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H P Neumann

Showing results (71-80 of 112) with videos related to

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Contributions to Nephrology|November 2, 2001
The challenge of kidney lesions in von Hippel-Lindau diseaseH P Neumann, P Riegler, W Huber, et al.
Deutsche Medizinische Wochenschrift (1946)|November 6, 1992
[Pheochromocytoma as dominant manifestation of v. Hippel-Lindau syndrome]H P Neumann, V Hofmann, I Zäuner, et al.
Clinical Endocrinology|January 1, 1997
Octreotide scintigraphy and catecholamine response to an octreotide challenge in malignant phaeochromocytomaD Kopf, A Bockisch, H Steinert, et al.
Klinische Monatsblatter Fur Augenheilkunde|November 17, 2009
[Family screening in patients with retinal angiomatosis]K-M Kreusel, L Krause, L Graul-Neumann, et al.
Urologia Internationalis|December 14, 2011
Growth kinetics in von Hippel-Lindau-associated renal cell carcinomaC A Jilg, H P Neumann, S Gläsker, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|August 4, 1998
Frequent progesterone receptor immunoreactivity in tuberous sclerosis-associated renal angiomyolipomasE P Henske, X Ao, M P Short, et al.
Genes, Chromosomes & Cancer|August 1, 1995
Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomasE P Henske, H P Neumann, B W Scheithauer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Tuberous sclerosis complex with end-stage renal failureH P Neumann, V Brüggen, D P Berger, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney diseaseR K Chatha, A M Johnson, P G Rothberg, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1990
Neuroendocrine sources of chromogranin-A in normal man: clues from selective stimulation of endocrine glandsM A Takiyyuddin, J H Cervenka, M R Pandian, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Contributions to Nephrology|November 2, 2001
The challenge of kidney lesions in von Hippel-Lindau diseaseH P Neumann, P Riegler, W Huber, et al.
Deutsche Medizinische Wochenschrift (1946)|November 6, 1992
[Pheochromocytoma as dominant manifestation of v. Hippel-Lindau syndrome]H P Neumann, V Hofmann, I Zäuner, et al.
Clinical Endocrinology|January 1, 1997
Octreotide scintigraphy and catecholamine response to an octreotide challenge in malignant phaeochromocytomaD Kopf, A Bockisch, H Steinert, et al.
Klinische Monatsblatter Fur Augenheilkunde|November 17, 2009
[Family screening in patients with retinal angiomatosis]K-M Kreusel, L Krause, L Graul-Neumann, et al.
Urologia Internationalis|December 14, 2011
Growth kinetics in von Hippel-Lindau-associated renal cell carcinomaC A Jilg, H P Neumann, S Gläsker, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|August 4, 1998
Frequent progesterone receptor immunoreactivity in tuberous sclerosis-associated renal angiomyolipomasE P Henske, X Ao, M P Short, et al.
Genes, Chromosomes & Cancer|August 1, 1995
Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomasE P Henske, H P Neumann, B W Scheithauer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Tuberous sclerosis complex with end-stage renal failureH P Neumann, V Brüggen, D P Berger, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney diseaseR K Chatha, A M Johnson, P G Rothberg, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1990
Neuroendocrine sources of chromogranin-A in normal man: clues from selective stimulation of endocrine glandsM A Takiyyuddin, J H Cervenka, M R Pandian, et al.
Pageof 12