von Hippel-Lindau disease: treatment of retinal haemangioblastomas by targeted therapy with systemic bevacizumab
Author:
Publisher
Wiley
Subject
Ophthalmology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1755-3768.2009.01611.x/fullpdf
Reference6 articles.
1. Rapid and durable recovery of visual function in a patient with von hippel-lindau syndrome after systemic therapy with vascular endothelial growth factor receptor inhibitor su5416;Aiello;Ophthalmology,2002
2. Systemic bevacizumab treatment of a juxtapapillary retinal haemangioma;Von Buelow;Acta Ophthalmol Scand,2007
3. Treatment of von Hippel-Lindau retinal hemangioblastoma by the vascular endothelial growth factor receptor inhibitor SU5416 is more effective for associated macular edema than for hemangioblastomas;Girmens;Am J Ophthalmol,2003
4. Combined intravitreal anti-vascular endothelial growth factor (Avastin) and photodynamic therapy to treat retinal juxtapapillary capillary haemangioma;Mennel;Acta Ophthalmol,2009
5. von Hippel-Lindau disease;Singh;Surv Ophthalmol,2001
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