal renal oncocytoma.

H. Neumann, P. Schollmeyer, B. Bender, 1997, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome.

H. Neumann, A. Januszewicz, R. Gärtner, 1997, The Journal of clinical endocrinology and metabolism.

Genotype–phenotype correlations in von hippel–lindau disease

H. Neumann, B. Bender, 1998, Journal of internal medicine.

The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical management.

W. Schultze‐Seemann, H. Neumann, A. Januszewicz, 1997, Contributions to nephrology.

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

D. Lenk, P. Zipfel, C. Skerka, 2003, Journal of medical genetics.

Germline Mutations in Non-syndromic Pheochromocytoma

J. Schipper, K. Zerres, C. Eng, 2004 .

The impact of molecular genetic analysis of theVHL gene in patients with haemangioblastomas of the central nervous system

J. Zentner, H. Neumann, V. van Velthoven, 1999, Journal of neurology, neurosurgery, and psychiatry.

Late occurrence of cysts in autosomal dominant medullary cystic kidney disease.

F. Hildebrandt, H. Neumann, P. Schollmeyer, 1997, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.