Peter Charbel Issa
Peter Charbel Issa
Oxford Eye Hosptial, University of Oxford
oxon.org üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress
D Weismann, K Hartvigsen, N Lauer, KL Bennett, HPN Scholl, ...
Nature 478 (7367), 76-81, 2011
4312011
Systemic complement activation in age-related macular degeneration
HPN Scholl, P Charbel Issa, M Walier, S Janzer, B Pollok-Kopp, ...
PLoS One 3 (7), e2593, 2008
3542008
High-resolution spectral domain-OCT imaging in geographic atrophy associated with age-related macular degeneration
M Fleckenstein, P Charbel Issa, HM Helb, S Schmitz-Valckenberg, ...
Investigative ophthalmology & visual science 49 (9), 4137-4144, 2008
2582008
Macular Telangiectasia Type 2
P Charbel Issa, MC Gillies, EY Chew, AC Bird, T Heeren, T Peto, FG Holz, ...
Progress in Retinal and Eye Research 34, 49-77, 2013
2242013
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
I Ebermann, HPN Scholl, P Charbel Issa, E Becirovic, J Lamprecht, ...
Human genetics 121 (2), 203-211, 2007
2202007
Reversal of end-stage retinal degeneration and restoration of visual function by photoreceptor transplantation
MS Singh, P Charbel Issa, R Butler, C Martin, DM Lipinski, S Sekaran, ...
Proceedings of the National Academy of Sciences 110 (3), 1101-1106, 2013
2072013
Pseudoxanthoma elasticum: genetics, clinical manifestations and therapeutic approaches
RP Finger, P Charbel Issa, MS Ladewig, C Götting, C Szliska, HPN Scholl, ...
Survey of ophthalmology 54 (2), 272-285, 2009
1932009
An update on the genetics of age-related macular degeneration
HPN Scholl, M Fleckenstein, P Charbel Issa, C Keilhauer, FG Holz, ...
Molecular vision 13, 196-205, 2007
189*2007
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies
T Eisenberger, C Neuhaus, AO Khan, C Decker, MN Preising, ...
PloS one 8 (11), e78496, 2013
1712013
Genetic control of the alternative pathway of complement in humans and age-related macular degeneration
LA Hecker, AO Edwards, E Ryu, N Tosakulwong, KH Baratz, WL Brown, ...
Human molecular genetics 19 (1), 209-215, 2010
1432010
Clinical evaluation of simultaneous confocal scanning laser ophthalmoscopy imaging combined with high‐resolution, spectral‐domain optical coherence tomography
HM Helb, P Charbel Issa, M Fleckenstein, S Schmitz‐Valckenberg, ...
Acta Ophthalmologica 88 (8), 842-849, 2010
1292010
Abnormal macular pigment distribution in type 2 idiopathic macular telangiectasia
HM Helb, P Charbel Issa, RLP van der Veen, TTJM Berendschot, ...
Retina 28 (6), 808-816, 2008
1172008
Confocal blue reflectance imaging in type 2 idiopathic macular telangiectasia
P Charbel Issa, TTJM Berendschot, G Staurenghi, FG Holz, HPN Scholl
Investigative ophthalmology & visual science 49 (3), 1172-1177, 2008
1112008
The significance of the complement system for the pathogenesis of age-related macular degeneration—current evidence and translation into clinical application
P Charbel Issa, NV Chong, HPN Scholl
Graefe's Archive for Clinical and Experimental Ophthalmology 249 (2), 163-174, 2011
1052011
Microperimetric assessment of patients with type 2 idiopathic macular telangiectasia
P Charbel Issa, HM Helb, K Rohrschneider, FG Holz, HPN Scholl
Investigative ophthalmology & visual science 48 (8), 3788-3795, 2007
1012007
Findings in fluorescein angiography and optical coherence tomography after intravitreal bevacizumab in type 2 idiopathic macular telangiectasia
P Charbel Issa, FG Holz, HPN Scholl
Ophthalmology 114, 1736-1742, 2007
1012007
Tracking progression with spectral-domain optical coherence tomography in geographic atrophy caused by age-related macular degeneration
M Fleckenstein, S Schmitz-Valckenberg, C Adrion, I Krämer, N Eter, ...
Investigative ophthalmology & visual science 51 (8), 3846-3852, 2010
992010
Reading performance is reduced by parafoveal scotomas in patients with macular telangiectasia type 2
RP Finger, P Charbel Issa, R Fimmers, FG Holz, GS Rubin, HPN Scholl
Investigative ophthalmology & visual science 50 (3), 1366-1370, 2009
962009
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction
I Ebermann, M Walger, HPN Scholl, P Charbel Issa, C Lüke, G Nürnberg, ...
Human mutation 28 (6), 571-577, 2007
962007
Quantification of reduced macular pigment optical density in the central retina in macular telangiectasia type 2
P Charbel Issa, RLP van der Veen, A Stijfs, FG Holz, HPN Scholl, ...
Experimental eye research 89 (1), 25-31, 2009
932009
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20