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ArticlesPeer ReviewedFull Text
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome
Author / Creator:Manuelian, T ; Hellwage, J ; Meri, S ; Caprioli, J ; Noris, M ; Heinen, S ; Jozsi, M ; Neumann, HPH ; Remuzzi, G ; Zipfel, P F
Publisher:American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2003-04, Vol.111 (8), p.1181-1190
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Germ-Line Mutations in Nonsyndromic Pheochromocytoma
Author / Creator:Neumann, Hartmut P.H ; Bausch, Birke ; McWhinney, Sarah R ; Bender, Bernhard U ; Gimm, Oliver ; Franke, Gerlind ; Schipper, Joerg ; Klisch, Joachim ; Altehoefer, Carsten ; Zerres, Klaus ; Januszewicz, Andrzej ; Smith, Wendy M ; Munk, Robin ; Manz, Tanja ; Glaesker, Sven ; Apel, Thomas W ; Treier, Markus ; Reineke, Martin ; Walz, Martin K ; Hoang-Vu, Cuong ; Brauckhoff, Michael ; Klein-Franke, Andreas ; Klose, Peter ; Schmidt, Heinrich ; Maier-Woelfle, Margarete ; Peçzkowska, Mariola ; Szmigielski, Cesary ; Eng, Charis
Publisher:Boston, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2002-05, Vol.346 (19), p.1459-1466
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Laparoscopic and Retroperitoneoscopic Treatment of Pheochromocytomas and Retroperitoneal Paragangliomas: Results of 161 Tumors in 126 Patients
Author / Creator:Walz, Martin K. ; Alesina, Piero F. ; Wenger, Frank A. ; Koch, J. Albrecht ; Neumann, Hartmut P. H. ; Petersenn, Stephan ; Schmid, Kurt W. ; Mann, Klaus
Publisher:New York: Springer‐Verlag
Journal title:World journal of surgery, 2006-05, Vol.30 (5), p.899-908
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Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries
Author / Creator:Neumann, H P H ; Salzmann, M ; Bohnert-Iwan, B ; Mannuelian, T ; Skerka, C ; Lenk, D ; Bender, B U ; Cybulla, M ; Riegler, P ; Königsrainer, A ; Neyer, U ; Bock, A ; Widmer, U ; Male, D A ; Franke, G ; Zipfel, P F
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2003-09, Vol.40 (9), p.676-681
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Novel mutations of the MET proto-oncogene in papillary renal carcinomas
Author / Creator:Schmidt, Laura ; Junker Kerstin ; Nakaigawa Noboru ; Kinjerski Tracy ; Weirich Gregor ; Miller, Maria ; Lubensky Irina ; Neumann, Hartmut PH ; Brauch Hiltrud ; Decker, Johann ; Vocke, Cathy ; Brown, James A ; Jenkins, Robert ; Richard, Stephane ; Bergerheim Ulf ; Gerrard, Bernard ; Dean, Michael ; Marston, Linehan W ; Zbar Berton
Publisher:New York: Nature Publishing Group
Journal title:Oncogene, 1999-04, Vol.18 (14), p.2343-2350
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Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas
Author / Creator:Kugelberg, Johan ; Welander, Jenny ; Schiavi, Francesca ; Fassina, Ambrogio ; Bäckdahl, Martin ; Larsson, Catharina ; Opocher, Giuseppe ; Söderkvist, Peter ; Dahia, Patricia L. ; Neumann, Hartmut P. H. ; Gimm, Oliver
Publisher:Boston: Springer US
Journal title:World journal of surgery, 2014-03, Vol.38 (3), p.724-732
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Endoscopic Treatment of Solitary, Bilateral, Multiple, and Recurrent Pheochromocytomas and Paragangliomas
Author / Creator:Walz, Martin K. ; Peitgen, Klaus ; Neumann, Hartmut P.H. ; Janssen, Onno E. ; Philipp, Thomas ; Mann, Klaus
Publisher:New York: Springer‐Verlag
Journal title:World journal of surgery, 2002-08, Vol.26 (8), p.1005-1012
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RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours
Author / Creator:Astuti, Dewi ; Agathanggelou, Angelo ; Honorio, Sofia ; Dallol, Ashraf ; Martinsson, Tommy ; Kogner, Per ; Cummins, Carole ; Neumann, Hartmut PH ; Voutilainen, Raimo ; Dahia, Patricia ; Eng, Charis ; Maher, Eamonn R ; Latif, Farida
Publisher:Basingstoke: Nature Publishing
Journal title:Oncogene, 2001-11, Vol.20 (51), p.7573-7577
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Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains
Author / Creator:Wolf, Matthias T.F. ; Mucha, Bettina E. ; Attanasio, Massimo ; Zalewski, Isabella ; Karle, Stephanie M. ; Neumann, Hartmut P.H. ; Rahman, Nazneen ; Bader, Birgit ; Baldamus, Conrad A. ; Otto, Edgar ; Witzgall, Ralph ; Fuchshuber, Arno ; Hildebrandt, Friedhelm
Publisher:New York, NY: Elsevier Inc
Journal title:Kidney international, 2003-11, Vol.64 (5), p.1580-1587
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Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma
Author / Creator:Astuti, D ; Morris, M ; Krona, C ; Abel, F ; Gentle, D ; Martinsson, T ; Kogner, P ; Neumann, H P H ; Voutilainen, R ; Eng, C ; Rustin, P ; Latif, F ; Maher, E R
Publisher:London: Nature Publishing Group UK
Journal title:British journal of cancer, 2004-11, Vol.91 (10), p.1835-1841
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Mutations of the SDHB and SDHD genes
Author / Creator:Pawlu, Christian ; Bausch, Birke ; Neumann, Hartmut P. H.
Publisher:Netherlands: Springer Nature B.V
Journal title:Familial cancer, 2005-01, Vol.4 (1), p.49-54
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Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome
Author / Creator:Lui, Weng Onn ; Chen, Jindong ; Glaesker, S ; Bender, BU ; Madura, C ; Khoo, Sok Kean ; Kort, E ; Larsson, C ; Neumann, HPH ; Teh, Bin Tean
Journal title:Oncogene, 2002-02, Vol.21 (7), p.1117-1122
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The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system
