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Hartmut P H Neumann

Showing results (11-20 of 132) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 23, 2006
Gross genomic rearrangement involving the TSC2-PKD1 contiguous deletion syndrome: characterization of the deletion event by quantitative polymerase chain reaction deletion assayDetlef Boehm, Janina Bacher, Hartmut P H Neumann
Current Opinion in Nephrology and Hypertension|October 18, 2003
Genetic screening in haemolytic uraemic syndromePeter F Zipfel, Hartmut P H Neumann, Mihály Józsi
The New England Journal of Medicine|November 7, 2019
Pheochromocytoma and Paraganglioma. ReplyHartmut P H Neumann, William F Young, Charis Eng
Human Molecular Genetics|October 15, 2020
Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicineRuth Casey, Hartmut P H Neumann, Eamonn R Maher
The New England Journal of Medicine|August 8, 2019
Pheochromocytoma and ParagangliomaHartmut P H Neumann, William F Young, Charis Eng
Onkologie|March 18, 2005
Von Hippel-Lindau disease--a rare disease important to recognizeMarkus Joerger, Dieter Koeberle, Hartmut P H Neumann, et al.
Clinical Nuclear Medicine|December 24, 2005
Fluorine-18 DOPA PET imaging of paraganglioma syndromeIngo Brink, Oliver Schaefer, Martin Walz, et al.
Journal of Hypertension|November 4, 2006
Pheochromocytoma: presentation, diagnosis and treatmentNicole Reisch, Mariola Peczkowska, Andrzej Januszewicz, et al.
Central European Journal of Urology|August 21, 2014
Diagnosis of extra-adrenal phaeochromocytoma after nephrectomyDimitri Barski, Samer Ezziddin, Sebastian Heikaus, et al.
Hormones & Cancer|May 11, 2012
Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytomaAlexander Weber, Michael M Hoffmann, Hartmut P H Neumann, et al.
Pageof 14

Showing results (11-20 of 132) with videos related to

Sort By:
Pageof 14
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 23, 2006
Gross genomic rearrangement involving the TSC2-PKD1 contiguous deletion syndrome: characterization of the deletion event by quantitative polymerase chain reaction deletion assayDetlef Boehm, Janina Bacher, Hartmut P H Neumann
Current Opinion in Nephrology and Hypertension|October 18, 2003
Genetic screening in haemolytic uraemic syndromePeter F Zipfel, Hartmut P H Neumann, Mihály Józsi
The New England Journal of Medicine|November 7, 2019
Pheochromocytoma and Paraganglioma. ReplyHartmut P H Neumann, William F Young, Charis Eng
Human Molecular Genetics|October 15, 2020
Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicineRuth Casey, Hartmut P H Neumann, Eamonn R Maher
The New England Journal of Medicine|August 8, 2019
Pheochromocytoma and ParagangliomaHartmut P H Neumann, William F Young, Charis Eng
Onkologie|March 18, 2005
Von Hippel-Lindau disease--a rare disease important to recognizeMarkus Joerger, Dieter Koeberle, Hartmut P H Neumann, et al.
Clinical Nuclear Medicine|December 24, 2005
Fluorine-18 DOPA PET imaging of paraganglioma syndromeIngo Brink, Oliver Schaefer, Martin Walz, et al.
Journal of Hypertension|November 4, 2006
Pheochromocytoma: presentation, diagnosis and treatmentNicole Reisch, Mariola Peczkowska, Andrzej Januszewicz, et al.
Central European Journal of Urology|August 21, 2014
Diagnosis of extra-adrenal phaeochromocytoma after nephrectomyDimitri Barski, Samer Ezziddin, Sebastian Heikaus, et al.
Hormones & Cancer|May 11, 2012
Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytomaAlexander Weber, Michael M Hoffmann, Hartmut P H Neumann, et al.
Pageof 14