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Year Number of Results
2014 2
2016 1
2018 3
2019 2
2020 1
2021 6
2022 7
2023 6
2024 4

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Scanga HL, Nischal KK. Scanga HL, et al. J AAPOS. 2020 Feb;24(1):60-61. doi: 10.1016/j.jaapos.2020.01.001. Epub 2020 Jan 27. J AAPOS. 2020. PMID: 32001368 No abstract available.
Reply.
Nischal KK, Scanga HL, Kim J. Nischal KK, et al. Among authors: scanga hl. Cornea. 2016 Dec;35(12):e40-e41. doi: 10.1097/ICO.0000000000001041. Cornea. 2016. PMID: 28398931 No abstract available.
Congenital primary aphakia.
Ernst J, Medsinge A, Scanga HL, Hiasat J, Moore W, Ali A, Levin AV, Stahl ED, Nischal KK. Ernst J, et al. Among authors: scanga hl. J AAPOS. 2022 Feb;26(1):4.e1-4.e5. doi: 10.1016/j.jaapos.2021.09.008. Epub 2022 Jan 17. J AAPOS. 2022. PMID: 35051625
Genetics and ocular disorders: a focused review.
Scanga HL, Nischal KK. Scanga HL, et al. Pediatr Clin North Am. 2014 Jun;61(3):555-65. doi: 10.1016/j.pcl.2014.03.005. Epub 2014 Apr 13. Pediatr Clin North Am. 2014. PMID: 24852152 Review.
Congenital corneal staphyloma in 8q21.11 microdeletion syndrome.
Franco E, Scanga HL, Jacob S, Chu CT, Nischal KK. Franco E, et al. Among authors: scanga hl. Ophthalmic Genet. 2023 Apr;44(2):147-151. doi: 10.1080/13816810.2022.2127152. Epub 2022 Nov 7. Ophthalmic Genet. 2023. PMID: 36341706
Personalized pediatric ophthalmology: a case report.
To LK, Shah PR, Scanga HL, Franks AL, Cladis FP, Nischal KK. To LK, et al. Among authors: scanga hl. J AAPOS. 2019 Aug;23(4):234-236. doi: 10.1016/j.jaapos.2019.03.003. Epub 2019 May 23. J AAPOS. 2019. PMID: 31129100
Macular atrophy in JAG1-related Alagille syndrome: a case series.
Paez-Escamilla M, Scanga HL, Liasis A, Nischal KK. Paez-Escamilla M, et al. Among authors: scanga hl. Ophthalmic Genet. 2022 Apr;43(2):230-234. doi: 10.1080/13816810.2021.2004432. Epub 2021 Dec 10. Ophthalmic Genet. 2022. PMID: 34886763
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: scanga hl. Cornea. 2023 Mar 1;42(3):344-350. doi: 10.1097/ICO.0000000000003155. Epub 2022 Nov 30. Cornea. 2023. PMID: 36455075
Keratoconus in a child with partial trisomy 13.
Ernst J, Eldib A, Scanga HL, Nischal KK. Ernst J, et al. Among authors: scanga hl. Ophthalmic Genet. 2021 Jun;42(3):360-363. doi: 10.1080/13816810.2021.1897849. Epub 2021 Apr 16. Ophthalmic Genet. 2021. PMID: 33858272
Iris anomalies and the incidence of ACTA2 mutation.
Taubenslag KJ, Scanga HL, Huey J, Lee J, Medsinge A, Sylvester CL, Cheng KP, Nischal KK. Taubenslag KJ, et al. Among authors: scanga hl. Br J Ophthalmol. 2019 Apr;103(4):499-503. doi: 10.1136/bjophthalmol-2018-312306. Epub 2018 Jun 6. Br J Ophthalmol. 2019. PMID: 29875232
25 results