708 related articles for article (PubMed ID: 27386845)
41. Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging.
Ritter M; Zotter S; Schmidt WM; Bittner RE; Deak GG; Pircher M; Sacu S; Hitzenberger CK; Schmidt-Erfurth UM;
Invest Ophthalmol Vis Sci; 2013 Sep; 54(9):6416-25. PubMed ID: 23882696
[TBL] [Abstract][Full Text] [Related]
42. Clinical and Genetic Features of Choroideremia in Childhood.
Khan KN; Islam F; Moore AT; Michaelides M
Ophthalmology; 2016 Oct; 123(10):2158-65. PubMed ID: 27506488
[TBL] [Abstract][Full Text] [Related]
43. Retinal Morphology in Sjögren-Larsson Syndrome on OCT: From Metabolic Crystalline Maculopathy to Early-Onset Macular Degeneration.
Staps P; Cruysberg JRM; Roeleveld N; Willemsen MAAP; Theelen T
Ophthalmol Retina; 2019 Jun; 3(6):500-509. PubMed ID: 31174672
[TBL] [Abstract][Full Text] [Related]
44. Sparse scalp hair and vision loss: think hypotrichosis with juvenile macular dystrophy.
Narayan A; Moosajee M
BMJ Case Rep; 2019 Oct; 12(10):. PubMed ID: 31645385
[TBL] [Abstract][Full Text] [Related]
45. Quantitative Fundus Autofluorescence and Optical Coherence Tomography in ABCA4 Carriers.
Duncker T; Stein GE; Lee W; Tsang SH; Zernant J; Bearelly S; Hood DC; Greenstein VC; Delori FC; Allikmets R; Sparrow JR
Invest Ophthalmol Vis Sci; 2015 Nov; 56(12):7274-85. PubMed ID: 26551331
[TBL] [Abstract][Full Text] [Related]
46. Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.
Katagiri S; Hayashi T; Yoshitake K; Akahori M; Ikeo K; Gekka T; Tsuneoka H; Iwata T
Ophthalmic Genet; 2016; 37(1):68-75. PubMed ID: 25113443
[TBL] [Abstract][Full Text] [Related]
47. Atypical retinal pigment epithelial defects with retained photoreceptor layers: a so far disregarded finding in age related macular degeneration.
Giannakaki-Zimmermann H; Querques G; Munch IC; Shroff D; Sarraf D; Chen X; Cunha-Souza E; Mrejen S; Capuano V; Rodrigues MW; Gupta C; Ebneter A; Zinkernagel MS; Munk MR
BMC Ophthalmol; 2017 May; 17(1):67. PubMed ID: 28506260
[TBL] [Abstract][Full Text] [Related]
48. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.
Souied E; Amalric P; Chauvet ML; Chevallier C; Le Hoang P; Munnich A; Kaplan J
Ophthalmic Genet; 1995 Mar; 16(1):11-5. PubMed ID: 7648037
[TBL] [Abstract][Full Text] [Related]
49. Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations.
Wang Y; Sun W; Xiao X; Li S; Jia X; Wang P; Zhang Q
Am J Ophthalmol; 2021 Mar; 223():160-168. PubMed ID: 33342761
[TBL] [Abstract][Full Text] [Related]
50. Long-term follow-up of a patient with JAG1-associated retinopathy.
Cheema MR; Stone LG; Sellar PW; Quinn S; Clark SC; Martin RJ; O'Brien JM; Warriner C; Browning AC
Doc Ophthalmol; 2021 Oct; 143(2):237-247. PubMed ID: 33877487
[TBL] [Abstract][Full Text] [Related]
51. LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13.
Perez-Roustit S; Marquette V; Bocquet B; Kaplan J; Perrault I; Meunier I; Hamel CP
Retin Cases Brief Rep; 2017 Summer; 11(3):221-226. PubMed ID: 27203561
[TBL] [Abstract][Full Text] [Related]
52. Foveal sparing in Stargardt disease.
van Huet RA; Bax NM; Westeneng-Van Haaften SC; Muhamad M; Zonneveld-Vrieling MN; Hoefsloot LH; Cremers FP; Boon CJ; Klevering BJ; Hoyng CB
Invest Ophthalmol Vis Sci; 2014 Oct; 55(11):7467-78. PubMed ID: 25324290
[TBL] [Abstract][Full Text] [Related]
53. Relationship Between Presumptive Inner Nuclear Layer Thickness and Geographic Atrophy Progression in Age-Related Macular Degeneration.
Ebneter A; Jaggi D; Abegg M; Wolf S; Zinkernagel MS
Invest Ophthalmol Vis Sci; 2016 Jul; 57(9):OCT299-306. PubMed ID: 27409486
[TBL] [Abstract][Full Text] [Related]
54. Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.
Chen Y; Ratnam K; Sundquist SM; Lujan B; Ayyagari R; Gudiseva VH; Roorda A; Duncan JL
Invest Ophthalmol Vis Sci; 2011 May; 52(6):3281-92. PubMed ID: 21296825
[TBL] [Abstract][Full Text] [Related]
55. Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy.
Halford S; Holt R; Németh AH; Downes SM
Arch Ophthalmol; 2012 Nov; 130(11):1490-2. PubMed ID: 23143461
[No Abstract] [Full Text] [Related]
56. 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]
57. Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.
Cho SC; Woo SJ; Park KH; Hwang JM
Korean J Ophthalmol; 2013 Feb; 27(1):19-27. PubMed ID: 23372375
[TBL] [Abstract][Full Text] [Related]
58. The absence of fundus abnormalities in Stargardt disease.
Bax NM; Lambertus S; Cremers FPM; Klevering BJ; Hoyng CB
Graefes Arch Clin Exp Ophthalmol; 2019 Jun; 257(6):1147-1157. PubMed ID: 30903310
[TBL] [Abstract][Full Text] [Related]
59. Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Khan KN; Kasilian M; Mahroo OAR; Tanna P; Kalitzeos A; Robson AG; Tsunoda K; Iwata T; Moore AT; Fujinami K; Michaelides M
Ophthalmology; 2018 May; 125(5):735-746. PubMed ID: 29310964
[TBL] [Abstract][Full Text] [Related]
60. Macular dystrophy in Kabuki syndrome due to de novo KMT2D variants: refining the phenotype with multimodal imaging and follow-up over 10 years: insight into pathophysiology.
Vaclavik V; Navarro A; Jacot-Guillarmod A; Bottani A; Sun YJ; Franco JA; Mahajan VB; Smirnov V; Bouvet-Drumare I
Graefes Arch Clin Exp Ophthalmol; 2024 Jun; 262(6):1737-1744. PubMed ID: 38206414
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
