178 related articles for article (PubMed ID: 32146548)
1. 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]
2. Two novel compound heterozygous
Pilotto E; Trevisson E; Nacci EB; Longhin E; Guidolin F; Midena E
Eur J Ophthalmol; 2022 Nov; 32(6):NP1-NP5. PubMed ID: 34162253
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Yasmeen A; Rogan PK; Caruso R; Sieving PA; Riazuddin S; Hejtmancik JF
Mol Vis; 2005 Nov; 11():977-85. PubMed ID: 16319817
[TBL] [Abstract][Full Text] [Related]
6. Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease.
Godara P; Cooper RF; Sergouniotis PI; Diederichs MA; Streb MR; Genead MA; McAnany JJ; Webster AR; Moore AT; Dubis AM; Neitz M; Dubra A; Stone EM; Fishman GA; Han DP; Michaelides M; Carroll J
Am J Ophthalmol; 2012 Dec; 154(6):987-1001.e1. PubMed ID: 22959359
[TBL] [Abstract][Full Text] [Related]
7. The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation.
Skorczyk-Werner A; Kocięcki J; Wawrocka A; Wicher K; Krawczyńiski MR
Klin Oczna; 2015; 117(1):27-30. PubMed ID: 26349155
[TBL] [Abstract][Full Text] [Related]
8. A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report.
Deng Z; Fan F; Tang D; Wu Y; Shu Y; Wu K
BMC Ophthalmol; 2022 Mar; 22(1):99. PubMed ID: 35246075
[TBL] [Abstract][Full Text] [Related]
9. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
Hayashi T; Gekka T; Takeuchi T; Goto-Omoto S; Kitahara K
Ophthalmology; 2007 Jan; 114(1):134-41. PubMed ID: 17070587
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Mutation analysis reveals novel and known mutations in SAG gene in first two Egyptian families with Oguchi disease.
Tawfik CA; Elbagoury NM; Khater NI; Essawi ML
BMC Ophthalmol; 2022 May; 22(1):217. PubMed ID: 35549688
[TBL] [Abstract][Full Text] [Related]
12. Genetic analysis and clinical features of three Chinese patients with Oguchi disease.
Wei X; Li H; Wu S; Zhu T; Sui R
Doc Ophthalmol; 2023 Feb; 146(1):17-32. PubMed ID: 36417138
[TBL] [Abstract][Full Text] [Related]
13. Mizuo-Nakamura Phenomena.
Mittal K; Chawla R
Ophthalmic Surg Lasers Imaging Retina; 2016 Nov; 47(11):1068. PubMed ID: 27842204
[TBL] [Abstract][Full Text] [Related]
14. Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease.
Usui T; Ichibe M; Ueki S; Takagi M; Hasegawa S; Abe H; Sekiya K; Nakazawa M
Am J Ophthalmol; 2000 Sep; 130(3):359-61. PubMed ID: 11020420
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
Dryja TP
Am J Ophthalmol; 2000 Nov; 130(5):547-63. PubMed ID: 11078833
[TBL] [Abstract][Full Text] [Related]
16. A 5-year-old Syrian female was born with Oguchi disease: a rare case report.
Habeeb R; Baba M; Bazkke B; Zazo A; Marashi A
Ann Med Surg (Lond); 2023 Apr; 85(4):918-921. PubMed ID: 37113844
[TBL] [Abstract][Full Text] [Related]
17. [Oguchi disease or stationary congenital night blindness: a case report].
Boissonnot M; Robert MF; Gilbert-Dussardier B; Dighiero P
J Fr Ophtalmol; 2007 Jan; 30(1):e2. PubMed ID: 17287664
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.
Waheed NK; Qavi AH; Malik SN; Maria M; Riaz M; Cremers FP; Azam M; Qamar R
Mol Vis; 2012; 18():1253-9. PubMed ID: 22665972
[TBL] [Abstract][Full Text] [Related]
20. Oguchi's disease: two cases and literature review.
Dai Y; Sun T
J Int Med Res; 2021 May; 49(5):3000605211019921. PubMed ID: 34057838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
