Detalhe da pesquisa
1.
Upregulated Retinal Neurofilament Expression in Experimental Optic Neuritis.
Neuroophthalmology
; 46(4): 215-219, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35859627
2.
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
Am J Hum Genet
; 84(6): 792-800, 2009 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19520207
3.
Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy.
Ophthalmology
; 123(6): 1401-4, 2016 06.
Artigo
Inglês
| MEDLINE | ID: mdl-26854037
4.
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
Arch Ophthalmol
; 128(6): 772-8, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20547956
5.
Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
Ophthalmic Genet
; 30(1): 1-6, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19172503