Author / Creator:Glasker, S. ; Bender, B. U ; Apel, T. W ; Natt, E. ; van Velthoven, V. ; Scheremet, R. ; Zentner, J. ; Neumann, H. P H
Publisher:London: BMJ
Journal title:Journal of neurology, neurosurgery and psychiatry, 1999-12, Vol.67 (6), p.758-762
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Subarachnoid haemorrhage due to cervical spinal cord haemangioblastomas in a patient with von Hippel-Lindau disease
Author / Creator:Berlis, A. ; Schumacher, M. ; Spreer, J. ; Neumann, H. P. H. ; van Velthoven, V.
Publisher:Austria: Springer Nature B.V
Journal title:Acta neurochirurgica, 2003-11, Vol.145 (11), p.1009-1013
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Dynamic contrast enhancement of paragangliomas of the head and neck: evaluation with time-resolved 2D MR projection angiography
Author / Creator:Arnold, Sebastian M. ; Strecker, Ralph ; Scheffler, Klaus ; Spreer, Joachim ; Schipper, Jörg ; Neumann, Hartmut P. H. ; Klisch, Joachim
Publisher:Germany: Springer Nature B.V
Journal title:European radiology, 2003-07, Vol.13 (7), p.1608-1611
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Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome
Author / Creator:Lui, Weng Onn ; Chen, Jindong ; Gläsker, Sven ; Bender, Bernhad U ; Madura, Casey ; Khoo, Sok Kean ; Kort, Eric ; Larsson, Catharina ; Neumann, Harmut PH ; Teh, Bin Tean
Publisher:Basingstoke: Nature Publishing
Journal title:Oncogene, 2002-02, Vol.21 (7), p.1117-1122
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VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality
Author / Creator:Bender, Bernhard U ; Eng, Charis ; Olschewski, Manfred ; Berger, Dietmar P ; Laubenberger, Jörg ; Altehöfer, Carsten ; Kirste, Günter ; Orszagh, Miro ; van Velthoven, Vera ; Miosczka, Henning ; Schmidt, Dieter ; Neumann, Hartmut P H
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2001-08, Vol.38 (8), p.508-514
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Case 13-2001: Genetic Testing in Pheochromocytoma
Author / Creator:Neumann, H P ; Reincke, M ; Eng, C
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2001-08, Vol.345 (7), p.547-548
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LBSAT62 Incidental Diagnosis Of Pheochromocytoma With Left Ventricle Hypertrophy And Bradycardia In A Normotensive Patient
Author / Creator:Eid, Mennaallah ; Zahra, Tasneem ; Vargas-Jerez, Julia
Publisher:Oxford: Oxford University Press
Journal title:Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A46-A47
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Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel-Lindau syndrome
Author / Creator:Kempermann, G ; Neumann, H P ; Scheremet, R ; Volk, B ; Mann, W ; Gilsbach, J ; Laszig, R
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 1996-09, Vol.61 (3), p.318-320
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Showing 1 to 20 of 27 results

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

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Germ-Line Mutations in Nonsyndromic Pheochromocytoma

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Laparoscopic and Retroperitoneoscopic Treatment of Pheochromocytomas and Retroperitoneal Paragangliomas: Results of 161 Tumors in 126 Patients

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Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

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Novel mutations of the MET proto-oncogene in papillary renal carcinomas

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Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas

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Endoscopic Treatment of Solitary, Bilateral, Multiple, and Recurrent Pheochromocytomas and Paragangliomas

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RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

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Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains

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Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma

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Mutations of the SDHB and SDHD genes

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Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome

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The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system

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Subarachnoid haemorrhage due to cervical spinal cord haemangioblastomas in a patient with von Hippel-Lindau disease

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Dynamic contrast enhancement of paragangliomas of the head and neck: evaluation with time-resolved 2D MR projection angiography

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Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome

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VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality

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Case 13-2001: Genetic Testing in Pheochromocytoma

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LBSAT62 Incidental Diagnosis Of Pheochromocytoma With Left Ventricle Hypertrophy And Bradycardia In A Normotensive Patient

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Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel-Lindau syndrome

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