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Developing a pediatric ophthalmology telemedicine program in the COVID-19 crisis.
Kapoor S, Eldib A, Hiasat J, Scanga H, Tomasello J, Alabek M, Ament K, Arner D, Benson A, Berret K, Blaha B, Brinza M, Caterino R, Chauhan B, Churchfield W, Fulwylie C, Gruszewski J, Hrinak D, Johnston L, Meyer C, Nanda K, Newton T, Pomycala B, Runkel L, Sanchez K, Skellett S, Steigerwald J, Mitchell E, Pihlblad M, Luchansky C, Keim E, Yu J, Quinn P, Mittal A, Pitetti R, Patil-Chhablani P, Liasis A, Nischal KK. Kapoor S, et al. Among authors: scanga h. J AAPOS. 2020 Aug;24(4):204-208.e2. doi: 10.1016/j.jaapos.2020.05.008. Epub 2020 Sep 2. J AAPOS. 2020. PMID: 32890736 Free PMC article.
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.
Reply.
Nischal KK, Scanga HL, Kim J. Nischal KK, et al. Cornea. 2016 Dec;35(12):e40-e41. doi: 10.1097/ICO.0000000000001041. Cornea. 2016. PMID: 28398931 No abstract available.
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. 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
34 results