Zobrazeno 1 - 10
of 13
pro vyhledávání: '"B U, Bender"'
Publikováno v:
Praxis. 92:450-453
Die mikroskopische Polyangiitis (MPA) ist eine seltene Vaskulitis, welche definiert ist als Kleingefässvaskulitis ohne Granulombildung mit immunhistochemisch weitgehend fehlenden Immunkomplexablagerungen. Die MPA betrifft beide Geschlechter gleich h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::644d8e586b14b00fb5438f3093241320
https://doi.org/10.1024/0369-8394.92.10.450
https://doi.org/10.1024/0369-8394.92.10.450
Autor:
B. U. Bender, Hartmut P. H. Neumann
Publikováno v:
Journal of Internal Medicine. 243:541-545
A total of 146 intragenic germline mutations of the von Hippel-Lindau (VHL) gene are known and this figure is still increasing. To date, information for mutation-specific genetic counselling is insufficient, since either the total number of carriers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea809b01379588666234118794d1febe
https://doi.org/10.1046/j.1365-2796.1998.00336.x
https://doi.org/10.1046/j.1365-2796.1998.00336.x
Autor:
B. U. Bender
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 82:3356-3360
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b770109d132e993e683b7018ac683f53
https://doi.org/10.1210/jc.82.10.3356
https://doi.org/10.1210/jc.82.10.3356
Autor:
G. Frankc, R. Munk, Hartmut P. H. Neumann, T. W. Apel, B. U. Bender, Sarah R. McWhinney, Charis Eng, M. Maier-Woelfle, W. M. Smith, C. Altehoefer, A. Klein-Franke, Andrzej Januszewicz, M. Reineke, M. K. WaIz, M. Brauckhoff, Mariola Pęczkowska, S. Glaesker, J. Schipper, Oliver Gimm, C. Szmigielski, K. Zerres, C. Hoang-Vu, Birke Bausch, P. Klose, H. Schmidt, T. Manz, Massimo Mannelli, M. Treier, J. Klisch
Publikováno v:
L'Endocrinologo. 4:40-42
Premessa Il gruppo dei geni che predispongono al feocromocitoma, che include il proto-oncogene RET [associato alla neoplasia endocrina multipla tipo 2 (MEN-2)] e il gene onco-soppressore VHL (associato con la malattia di von Hippel-Lindau) comprende
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f602d09d9ce99f289070749d93e2abc2
https://doi.org/10.1007/bf03344445
https://doi.org/10.1007/bf03344445
Autor:
G. Franke, J. Schipper, H. P. H. Neumann, Oliver Gimm, B. Bausch, J. Klisch, C. Altehoefer, K. Zerres, Charis Eng, Andrzej Januszewicz, B. U. Bender, S. R. McWhinney
Publikováno v:
Hormone and Metabolic Research. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcc58d84245f4ae5ae8e378e3a3ffee6
https://doi.org/10.1055/s-2004-830835
https://doi.org/10.1055/s-2004-830835
Publikováno v:
Praxis. 92(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1366ad7235094a998942c9e795fed842
https://pubmed.ncbi.nlm.nih.gov/12674588
https://pubmed.ncbi.nlm.nih.gov/12674588
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(12)
Pheochromocytomas arise sporadically and as a component tumor of the inherited cancer syndromes von Hippel-Lindau disease (VHL), multiple endocrine neoplasia type 2 (MEN 2), and type 1 neurofibromatosis. Germline mutations of the VHL tumor suppressor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b8e4cd07356e691da65144f53a769dc
https://pubmed.ncbi.nlm.nih.gov/11134110
https://pubmed.ncbi.nlm.nih.gov/11134110
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(8)
Familial pheochromocytoma, increasingly diagnosed in asymptomatic subjects with inherited syndromes such as multiple endocrine neoplasia type 2 and Von Hippel-Lindau disease, is frequently bilateral and multifocal, but very rarely malignant. Therefor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14e18f4fdf3e53231f082374650faafd
https://pubmed.ncbi.nlm.nih.gov/10443647
https://pubmed.ncbi.nlm.nih.gov/10443647
Publikováno v:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 96(2)
Capillary retinal angiomas are rare vascular tumors that frequently occur in von Hippel-Lindau syndrome (vHL) but may also be sporadic. In all patients presenting with this tumor a thorough search for other vHL-associated lesions must be performed. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0d12f4f50ac810cfa8eb0b7606071eb4
https://pubmed.ncbi.nlm.nih.gov/10095351
https://pubmed.ncbi.nlm.nih.gov/10095351
Autor:
H P, Neumann, B U, Bender, D P, Berger, J, Laubenberger, W, Schultze-Seemann, U, Wetterauer, F J, Ferstl, E W, Herbst, G, Schwarzkopf, F J, Hes, C J, Lips, J M, Lamiell, O, Masek, P, Riegler, B, Mueller, D, Glavac, H, Brauch
Publikováno v:
The Journal of urology. 160(4)
Renal cell carcinoma occurs as a sporadic tumor but may be part of the autosomal dominant von Hippel-Lindau disease, characterized by retinal and central nervous system hemangioblastoma, pheochromocytoma, pancreatic cysts and renal cell carcinoma. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce4a3077b0767d5843eec5f3852a6088
https://pubmed.ncbi.nlm.nih.gov/9751329
https://pubmed.ncbi.nlm.nih.gov/9751329