Published in N Engl J Med on October 14, 2010
Adverse ophthalmic reaction in poppers users: case series of 'poppers maculopathy'. Eye (Lond) (2012) 1.28
Is the mechanism of 'poppers maculopathy' photic injury? Eye (Lond) (2013) 1.03
'Poppers maculopathy'--an emerging ophthalmic reaction to recreational substance abuse. Eye (Lond) (2012) 0.87
MRI findings of elevated intracranial pressure in cerebral venous thrombosis versus idiopathic intracranial hypertension with transverse sinus stenosis. Neuroophthalmology (2013) 0.81
Ocular manifestations of drug and alcohol abuse. Curr Opin Ophthalmol (2013) 0.75
Flash photography-induced maculopathy. GMS Ophthalmol Cases (2011) 0.75
Poppers maculopathy or retinopathy? Eye (Lond) (2014) 0.75
Multimodal imaging of foveal cavitation in retinal dystrophies. Graefes Arch Clin Exp Ophthalmol (2016) 0.75
[Bilateral central scotoma in a 28-year-old patient with CADASIL syndrome]. Ophthalmologe (2016) 0.75
Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa. Science (2010) 3.92
Seven new loci associated with age-related macular degeneration. Nat Genet (2013) 3.81
Interim results from the international trial of Second Sight's visual prosthesis. Ophthalmology (2012) 3.35
Identification and characterization of rod-derived cone viability factor. Nat Genet (2004) 2.63
Using spectral-domain optical coherence tomography imaging to identify the presence of retinal silicone oil emulsification after silicone oil tamponade. Retina (2013) 2.22
Role of hyaluronidase in diplopia after peribulbar anesthesia for cataract surgery. Ophthalmology (2005) 2.10
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2009) 1.93
NMNAT1 mutations cause Leber congenital amaurosis. Nat Genet (2012) 1.86
Panretinal, high-resolution color photography of the mouse fundus. Invest Ophthalmol Vis Sci (2007) 1.82
Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet J Rare Dis (2012) 1.79
Persistence of fundus fluorescence after use of indocyanine green for macular surgery. Ophthalmology (2003) 1.73
Characterization of macular edema from various etiologies by optical coherence tomography. Am J Ophthalmol (2005) 1.71
Topography of patchy retinal whitening during acute perfused retinal vein occlusion by optical coherence tomography and adaptive optics fundus imaging. Eur J Ophthalmol (2011) 1.60
High resolution fundus imaging by confocal scanning laser ophthalmoscopy in the mouse. Vision Res (2005) 1.59
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet J Rare Dis (2011) 1.57
Foveal damage in habitual poppers users. Arch Ophthalmol (2011) 1.56
Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa. Mol Ther (2009) 1.53
Inherited retinal degenerations: therapeutic prospects. Biol Cell (2004) 1.44
CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice. EMBO Mol Med (2013) 1.42
En Face OCT Imaging for the Diagnosis of Outer Retinal Tubulations in Age-Related Macular Degeneration. J Ophthalmol (2012) 1.39
EYS is a major gene for rod-cone dystrophies in France. Hum Mutat (2010) 1.39
Optical coherence tomography findings in tamoxifen retinopathy. Am J Ophthalmol (2005) 1.36
CRB1 mutations in inherited retinal dystrophies. Hum Mutat (2011) 1.34
Foveal shape and structure in a normal population. Invest Ophthalmol Vis Sci (2011) 1.32
Novel COL4A1 mutations associated with HANAC syndrome: a role for the triple helical CB3[IV] domain. Am J Med Genet A (2010) 1.31
Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa. Hum Mutat (2010) 1.26
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2012) 1.25
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families. Invest Ophthalmol Vis Sci (2005) 1.25
Anxiety and depression prevalence rates in age-related macular degeneration. Invest Ophthalmol Vis Sci (2007) 1.25
Rod-derived cone viability factor for treating blinding diseases: from clinic to redox signaling. Sci Transl Med (2010) 1.20
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2012) 1.18
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. Hum Mol Genet (2012) 1.18
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. J Cell Biol (2012) 1.16
Retinal degenerations: from cell signaling to cell therapy; pre-clinical and clinical issues. Curr Gene Ther (2007) 1.15
The glutamate transporter EAAT5 works as a presynaptic receptor in mouse rod bipolar cells. J Physiol (2006) 1.15
Retinal inner nuclear layer microcystic changes in optic nerve atrophy: a novel spectral-domain OCT finding. Retina (2013) 1.11
Surgical management of epiretinal membrane in young patients. Am J Ophthalmol (2002) 1.11
Genotyping microarray for CSNB-associated genes. Invest Ophthalmol Vis Sci (2009) 1.10
Adaptive optics imaging of geographic atrophy. Invest Ophthalmol Vis Sci (2013) 1.07
In vivo anterior segment imaging in the rat eye with high speed white light full-field optical coherence tomography. Opt Express (2005) 1.07
