Doyne’s Honeycomb Dystrophy
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-35951-4_999-1
Reference5 articles.
1. Brown J, Webster Arm Sheffield VC, Stone EM (2006) Molecular genetics of retinal disease. In: Ryan S (ed-in-chief), Schachat AP (ed) Retina, 4th edn. Elsevier Mosby, St Louis, pp 392–395
2. Haimovici R, Wroblewski J, Piguet B, Fitzke FW, Holder GE, Arden GB, Bird AC (2002) Symptomatic abnormalities of dark adapation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy). Eye 16:7–15
3. Lenassi E, Troeger E, Wilke R, Tufail A, Hawlina M, Jeffery G, Webster AR (2013) Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1). Am J Ophthalmol 155(1):190–198
4. Sohn EH, Patel PJ, MacLaren RE, Adatia FA, Pal B, Webster Arm Tufail A (2011) Responsiveness of choroidal neovascular membranes in patients with R345Wmutation in fibulin 3 (Doyne honeycomb retinal dystrophy) to anti-vascular endothelial growth factor therapy. Arch Ophthalmol 129(12):1226–1228
5. Stone EM, Lotery AJ, Munier FL, Heon E, Piguet B, Guymer RH, Vandenburgh K, Cousin P, Nishimura D, Swidereski RE, Silvestri G, Mackey DA, Hageman GS, Bird AC, Sheffield VC, Schoderet D (1999) A single EFEMP1 mutation associated with both Malattia Leventenes and Doyne Honeycomb retinal dystrophy. Nat Genet 22:199–202
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