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Hartmut P H Neumann

Showing results (91-100 of 117) with videos related to

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Cerebrovascular Diseases Extra|November 10, 2012
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney diseaseHartmut P H Neumann, Angelica Malinoc, Janina Bacher, et al.
American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.
Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2012
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expressionFrancesca Schiavi, Serena Demattè, Maria Enrica Cecchini, et al.
Annals of Human Genetics|September 13, 2011
Age-related penetrance of hereditary atypical hemolytic uremic syndromeMaren Sullivan, Lisa A Rybicki, Aurelia Winter, et al.
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.
Neuroendocrinology|March 21, 2015
Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed TomographyIlona Michałowska, Jarosław B Ćwikła, Mariola Pęczkowska, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Cerebrovascular Diseases Extra|November 10, 2012
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney diseaseHartmut P H Neumann, Angelica Malinoc, Janina Bacher, et al.
American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.
Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2012
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expressionFrancesca Schiavi, Serena Demattè, Maria Enrica Cecchini, et al.
Annals of Human Genetics|September 13, 2011
Age-related penetrance of hereditary atypical hemolytic uremic syndromeMaren Sullivan, Lisa A Rybicki, Aurelia Winter, et al.
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.
Neuroendocrinology|March 21, 2015
Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed TomographyIlona Michałowska, Jarosław B Ćwikła, Mariola Pęczkowska, et al.
Pageof 12