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rdfs:label	11
skos:inScheme	http://hub.abes.fr/referentiel/bmjarticlecategories
is Subject of	Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature Different mutation of the XLRS1 gene causes juvenile retinoschisis with retinal white flecks Plasma homocysteine, methylene tetrahydrofolate reductase C677T and factor II G20210A polymorphisms, factor VIII, and VWF in central retinal vein occlusion Ocular involvement in congenital erythropoietic porphyria (Günther's disease): cytopathological evaluation of conjunctival and corneal changes Optic neuropathy and cerebellar ataxia associated with a rare missense variation (A14510G) of mitochondrial DNA Ophthalmic features of primary oxalosis after combined liver/kidney transplantation Ocular changes in heredo-oto-ophthalmo-encephalopathy Deletion in the OA1 gene in a family with congenital X linked nystagmus At what age could screening for familial retinoblastoma be stopped? A register based study 1945-98 Retinal dystrophies caused by mutations inRPE65: assessment of visual functions Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene Sorsby fundus dystrophy without a mutation in the TIMP-3 gene Prediction of prognosis in patients with uveal melanoma using fluorescence in situ hybridisation Pseudoexfoliation syndrome in Icelandic families Familial uveal melanoma: report on three sibling cases Report of a family with dominantly inherited upper lid entropion Genetic screening in a large family with juvenile onset primary open angle glaucoma Immunogenetics and clinical phenotype of sympathetic ophthalmia in British and Irish patients Rhodopsin mutations in Chinese patients with retinitis pigmentosa What is Sorsby's fundus dystrophy? A new pedigree with recessive CHED mapping to the CHED2 locus on 20p13 Genetic testing—swings and roundabouts: a view from the United Kingdom Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreous Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0) Clinical features of a novel TIMP-3 mutation causing Sorsby's fundus dystrophy: implications for disease mechanism The importance of genes and environment for ocular refraction and its determiners: a population based study among 20-45 year old twins Gene therapy for retinopathy of prematurity: the eye is a window to the future X linked dominant congenital isolated bilateral ptosis: the definition and characterisation of a new condition Gene transfer by viral vectors into blood vessels in a rat model of retinopathy of prematurity Factors affecting pupil size after dilatation: the Twin Eye Study

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