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Hartmut P H Neumann

Showing results (21-30 of 132) with videos related to

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Seminars in Nephrology|March 14, 2002
How many pathways to pheochromocytoma?Hartmut P H Neumann, Stefan Hoegerle, Tanja Manz, et al.
The Journal of Urology|September 17, 2004
Malignant pheochromocytoma associated with germline mutation of the SDHB geneZishan Allibhai, George Rodrigues, Ed Brecevic, et al.
Archives of Dermatology|December 17, 2003
Soft nodules at the tip of the tongue of a 26-year-old manMartin Leverkus, Hartmut P H Neumann, Eva-Bettina Brocker, et al.
Acta Ophthalmologica Scandinavica|June 5, 2003
A sporadic case of von Hippel-Lindau disease with a secondary maculopathy as the presenting signKlaus-Martin Kreusel, Nikolaos E Bechrakis, Hartmut P H Neumann, et al.
American Journal of Ophthalmology|February 24, 2006
Pars plana vitrectomy for juxtapapillary capillary retinal angiomaKlaus-Martin Kreusel, Nikolaos E Bechrakis, Hartmut P H Neumann, et al.
The Lancet. Diabetes & Endocrinology|November 29, 2020
Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literatureIrina Bancos, Elizabeth Atkinson, Charis Eng, et al.
Clinical Nuclear Medicine|January 10, 2012
Is there an optimal scan time for 6-[F-18]fluoro-L-DOPA PET in pheochromocytomas and paragangliomas?Michael Hentschel, Christof Rottenburger, Carsten C Boedeker, et al.
European Urology|April 14, 2005
Laparoscopic adrenal surgery for recurrent tumours in patients with hereditary phaeochromocytomaThiagarajan Nambirajan, Karl Leeb, Hartmut P H Neumann, et al.
Clinical Chemistry and Laboratory Medicine|April 19, 2007
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiencyBernhard U Bender, Thomas Quaschning, Hartmut P H Neumann, et al.
Neurosurgery|February 25, 2011
Doppler-sonographically guided resection of central nervous system hemangioblastomasSven Gläsker, Mukesch J Shah, Beate Hippchen, et al.
Pageof 14

Showing results (21-30 of 132) with videos related to

Sort By:
Pageof 14
Seminars in Nephrology|March 14, 2002
How many pathways to pheochromocytoma?Hartmut P H Neumann, Stefan Hoegerle, Tanja Manz, et al.
The Journal of Urology|September 17, 2004
Malignant pheochromocytoma associated with germline mutation of the SDHB geneZishan Allibhai, George Rodrigues, Ed Brecevic, et al.
Archives of Dermatology|December 17, 2003
Soft nodules at the tip of the tongue of a 26-year-old manMartin Leverkus, Hartmut P H Neumann, Eva-Bettina Brocker, et al.
Acta Ophthalmologica Scandinavica|June 5, 2003
A sporadic case of von Hippel-Lindau disease with a secondary maculopathy as the presenting signKlaus-Martin Kreusel, Nikolaos E Bechrakis, Hartmut P H Neumann, et al.
American Journal of Ophthalmology|February 24, 2006
Pars plana vitrectomy for juxtapapillary capillary retinal angiomaKlaus-Martin Kreusel, Nikolaos E Bechrakis, Hartmut P H Neumann, et al.
The Lancet. Diabetes & Endocrinology|November 29, 2020
Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literatureIrina Bancos, Elizabeth Atkinson, Charis Eng, et al.
Clinical Nuclear Medicine|January 10, 2012
Is there an optimal scan time for 6-[F-18]fluoro-L-DOPA PET in pheochromocytomas and paragangliomas?Michael Hentschel, Christof Rottenburger, Carsten C Boedeker, et al.
European Urology|April 14, 2005
Laparoscopic adrenal surgery for recurrent tumours in patients with hereditary phaeochromocytomaThiagarajan Nambirajan, Karl Leeb, Hartmut P H Neumann, et al.
Clinical Chemistry and Laboratory Medicine|April 19, 2007
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiencyBernhard U Bender, Thomas Quaschning, Hartmut P H Neumann, et al.
Neurosurgery|February 25, 2011
Doppler-sonographically guided resection of central nervous system hemangioblastomasSven Gläsker, Mukesch J Shah, Beate Hippchen, et al.
Pageof 14