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Hartmut P H Neumann

Showing results (61-70 of 132) with videos related to

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Radiology|January 31, 2002
Pheochromocytomas: detection with 18F DOPA whole body PET--initial resultsStefan Hoegerle, Egbert Nitzsche, Carsten Altehoefer, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytomaBirke Bausch, Ann-Cathrin Koschker, Martin Fassnacht, et al.
The New England Journal of Medicine|September 28, 2007
Evidence of MEN-2 in the original description of classic pheochromocytomaHartmut P H Neumann, Alexander Vortmeyer, Dieter Schmidt, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2005
Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneysMarkus Cybulla, Ellen Schaefer, Susanne Wendt, et al.
Clinical Endocrinology|April 5, 2013
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromesMariola Pęczkowska, Aldona Kowalska, Jacek Sygut, et al.
Familial Cancer|March 20, 2012
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-upC A Jilg, Hartmut P H Neumann, S Gläsker, et al.
Malaria Journal|February 4, 2010
Optimized high gradient magnetic separation for isolation of Plasmodium-infected red blood cellsSebastian C Bhakdi, Annette Ottinger, Sangdao Somsri, et al.
World Journal of Surgery|February 3, 2018
Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 PatientsMartin K Walz, Laura D Iova, Judith Deimel, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|February 26, 2013
Sequence variations in the von Hippel-Lindau tumor suppressor gene in patients with intracranial aneurysmsJan-Helge Klingler, Marie T Krüger, Johannes R Lemke, et al.
Human Molecular Genetics|November 24, 2012
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndromeElena Panizza, Tonino Ercolino, Luigi Mori, et al.
Pageof 14

Showing results (61-70 of 132) with videos related to

Sort By:
Pageof 14
Radiology|January 31, 2002
Pheochromocytomas: detection with 18F DOPA whole body PET--initial resultsStefan Hoegerle, Egbert Nitzsche, Carsten Altehoefer, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytomaBirke Bausch, Ann-Cathrin Koschker, Martin Fassnacht, et al.
The New England Journal of Medicine|September 28, 2007
Evidence of MEN-2 in the original description of classic pheochromocytomaHartmut P H Neumann, Alexander Vortmeyer, Dieter Schmidt, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2005
Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneysMarkus Cybulla, Ellen Schaefer, Susanne Wendt, et al.
Clinical Endocrinology|April 5, 2013
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromesMariola Pęczkowska, Aldona Kowalska, Jacek Sygut, et al.
Familial Cancer|March 20, 2012
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-upC A Jilg, Hartmut P H Neumann, S Gläsker, et al.
Malaria Journal|February 4, 2010
Optimized high gradient magnetic separation for isolation of Plasmodium-infected red blood cellsSebastian C Bhakdi, Annette Ottinger, Sangdao Somsri, et al.
World Journal of Surgery|February 3, 2018
Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 PatientsMartin K Walz, Laura D Iova, Judith Deimel, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|February 26, 2013
Sequence variations in the von Hippel-Lindau tumor suppressor gene in patients with intracranial aneurysmsJan-Helge Klingler, Marie T Krüger, Johannes R Lemke, et al.
Human Molecular Genetics|November 24, 2012
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndromeElena Panizza, Tonino Ercolino, Luigi Mori, et al.
Pageof 14