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Page 1
IMI-Management and Investigation of High Myopia in Infants and Young Children.
Flitcroft I, Ainsworth J, Chia A, Cotter S, Harb E, Jin ZB, Klaver CCW, Moore AT, Nischal KK, Ohno-Matsui K, Paysse EA, Repka MX, Smirnova IY, Snead M, Verhoeven VJM, Verkicharla PK. Flitcroft I, et al. Among authors: nischal kk. Invest Ophthalmol Vis Sci. 2023 May 1;64(6):3. doi: 10.1167/iovs.64.6.3. Invest Ophthalmol Vis Sci. 2023. PMID: 37126360 Free PMC article.
Thygeson's superficial punctate keratitis in children.
Gagrani M, Conner EA, Scanga H, Hiasat JG, Tripi KS, Pihlblad MS, Jhanji V, Nischal KK. Gagrani M, et al. Among authors: nischal kk. Eye (Lond). 2023 Nov;37(16):3455-3460. doi: 10.1038/s41433-023-02533-9. Epub 2023 Apr 21. Eye (Lond). 2023. PMID: 37085721
Advancing therapies for anterior segment developmental anomalies.
Ramappa M, Nischal KK. Ramappa M, et al. Among authors: nischal kk. Taiwan J Ophthalmol. 2023 Dec 20;13(4):403-404. doi: 10.4103/tjo.TJO-D-23-00167. eCollection 2023 Oct-Dec. Taiwan J Ophthalmol. 2023. PMID: 38249506 Free PMC article. No abstract available.
Congenital corneal staphyloma in 8q21.11 microdeletion syndrome.
Franco E, Scanga HL, Jacob S, Chu CT, Nischal KK. Franco E, et al. Among authors: nischal kk. Ophthalmic Genet. 2023 Apr;44(2):147-151. doi: 10.1080/13816810.2022.2127152. Epub 2022 Nov 7. Ophthalmic Genet. 2023. PMID: 36341706
Optical coherence tomography angiography of choroidal neovascularization in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD).
Wongchaisuwat N, Wang J, Yang P, Everett L, Gregor A, Sahel JA, Nischal KK, Pennesi ME, Gillingham MB, Jia Y. Wongchaisuwat N, et al. Among authors: nischal kk. Am J Ophthalmol Case Rep. 2023 Nov 20;32:101958. doi: 10.1016/j.ajoc.2023.101958. eCollection 2023 Dec. Am J Ophthalmol Case Rep. 2023. PMID: 38161518 Free PMC article.
Congenital Corneal Opacity in 22q11.2 Deletion Syndrome: A Case Series.
Franco E, Iqbal N, Shah PR, Alabek M, Tripi KS, Prescott C, Scanga HL, Chu CT, Nischal KK. Franco E, et al. Among authors: nischal kk. Cornea. 2023 Mar 1;42(3):344-350. doi: 10.1097/ICO.0000000000003155. Epub 2022 Nov 30. Cornea. 2023. PMID: 36455075
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy.
Gillingham MB, Choi D, Gregor A, Wongchaisuwat N, Black D, Scanga HL, Nischal KK, Sahel JA, Arnold G, Vockley J, Harding CO, Pennesi ME. Gillingham MB, et al. Among authors: nischal kk. J Inherit Metab Dis. 2024 Apr 16. doi: 10.1002/jimd.12738. Online ahead of print. J Inherit Metab Dis. 2024. PMID: 38623632
201 results