199 related articles for article (PubMed ID: 21447990)
21. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
Sustar M; Perovšek D; Cima I; Stirn-Kranjc B; Hawlina M; Brecelj J
Doc Ophthalmol; 2015 Jun; 130(3):165-77. PubMed ID: 25663266
[TBL] [Abstract][Full Text] [Related]
22. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese.
Fuchs S; Nakazawa M; Maw M; Tamai M; Oguchi Y; Gal A
Nat Genet; 1995 Jul; 10(3):360-2. PubMed ID: 7670478
[TBL] [Abstract][Full Text] [Related]
23. Retinal dysfunction in a presymptomatic patient with Huntington's disease.
Knapp J; VanNasdale DA; Ramsey K; Racine J
Doc Ophthalmol; 2018 Jun; 136(3):213-221. PubMed ID: 29691705
[TBL] [Abstract][Full Text] [Related]
24. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
Al Oreany AA; Al Hadlaq A; Schatz P
Graefes Arch Clin Exp Ophthalmol; 2016 Oct; 254(10):1951-1956. PubMed ID: 27084085
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
Hayashi T; Gekka T; Goto-Omoto S; Takeuchi T; Kubo A; Kitahara K
Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923
[TBL] [Abstract][Full Text] [Related]
27. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
Yamamoto S; Sippel KC; Berson EL; Dryja TP
Nat Genet; 1997 Feb; 15(2):175-8. PubMed ID: 9020843
[TBL] [Abstract][Full Text] [Related]
28. Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease.
Oishi A; Akimoto M; Kawagoe N; Mandai M; Takahashi M; Yoshimura N
Am J Ophthalmol; 2007 Sep; 144(3):475-7. PubMed ID: 17765441
[TBL] [Abstract][Full Text] [Related]
29. Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography.
Park SJ; Woo SJ; Park KH; Hwang JM; Chung H
Invest Ophthalmol Vis Sci; 2010 Jul; 51(7):3673-9. PubMed ID: 20164460
[TBL] [Abstract][Full Text] [Related]
30. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
Nakamura M; Ito S; Terasaki H; Miyake Y
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1610-6. PubMed ID: 11381068
[TBL] [Abstract][Full Text] [Related]
31. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
Smirnov VM; Zeitz C; Soumittra N; Audo I; Defoort-Dhellemmes S
Doc Ophthalmol; 2018 Apr; 136(2):135-143. PubMed ID: 29525873
[TBL] [Abstract][Full Text] [Related]
32. Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full-field electroretinography in patients exposed to vigabatrin medication.
Kjellström U; Andréasson S; Ponjavic V
Acta Ophthalmol; 2014 Mar; 92(2):149-57. PubMed ID: 23387307
[TBL] [Abstract][Full Text] [Related]
33. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
[TBL] [Abstract][Full Text] [Related]
34. Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.
Saker S; Morales M; Jhittay H; Wen Y; Amoaku W
Doc Ophthalmol; 2015 Jun; 130(3):231-40. PubMed ID: 25626405
[TBL] [Abstract][Full Text] [Related]
35. Retinal and optic disc atrophy associated with a CACNA1F mutation in a Japanese family.
Nakamura M; Ito S; Piao CH; Terasaki H; Miyake Y
Arch Ophthalmol; 2003 Jul; 121(7):1028-33. PubMed ID: 12860808
[TBL] [Abstract][Full Text] [Related]
36. Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.
Dev Borman A; Ocaka LA; Mackay DS; Ripamonti C; Henderson RH; Moradi P; Hall G; Black GC; Robson AG; Holder GE; Webster AR; Fitzke F; Stockman A; Moore AT
Invest Ophthalmol Vis Sci; 2012 Jun; 53(7):3927-38. PubMed ID: 22570351
[TBL] [Abstract][Full Text] [Related]
37. 1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease.
Yamada T; Matsumoto M; Kadoi C; Nagaki Y; Hayasaka Y; Hayasaka S
Ophthalmic Genet; 1999 Jun; 20(2):117-20. PubMed ID: 10420197
[TBL] [Abstract][Full Text] [Related]
38. Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene.
Fujinami K; Tsunoda K; Nakamura M; Oguchi Y; Miyake Y
Arch Ophthalmol; 2011 Oct; 129(10):1375-6. PubMed ID: 21987685
[No Abstract] [Full Text] [Related]
39. Central retinal findings in Bothnia dystrophy caused by RLBP1 sequence variation.
Burstedt MS; Golovleva I
Arch Ophthalmol; 2010 Aug; 128(8):989-95. PubMed ID: 20696998
[TBL] [Abstract][Full Text] [Related]
40. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
Schatz P; Preising M; Lorenz B; Sander B; Larsen M; Rosenberg T
Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]