 | Articles: Basic Science/Genetics |
Identification of Mutations in the SLC4A11 Gene in Patients With Recessive Congenital Hereditary Endothelial Dystrophy
Archives of Ophthalmology, 05/16/08
Novel SOX2 Mutation Associated With Ocular Coloboma in a Chinese Family
Archives of Ophthalmology, 05/16/08
Relationship between Diabetic Macular Edema and Peripheral Th1/Th2 Balance
Ophthalmologica, 05/16/08
Hyalocyte proliferation and ECM accumulation modulated by bFGF and TGF-(beta)-1
Graefe's Archive for Clinical and Experimental Ophthalmology, 05/15/08
Phenotypic non-penetrance in granular corneal dystrophy type II
Graefe's Archive for Clinical and Experimental Ophthalmology, 05/15/08
Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients
Eye, 05/14/08
Brain barrier dysfunction in Cuban Epidemic Optic Neuropathy
European Journal of Neurology, 05/14/08
Estrogen Receptor Alpha and Matrix Metalloproteinase 2 Polymorphisms and Age-related Maculopathy in Older Women
American Journal of Epidemiology, 05/13/08
Vision Assessment of Nonverbal Patients
American Orthoptic Journal, 05/12/08
Role of BIGH3 R124H mutation in the diagnosis of Avellino corneal dystrophy
European Journal of Ophthalmology, 05/12/08
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Indexed Journals: American Journal of Ophthalmology, Retina, Eye, Cornea
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