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 Neumann

Showing results (541-550 of 650) with videos related to

Pageof 65
Sort By:
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.
Central European Neurosurgery|March 16, 2010
Essentials and pitfalls in the treatment of CNS hemangioblastomas and von Hippel-Lindau diseaseS Gläsker, J H Klingler, K Müller, 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.
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.
Endocrinology|January 16, 2014
IGFBP2 is neither sufficient nor necessary for the physiological actions of leptin on glucose homeostasis in male ob/ob miceUrsula H Neumann, Sam Chen, Yuen Yi C Tam, 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.
Journal of Endocrinological Investigation|May 16, 2006
The malignant potential of a succinate dehydrogenase subunit B germline mutationC Fuentes, E Menéndez, J Pineda, 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.
Pageof 65

Showing results (541-550 of 650) with videos related to

Sort By:
Pageof 65
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.
Central European Neurosurgery|March 16, 2010
Essentials and pitfalls in the treatment of CNS hemangioblastomas and von Hippel-Lindau diseaseS Gläsker, J H Klingler, K Müller, 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.
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.
Endocrinology|January 16, 2014
IGFBP2 is neither sufficient nor necessary for the physiological actions of leptin on glucose homeostasis in male ob/ob miceUrsula H Neumann, Sam Chen, Yuen Yi C Tam, 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.
Journal of Endocrinological Investigation|May 16, 2006
The malignant potential of a succinate dehydrogenase subunit B germline mutationC Fuentes, E Menéndez, J Pineda, 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.
Pageof 65