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Kim AH 17
Showing records 1 to 17 | Display all abstracts from Kim AH107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Soucy M
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Kolesnikova M
Investigative Ophthalmology and Visual Science 2023; 64: 23
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Kim AH
Clinical and Experimental Ophthalmology 2023; 51: 205-216
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Kolesnikova M
Investigative Ophthalmology and Visual Science 2023; 64: 23
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Kim AH; Kolesnikova M
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kolesnikova M
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Lima de Carvalho JR
Investigative Ophthalmology and Visual Science 2023; 64: 23
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Kolesnikova M
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kolesnikova M
Documenta Ophthalmologica 2023; 146: 267-272
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Ngo WK
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kim AH
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Oh JK
Investigative Ophthalmology and Visual Science 2023; 64: 23
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kim AH
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Soucy M
Investigative Ophthalmology and Visual Science 2023; 64: 23
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Tsang SH
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Tsang SH
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Demirkol A; Kim AH; Kim AH; Tsang SH; Breazzano MP
Investigative Ophthalmology and Visual Science 2023; 64: 23
