Photodynamic therapy in symptomatic parafoveal  telangiectasia secondary to Osler−Rendu−Weber disease-Reference-Cited by-同舟云学术

Photodynamic therapy in symptomatic parafoveal  telangiectasia secondary to Osler−Rendu−Weber disease

Published:2005-07-26 Issue:2 Volume:84 Page:273-275
ISSN:1395-3907
Container-title:Acta Ophthalmologica Scandinavica
language:en
Short-container-title:

Author:

Mennel Stefan,Hoerle Steffen,Meyer Carsten H.

Publisher

Wiley

Subject

Ophthalmology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0420.2005.00519.x/fullpdf

Reference6 articles.

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2. Defective paracrine signalling by TGF-ß in yolk sac vasculature of endoglin mutant mice: a paradigm for hereditary haemorrhagic telangiectasia;Carvalho;Development,2004

3. Intraoperative choroidal haemorrhage in the Osler-Rendu-Weber syndrome;Mahmoud;Am J Ophthalmol,2002

4. Endoglin, a TGF-ß binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1;McAllister;Nat Genet,1994

5. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes;Osler;Bull Johns Hopkins Hosp,1901

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