H P Neumann
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Explore the profile of H P Neumann including associated specialties, affiliations and a list of published articles.
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112
Citations
1771
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Recent Articles
1.
Groeben H, Nottebaum B, Alesina P, Traut A, Neumann H, Walz M
Br J Anaesth
. 2017 Jan;
118(2):182-189.
PMID: 28100521
Background: Mortality associated with surgery for phaeochromocytoma has dramatically decreased over the last decades. Many factors contributed to the dramatic decline of the mortality rate, and the influence of an...
2.
Jilg C, Neumann H, Glasker S, Schafer O, Ardelt P, Schwardt M, et al.
Urol Int
. 2011 Dec;
88(1):71-8.
PMID: 22156657
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...
3.
Kreusel K, Krause L, Graul-Neumann L, Bechrakis N, Neumann H, Foerster M
Klin Monbl Augenheilkd
. 2009 Nov;
226(11):939-43.
PMID: 19916152
Background: The aim of this study was to characterise the results of a screening for von Hippel-Lindau disease (VHL), angiomatosis retinae (AR) and further VHL lesions in at-risk relatives of...
4.
Cybulla M, Walter K, Neumann H, Widmer U, Scharer M, Sunder-Plassmann G, et al.
Dtsch Med Wochenschr
. 2007 Jul;
132(28-29):1505-9.
PMID: 17607649
Background And Objective: Fabry's disease is a rare, X-chromosome linked recessive lysosomal storage disorder. In its course multiple organ damage occurs, e.g. in skin, nerves, kidneys and heart. The disease...
5.
Boedeker C, Ridder G, Neumann H, Maier W, Schipper J
Laryngorhinootologie
. 2004 Sep;
83(9):585-92.
PMID: 15372340
Background: Paragangliomas of the head and neck represent rare tumors of neural crest origin that arise from chemoreceptors. They are highly vascular neoplasms that are benign in the majority of...
6.
Gimm O, Koch C, Januszewicz A, Opocher G, Neumann H
Front Horm Res
. 2003 Dec;
31:45-60.
PMID: 14674304
Until very recently, the majority of hereditary pheochromocytomas were related to the MEN 2 and the VHL. In rare instances, hereditary pheochromocytoma was reported in patients with NF1. In addition,...
7.
Astuti D, Agathanggelou A, Honorio S, Dallol A, Martinsson T, Kogner P, et al.
Oncogene
. 2001 Dec;
20(51):7573-7.
PMID: 11709729
Deletions of chromosome 3p are frequent in many types of neoplasia including neural crest tumours such as neuroblastoma (NB) and phaeochromocytoma. Recently we isolated several candidate tumour suppressor genes (TSGs)...
8.
Neumann H, Riegler P, Huber W, Corradini R, Sessa A, Fontana D, et al.
Contrib Nephrol
. 2001 Nov;
(136):193-207.
PMID: 11688380
No abstract available.
9.
Neumann H, Reincke M, Eng C
N Engl J Med
. 2001 Aug;
345(7):547-8.
PMID: 11519521
No abstract available.
10.
Bender B, Eng C, Olschewski M, Berger D, Laubenberger J, Altehofer C, et al.
J Med Genet
. 2001 Aug;
38(8):508-14.
PMID: 11483638
Background: Germline mutations of the VHL gene cause von Hippel-Lindau syndrome (VHL). In southern Germany, a specific mutation in this gene, c.505 T>C, is one of the most frequent alterations...