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness. Am J Hum Genet (2010) 1.05
Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients. Invest Ophthalmol Vis Sci (2010) 1.05
Retinitis pigmentosa and other dystrophies. Dev Ophthalmol (2010) 1.03
Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports. BMC Med Genet (2010) 1.03
Retinal-cell-conditioned medium prevents TNF-alpha-induced apoptosis of purified ganglion cells. Invest Ophthalmol Vis Sci (2005) 1.02
Evidence for glutamate-mediated excitotoxic mechanisms during photoreceptor degeneration in the rd1 mouse retina. Mol Vis (2005) 1.01
Copy-number variations in EYS: a significant event in the appearance of arRP. Invest Ophthalmol Vis Sci (2011) 1.01
The aging of the retina. Exp Gerontol (2003) 1.01
Evaluation of retinal function and flicker light-induced retinal vascular response in normotensive patients with diabetes without retinopathy. Invest Ophthalmol Vis Sci (2011) 1.00
Ocular tissue imaging using ultrahigh-resolution, full-field optical coherence tomography. Invest Ophthalmol Vis Sci (2004) 0.99
A low-cost and simple imaging technique of the anterior and posterior segments: eye fundus, ciliary bodies, iridocorneal angle. Invest Ophthalmol Vis Sci (2008) 0.98
The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina. Hum Mol Genet (2009) 0.97
Retinal vein occlusions. Dev Ophthalmol (2010) 0.97
Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations. J Inherit Metab Dis (2010) 0.97
The extended clinical phenotype of dome-shaped macula. Graefes Arch Clin Exp Ophthalmol (2014) 0.96
Mutations in IMPG1 cause vitelliform macular dystrophies. Am J Hum Genet (2013) 0.96
Partial characterization of retina-derived cone neuroprotection in two culture models of photoreceptor degeneration. Invest Ophthalmol Vis Sci (2003) 0.95
In vivo observation of the locomotion of microglial cells in the retina. Glia (2010) 0.94
Erythrocyte and leukocyte dynamics in the retinal capillaries of diabetic mice. Exp Eye Res (2003) 0.94
Lack of Niemann-Pick type C1 induces age-related degeneration in the mouse retina. Mol Cell Neurosci (2009) 0.94
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits. Rejuvenation Res (2007) 0.94
Functional and high resolution retinal imaging assessment in a case of ocular siderosis. Doc Ophthalmol (2013) 0.94
The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes. Biochim Biophys Acta (2008) 0.94
Disease-causing mutations in BEST1 gene are associated with altered sorting of bestrophin-1 protein. Int J Mol Sci (2013) 0.94
Morphometric analysis of small arteries in the human retina using adaptive optics imaging: relationship with blood pressure and focal vascular changes. J Hypertens (2014) 0.92
Involvement of Pleiotrophin in CNTF-mediated differentiation of the late retinal progenitor cells. Dev Biol (2006) 0.92
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy. J Neurol Neurosurg Psychiatry (2010) 0.91
AAV-mediated gene delivery in Dp71-null mouse model with compromised barriers. Glia (2013) 0.90
RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlation. Hum Mutat (2011) 0.90
Association between visual acuity and medical and non-medical costs in patients with wet age-related macular degeneration in France, Germany and Italy. Drugs Aging (2008) 0.90
A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family. Mol Vis (2011) 0.90
Subretinal lymphomatous infiltration in primary intraocular lymphoma revealed by optical coherence tomography. Graefes Arch Clin Exp Ophthalmol (2011) 0.89
mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein. RNA (2006) 0.89
Differential proteomic analysis of the mouse retina: the induction of crystallin proteins by retinal degeneration in the rd1 mouse. Mol Cell Proteomics (2003) 0.89
Microvascular remodeling after occlusion-recanalization of a branch retinal vein in rats. Invest Ophthalmol Vis Sci (2004) 0.89
Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death. PLoS One (2011) 0.88
The cost-effectiveness of the Argus II retinal prosthesis in Retinitis Pigmentosa patients. BMC Ophthalmol (2014) 0.87
Combined central retinal arterial and venous obstruction: emergency ophthalmic arterial fibrinolysis. Radiology (2002) 0.87
Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort. Hum Mutat (2011) 0.87
PromAn: an integrated knowledge-based web server dedicated to promoter analysis. Nucleic Acids Res (2006) 0.87
Cellular localization of the vesicular inhibitory amino acid transporter in the mouse and human retina. J Comp Neurol (2002) 0.87
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management. Ophthalmic Epidemiol (2013) 0.86
Mammalian retinal horizontal cells are unconventional GABAergic neurons. J Neurochem (2010) 0.86
Human induced pluripotent stem cells as a tool to model a form of Leber congenital amaurosis. Cell Reprogram (2013) 0.86