Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hartmut Ph Neumann"'
Autor:
Christian Offergeld, Christoph Brase, Svetlana Yaremchuk, Irina Mader, Hans Christian Rischke, Sven Gläsker, Kurt W Schmid, Thorsten Wiech, Simon F Preuss, Carlos Suárez, Tomasz Kopć, Attila Patocs, Nelson Wohllk, Mahdi Malekpour, Carsten C Boedeker, Hartmut PH Neumann
Publikováno v:
Clinics, Vol 67, Pp 19-28 (2012)
Head and neck paragangliomas are tumors arising from specialized neural crest cells. Prominent locations are the carotid body along with the vagal, jugular, and tympanic glomus. Head and neck paragangliomas are slowly growing tumors, with some caroti
Externí odkaz:
https://doaj.org/article/615823b91ca145aea7e52762902a7e02
Autor:
Cordula A. Jilg, Wolfgang Schultze-Seemann, Sven Gläsker, P. U. Ardelt, Hartmut Ph Neumann, O. Schäfer, M. Schwardt
Publikováno v:
Urologia Internationalis. 88:71-78
Objective: To evaluate the growth kinetics of renal cell carcinoma (RCC) in von Hippel-Lindau (VHL) disease in a large trial by CT/MRI scan. VHL disease is a multisystemic disorder predisposing to renal cysts and cancer. There is a general assumption
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38093c77d12a06d12ede0a135269df08
https://doi.org/10.1159/000333348
https://doi.org/10.1159/000333348
Autor:
Claudia Hader, Sven Gläsker, Jan-Helge Klingler, K. Müller, C. Würtenberger, Vera Van Velthoven, Josef Zentner, Hartmut Ph Neumann
Publikováno v:
Central European Neurosurgery. 71:80-87
Hemangioblastomas are rare CNS tumors, which are mostly located in the posterior fossa or spinal cord and occasionally in spinal nerves. They can occur sporadically or as a component tumor of von Hippel-Lindau (VHL) disease, an autosomal dominant tum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb55014a9e733177c62e043e57b7d72d
https://doi.org/10.1055/s-0029-1234040
https://doi.org/10.1055/s-0029-1234040
Publikováno v:
Neurosurgery. 68(2 Suppl)
BACKGROUND: Central nervous system (CNS) hemangioblastomas are a benign condition, which can be permanently cured by complete surgical removal. However, the vascular nature of these lesions and difficulties in localizing the tumors account for operat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df1bbeaa7517b24f1072e4ec3b61d4d
https://pubmed.ncbi.nlm.nih.gov/21346656
https://pubmed.ncbi.nlm.nih.gov/21346656
Autor:
Ingo Brink, Andreas Hetzel, Bernd Junker, Markus Cybulla, Hartmut Ph Neumann, Sven Gläsker, Wolfgang Schultze-Seemann, Ansgar Berlis, Carsten Christof Boedeker, Vera Van Velthoven, K. Rückauer, C. Coulin, F. J. Agostini, C. Leiber, O. Schäfer, M. Treier, Claudia Hader
Das Von-Hippel-Lindau-Syndrom ist eine hereditare Tumorerkrankung. Die interdisziplinare Versorgung der Patienten ist von zentraler Bedeutung, weil die Erkrankung nicht nur die Augen, sondern zahlreiche weitere Zielorgane betrifft. Klassische Verande
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4a3a8986ac501aa2729f83cf330e41e
https://opus.bibliothek.uni-augsburg.de/opus4/files/91298/91298.pdf
https://opus.bibliothek.uni-augsburg.de/opus4/files/91298/91298.pdf
