132 related articles for article (PubMed ID: 32444022)
1. Signs of Oguchi Disease and Pigmentary Degeneration from Early in Life.
Nishiguchi KM; Kunikata H; Nakazawa T
Ophthalmology; 2020 Jun; 127(6):825. PubMed ID: 32444022
[No Abstract] [Full Text] [Related]
2. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
Nishiguchi KM; Ikeda Y; Fujita K; Kunikata H; Akiho M; Hashimoto K; Hosono K; Kurata K; Koyanagi Y; Akiyama M; Suzuki T; Kawasaki R; Wada Y; Hotta Y; Sonoda KH; Murakami A; Nakazawa M; Nakazawa T; Abe T
Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
[TBL] [Abstract][Full Text] [Related]
3. Progression from Classical Oguchi Disease to Retinitis Pigmentosa after 50 Years.
Nishiguchi KM; Oguchi Y; Nakazawa T
Ophthalmology; 2020 Jan; 127(1):51. PubMed ID: 31864474
[No Abstract] [Full Text] [Related]
4. A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration.
Carrigan M; Duignan E; Humphries P; Palfi A; Kenna PF; Farrar GJ
Br J Ophthalmol; 2016 Apr; 100(4):495-500. PubMed ID: 26472407
[TBL] [Abstract][Full Text] [Related]
5. Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene.
Nakamachi Y; Nakamura M; Fujii S; Yamamoto M; Okubo K
Am J Ophthalmol; 1998 Feb; 125(2):249-51. PubMed ID: 9467455
[TBL] [Abstract][Full Text] [Related]
6. Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.
Liu X; Gao L; Wang G; Long Y; Ren J; Fujinami K; Meng X; Li S
Doc Ophthalmol; 2020 Dec; 141(3):217-226. PubMed ID: 32333190
[TBL] [Abstract][Full Text] [Related]
7. Oguchi disease masked by retinitis pigmentosa.
Sonoyama H; Shinoda K; Ishigami C; Tada Y; Ideta H; Ideta R; Takahashi M; Miyake Y
Doc Ophthalmol; 2011 Oct; 123(2):127-33. PubMed ID: 21922265
[TBL] [Abstract][Full Text] [Related]
8. Hereditary retinitis pigmentosa: recent findings from electroretinography, fundus reflectometry, and psychophysics.
Sandberg MA
Int Ophthalmol Clin; 1980; 20(1):39-52. PubMed ID: 6995379
[No Abstract] [Full Text] [Related]
9. Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.
Tourville A; Michiels C; Condroyer C; Meunier A; Cordonnier M; Sahel JA; Audo I; Abramowicz M; Zeitz C
Ophthalmic Genet; 2019 Apr; 40(2):182-184. PubMed ID: 31063016
[No Abstract] [Full Text] [Related]
10. Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease.
Ballios BG; Weisbrod D; Kohly R; Muni RH; Wright T; Yan P
Doc Ophthalmol; 2020 Oct; 141(2):181-185. PubMed ID: 32146548
[TBL] [Abstract][Full Text] [Related]
11. Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations.
Cassiman C; Spileers W; De Baere E; de Ravel T; Casteels I
Ophthalmic Genet; 2013; 34(1-2):105-8. PubMed ID: 23039133
[TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular characterization of enhanced S-cone syndrome in children.
Hull S; Arno G; Sergouniotis PI; Tiffin P; Borman AD; Chandra A; Robson AG; Holder GE; Webster AR; Moore AT
JAMA Ophthalmol; 2014 Nov; 132(11):1341-9. PubMed ID: 25079116
[TBL] [Abstract][Full Text] [Related]
13. Fundus albipunctatus and other flecked retina syndromes.
Flynn MF; Bohnert D
J Am Optom Assoc; 1999 Sep; 70(9):571-80. PubMed ID: 10547972
[TBL] [Abstract][Full Text] [Related]
14. Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens.
Genead MA; Fishman GA; Lindeman M
Ophthalmic Genet; 2010 Jun; 31(2):66-72. PubMed ID: 20450307
[TBL] [Abstract][Full Text] [Related]
15. Rare case of simultaneous manifestation of pigmented paravenous retinochoroidal atrophy and retinitis pigmentosa in contralateral eye.
Mehrotra N; Khandelwal J; Nagpal M
Indian J Ophthalmol; 2019 Nov; 67(11):1875-1876. PubMed ID: 31638054
[No Abstract] [Full Text] [Related]
16. Mizuo Nakamura Phenomenon.
Kumar V
J Pediatr Ophthalmol Strabismus; 2015; 52(5):320. PubMed ID: 26431559
[No Abstract] [Full Text] [Related]
17. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
Hayashi T; Tsuzuranuki S; Kozaki K; Urashima M; Tsuneoka H
Ophthalmic Res; 2011 Oct; 46(4):175-80. PubMed ID: 21447990
[TBL] [Abstract][Full Text] [Related]
18. Mizuo-Nakamura Phenomenon in a Middle-aged Woman.
Pellerano F; Gonzalez M; Alvarado A
JAMA Ophthalmol; 2018 Sep; 136(9):e182640. PubMed ID: 30242369
[No Abstract] [Full Text] [Related]
19. Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
Zeitz C; Robson AG; Audo I
Prog Retin Eye Res; 2015 Mar; 45():58-110. PubMed ID: 25307992
[TBL] [Abstract][Full Text] [Related]
20. [Diagnostic electroretinography in the young child].
Niemeyer G; Grbovic B; Gloor B
Klin Monbl Augenheilkd; 1993 May; 202(5):417-21. PubMed ID: 8377405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
