advertisement
Tsang SH 65
Showing records 1 to 25 | Display all abstracts from Tsang SH108080 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
108491 Scleral Thickness in Autosomal Dominant Best Vitelliform Macular Dystrophy
Ngo WK
Retinal cases & brief reports 2023; 0:
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
107885 Clinical and Therapeutic Evaluation of the Ten Most Prevalent Mutations
Lopes da Costa B
Biomedicines 2023; 11:
107457 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
107881 TRAP1 Is Expressed in Human Retinal Pigment Epithelial Cells and Is Required to Maintain their Energetic Status
Ramos Rego I
Antioxidants (Basel, Switzerland) 2023; 12:
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Kim AH
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107511 HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
Kong Y
EMBO molecular medicine 2023; 15: e16525
107885 Clinical and Therapeutic Evaluation of the Ten Most Prevalent Mutations
Lopes da Costa B
Biomedicines 2023; 11:
107881 TRAP1 Is Expressed in Human Retinal Pigment Epithelial Cells and Is Required to Maintain their Energetic Status
Silvério D
Antioxidants (Basel, Switzerland) 2023; 12:
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Kolesnikova M
Clinical and Experimental Ophthalmology 2023; 51: 205-216
107511 HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
Liu PK
EMBO molecular medicine 2023; 15: e16525
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
107885 Clinical and Therapeutic Evaluation of the Ten Most Prevalent Mutations
Kolesnikova M
Biomedicines 2023; 11:
108491 Scleral Thickness in Autosomal Dominant Best Vitelliform Macular Dystrophy
Fisher YL
Retinal cases & brief reports 2023; 0:
107885 Clinical and Therapeutic Evaluation of the Ten Most Prevalent Mutations
Kolesnikova M
Biomedicines 2023; 11:
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
107885 Clinical and Therapeutic Evaluation of the Ten Most Prevalent Mutations
Levi SR
Biomedicines 2023; 11:
107881 TRAP1 Is Expressed in Human Retinal Pigment Epithelial Cells and Is Required to Maintain their Energetic Status
Eufrásio MI
Antioxidants (Basel, Switzerland) 2023; 12:
107511 HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
Li Y
EMBO molecular medicine 2023; 15: e16525
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
107437 Effects of medications on hypoxia-inducible factor in the retina: A review
Ngo WK
Clinical and Experimental Ophthalmology 2023; 51: 205-216
