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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.
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.
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
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
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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.
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