225 related articles for article (PubMed ID: 35157951)
1. Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Kuht HJ; Maconachie GDE; Han J; Kessel L; van Genderen MM; McLean RJ; Hisaund M; Tu Z; Hertle RW; Gronskov K; Bai D; Wei A; Li W; Jiao Y; Smirnov V; Choi JH; Tobin MD; Sheth V; Purohit R; Dawar B; Girach A; Strul S; May L; Chen FK; Heath Jeffery RC; Aamir A; Sano R; Jin J; Brooks BP; Kohl S; Arveiler B; Montoliu L; Engle EC; Proudlock FA; Nishad G; Pani P; Varma G; Gottlob I; Thomas MG
Ophthalmology; 2022 Jun; 129(6):708-718. PubMed ID: 35157951
[TBL] [Abstract][Full Text] [Related]
2. Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Thomas MG; Kumar A; Mohammad S; Proudlock FA; Engle EC; Andrews C; Chan WM; Thomas S; Gottlob I
Ophthalmology; 2011 Aug; 118(8):1653-60. PubMed ID: 21529956
[TBL] [Abstract][Full Text] [Related]
3. Foveal hypoplasia in parents of patients with albinism.
Lejoyeux R; Alonso AS; Lafolie J; Michaud V; Lasseaux E; Vasseur V; Derrien S; Robert MP; Le Mer Y; Tadayoni R; Arveiler B; Mauget-Faÿsse M
Ophthalmic Genet; 2022 Dec; 43(6):817-823. PubMed ID: 36098180
[TBL] [Abstract][Full Text] [Related]
4. The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences.
Kruijt CC; Gradstein L; Bergen AA; Florijn RJ; Arveiler B; Lasseaux E; Zanlonghi X; Bagdonaite-Bejarano L; Fulton AB; Yahalom C; Blumenfeld A; Perez Y; Birk OS; de Wit GC; Schalij-Delfos NE; van Genderen MM
Invest Ophthalmol Vis Sci; 2022 Jan; 63(1):19. PubMed ID: 35029636
[TBL] [Abstract][Full Text] [Related]
5. Abnormal foveal morphology in ocular albinism imaged with spectral-domain optical coherence tomography.
Chong GT; Farsiu S; Freedman SF; Sarin N; Koreishi AF; Izatt JA; Toth CA
Arch Ophthalmol; 2009 Jan; 127(1):37-44. PubMed ID: 19139336
[TBL] [Abstract][Full Text] [Related]
6. Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism.
Chan HW; Schiff ER; Tailor VK; Malka S; Neveu MM; Theodorou M; Moosajee M
Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33808351
[TBL] [Abstract][Full Text] [Related]
7. Correlation of visual acuity with foveal hypoplasia grading by optical coherence tomography in albinism.
Seo JH; Yu YS; Kim JH; Choung HK; Heo JW; Kim SJ
Ophthalmology; 2007 Aug; 114(8):1547-51. PubMed ID: 17337060
[TBL] [Abstract][Full Text] [Related]
8. Can Structural Grading of Foveal Hypoplasia Predict Future Vision in Infantile Nystagmus?: A Longitudinal Study.
Rufai SR; Thomas MG; Purohit R; Bunce C; Lee H; Proudlock FA; Gottlob I
Ophthalmology; 2020 Apr; 127(4):492-500. PubMed ID: 31937464
[TBL] [Abstract][Full Text] [Related]
9. The Phenotypic Spectrum of Albinism.
Kruijt CC; de Wit GC; Bergen AA; Florijn RJ; Schalij-Delfos NE; van Genderen MM
Ophthalmology; 2018 Dec; 125(12):1953-1960. PubMed ID: 30098354
[TBL] [Abstract][Full Text] [Related]
10. Expanding the Spectrum of Oculocutaneous Albinism: Does Isolated Foveal Hypoplasia Really Exist?
Rocca C; Tiberi L; Bargiacchi S; Palazzo V; Landini S; Marziali E; Caputo R; Tinelli F; Marchi V; Benedetto A; Pagliazzi A; Bacci GM
Int J Mol Sci; 2022 Jul; 23(14):. PubMed ID: 35887175
[TBL] [Abstract][Full Text] [Related]
11. Ocular findings and a comparative study of hair, skin and iris color in Chinese patients with albinism.
Arcot Sadagopan K; Teng CH; Hui G; Lin DL
Ophthalmic Genet; 2023 Feb; 44(1):54-69. PubMed ID: 36316991
[TBL] [Abstract][Full Text] [Related]
12. Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology.
Lee H; Sheth V; Bibi M; Maconachie G; Patel A; McLean RJ; Michaelides M; Thomas MG; Proudlock FA; Gottlob I
Ophthalmology; 2013 Dec; 120(12):2714-2724. PubMed ID: 24161406
[TBL] [Abstract][Full Text] [Related]
13. Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism.
Ehrenberg M; Bagdonite-Bejarano L; Fulton AB; Orenstein N; Yahalom C
Ophthalmic Genet; 2021 Jun; 42(3):243-251. PubMed ID: 33594928
[No Abstract] [Full Text] [Related]
14. Abnormal foveal morphology in carriers of oculocutaneous albinism.
Kuht HJ; Thomas MG; McLean RJ; Sheth V; Proudlock FA; Gottlob I
Br J Ophthalmol; 2023 Aug; 107(8):1202-1208. PubMed ID: 35379600
[TBL] [Abstract][Full Text] [Related]
15. Concentric macular rings sign in patients with foveal hypoplasia.
Cornish KS; Reddy AR; McBain VA
JAMA Ophthalmol; 2014 Sep; 132(9):1084-8. PubMed ID: 24945710
[TBL] [Abstract][Full Text] [Related]
16. Foveal development and nystagmus.
Proudlock F; Gottlob I
Ann N Y Acad Sci; 2011 Sep; 1233():292-7. PubMed ID: 21951007
[TBL] [Abstract][Full Text] [Related]
17. SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization.
Kuht HJ; Han J; Maconachie GDE; Park SE; Lee ST; McLean R; Sheth V; Hisaund M; Dawar B; Sylvius N; Mahmood U; Proudlock FA; Gottlob I; Lim HT; Thomas MG
Hum Mol Genet; 2020 Nov; 29(18):2989-3002. PubMed ID: 32744312
[TBL] [Abstract][Full Text] [Related]
18. Foveal thickness and macular volume in patients with oculocutaneous albinism.
Izquierdo NJ; Emanuelli A; Izquierdo JC; García M; Cadilla C; Berrocal MH
Retina; 2007; 27(9):1227-30. PubMed ID: 18046229
[TBL] [Abstract][Full Text] [Related]
19. Clinical Insights Into Foveal Morphology in Albinism.
McCafferty BK; Wilk MA; McAllister JT; Stepien KE; Dubis AM; Brilliant MH; Anderson JL; Carroll J; Summers CG
J Pediatr Ophthalmol Strabismus; 2015; 52(3):167-72. PubMed ID: 26053207
[TBL] [Abstract][Full Text] [Related]
20. Normal and abnormal foveal development.
Thomas MG; Papageorgiou E; Kuht HJ; Gottlob I
Br J Ophthalmol; 2022 May; 106(5):593-599. PubMed ID: 33148537
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]