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Acta Neuropathologica|August 20, 2013
Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signalingAlessandro Cama, Fabio Verginelli, Lavinia Vittoria Lotti, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 10, 2013
Epidemiology of autosomal-dominant polycystic kidney disease: an in-depth clinical study for south-western GermanyHartmut P H Neumann, Cordula Jilg, Janina Bacher, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 15, 2009
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patientsZoran Erlic, Lisa Rybicki, Mariola Peczkowska, et al.
Endocrine-Related Cancer|September 17, 2004
Malignant pheochromocytoma: current status and initiatives for future progressGraeme Eisenhofer, Stefan R Bornstein, Frederieke M Brouwers, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2009
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2Carsten C Boedeker, Zoran Erlic, Stéphane Richard, et al.
Endocrine-Related Cancer|October 31, 2013
Long-term prognosis of patients with pediatric pheochromocytomaBirke Bausch, Ulrich Wellner, Dirk Bausch, et al.
The New England Journal of Medicine|May 10, 2002
Germ-line mutations in nonsyndromic pheochromocytomaHartmut P H Neumann, Birke Bausch, Sarah R McWhinney, et al.
Endocrine-Related Cancer|January 18, 2015
A registry-based study of thyroid paraganglioma: histological and genetic characteristicsErnst von Dobschuetz, Helena Leijon, Camilla Schalin-Jäntti, et al.
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