Von-Hippel-Lindau-Erkrankung

Author:

Neumann H. P. H.,Cybulla M.,Gläsker S.,Coulin C.,Van Velthoven V.,Berlis A.,Hader C.,Schäfer O.,Treier M.,Brink I.,Schultze-Seemann W.,Leiber C.,Rückauer K.,Junker B.,Agostini F. J.,Hetzel A.,Boedeker C. C.

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference29 articles.

1. Bausch B, Boedeker CC, Berlis A et al (2006) Genetic and Clinical Investigation of Pheochromocytoma: A 22-year experience, from Freiburg, Germany to International Effort. Ann New York Acad Sciences 1073: 112–137

2. Bausch B, Borozdin W, Neumann HPH et al (2006) Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma. N Engl J Med 354: 2729–2731

3. Böhlin T, Plate KH, Haltia M et al (2000) Von Hippel-Lindau disease and capillary haemangioblastoma. In: Kleihues P, Cawenee WK (eds) Pathology and Genetics of Tumours of the Nervous System. World Health Organization, Lyon, pp 223–226

4. Brauch H, Kishida T, Glavac D et al (1995) Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect. Hum Genet 95: 551–556

5. Collins ET (1894) Intra-ocular growths. Two cases, brother and sister, with peculiar vascular new growth, probably primarily retinal, affecting both eyes. Transact Ophtalmol Soc U K 14: 141–149

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