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Quoted phrase not found in phrase index: "Dominant pericentral pigmentary retinopathy"
Page 1
Pericentral retinal dystrophy.
Grøndahl J. Grøndahl J. Acta Ophthalmol (Copenh). 1987 Jun;65(3):344-51. doi: 10.1111/j.1755-3768.1987.tb08517.x. Acta Ophthalmol (Copenh). 1987. PMID: 3618160
A diagnosis of pericentral retinal dystrophy was made in 28 patients from four families, all living in North Norway. Patients from two and three generations were examined, establishing the relatively benign but progressive course of the disease. The advanced stage o …
A diagnosis of pericentral retinal dystrophy was made in 28 patients from four families, all living in North Norway. Patients from tw …
Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.
Selmer KK, Grøndahl J, Riise R, Brandal K, Braaten O, Bragadottir R, Undlien DE. Selmer KK, et al. Acta Ophthalmol. 2010 May;88(3):323-8. doi: 10.1111/j.1755-3768.2008.01465.x. Epub 2009 Jan 30. Acta Ophthalmol. 2010. PMID: 19183411 Free article.
PURPOSE: This study aimed to identify the genetic cause of autosomal dominant pericentral retinal dystrophy (adPRD) in a large Norwegian family with 35 affected members. ...RESULTS: The ophthalmological examinations revealed an atypical form of retinitis p …
PURPOSE: This study aimed to identify the genetic cause of autosomal dominant pericentral retinal dystrophy (adPRD) in a large …
Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa.
Ballios BG, Place EM, Martinez-Velazquez L, Pierce EA, Comander JI, Huckfeldt RM. Ballios BG, et al. Genes (Basel). 2021 Nov 23;12(12):1853. doi: 10.3390/genes12121853. Genes (Basel). 2021. PMID: 34946802 Free PMC article.
Sector and pericentral are two rare, regional forms of retinitis pigmentosa (RP). ...Finally, we present the longest-reported follow-up for a patient with RHO-associated sector-like RP, showing progression from sectoral to pericentral disease over thre …
Sector and pericentral are two rare, regional forms of retinitis pigmentosa (RP). ...Finally, we present the longest-re …
Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.
Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R. Grøndahl J, et al. Acta Ophthalmol Scand. 2007 May;85(3):287-97. doi: 10.1111/j.1600-0420.2006.00820.x. Acta Ophthalmol Scand. 2007. PMID: 17488458 Free article.
PURPOSE: To examine the clinical picture and molecular genetics of 12 Norwegian families with autosomal dominant retinitis pigmentosa (adRP) in order to achieve a genotype-phenotype correlation. METHODS: In addition to a clinical ophthalmological examination, …
PURPOSE: To examine the clinical picture and molecular genetics of 12 Norwegian families with autosomal dominant retinitis …