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Radiology
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January 31, 2002
Pheochromocytomas: detection with 18F DOPA whole body PET--initial results
Stefan 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 pheochromocytoma
Birke 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 pheochromocytoma
Hartmut 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 kidneys
Markus 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 syndromes
Mariola 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-up
C 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 cells
Sebastian 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 Patients
Martin 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 aneurysms
Jan-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 syndrome
Elena Panizza, Tonino Ercolino, Luigi Mori, et al.
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Search research articles
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Showing results (61-70 of 132) with videos related to
Sort By:
Page
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Radiology
|
January 31, 2002
Pheochromocytomas: detection with 18F DOPA whole body PET--initial results
Stefan 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 pheochromocytoma
Birke 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 pheochromocytoma
Hartmut 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 kidneys
Markus 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 syndromes
Mariola 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-up
C 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 cells
Sebastian 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 Patients
Martin 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 aneurysms
Jan-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 syndrome
Elena Panizza, Tonino Ercolino, Luigi Mori, et al.
Page
of 14