Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H P Neumann

Showing results (51-60 of 112) with videos related to

Pageof 12
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1991
Serum erythropoietin levels in von Hippel-Lindau syndromeH P Neumann, P Schollmeyer, H R Eggert, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 10, 2001
A patient with neurological deficits and seizures after renal transplantationT Manz, W Grotz, M Orszagh, et al.
Klinische Wochenschrift|October 15, 1985
Mild proteinuria in patients with unilateral kidneyG Oberle, H P Neumann, P Schollmeyer, et al.
The British Journal of Surgery|February 23, 1999
Adrenal-sparing surgery for phaeochromocytomaH P Neumann, B U Bender, M Reincke, et al.
Human Molecular Genetics|February 5, 1999
Expression of the von Hippel-Lindau-binding protein-1 (Vbp1) in fetal and adult mouse tissuesM Hemberger, H Himmelbauer, H P Neumann, et al.
Human Molecular Genetics|July 21, 1998
Gene conversion is a likely cause of mutation in PKD1T J Watnick, M A Gandolph, H Weber, et al.
Deutsche Medizinische Wochenschrift (1946)|October 25, 1996
[Primary pigmented nodular adrenocortical dysplasia. A rare cause of Cushing's syndrome]K Anding, G Köhler, N Böhm, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1996
Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel-Lindau syndromeG Kempermann, H P Neumann, R Scheremet, et al.
Human Genetics|May 1, 1989
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndromeM Kiechle-Schwarz, H P Neumann, H J Decker, et al.
Cancer Genetics and Cytogenetics|June 1, 1989
Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndromeH J Decker, R M Gemmill, H P Neumann, et al.
Pageof 12

Showing results (51-60 of 112) with videos related to

Sort By:
Pageof 12
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1991
Serum erythropoietin levels in von Hippel-Lindau syndromeH P Neumann, P Schollmeyer, H R Eggert, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 10, 2001
A patient with neurological deficits and seizures after renal transplantationT Manz, W Grotz, M Orszagh, et al.
Klinische Wochenschrift|October 15, 1985
Mild proteinuria in patients with unilateral kidneyG Oberle, H P Neumann, P Schollmeyer, et al.
The British Journal of Surgery|February 23, 1999
Adrenal-sparing surgery for phaeochromocytomaH P Neumann, B U Bender, M Reincke, et al.
Human Molecular Genetics|February 5, 1999
Expression of the von Hippel-Lindau-binding protein-1 (Vbp1) in fetal and adult mouse tissuesM Hemberger, H Himmelbauer, H P Neumann, et al.
Human Molecular Genetics|July 21, 1998
Gene conversion is a likely cause of mutation in PKD1T J Watnick, M A Gandolph, H Weber, et al.
Deutsche Medizinische Wochenschrift (1946)|October 25, 1996
[Primary pigmented nodular adrenocortical dysplasia. A rare cause of Cushing's syndrome]K Anding, G Köhler, N Böhm, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1996
Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel-Lindau syndromeG Kempermann, H P Neumann, R Scheremet, et al.
Human Genetics|May 1, 1989
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndromeM Kiechle-Schwarz, H P Neumann, H J Decker, et al.
Cancer Genetics and Cytogenetics|June 1, 1989
Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndromeH J Decker, R M Gemmill, H P Neumann, et al.
Pageof 12