Scanga HL - Search Results

1

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

2

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.

3

Improved visual function with dietary intervention in a child with lipemia retinalis.

Fu V, Scanga HL, Medsinge A, Nischal KK. Fu V, et al. Among authors: scanga hl. J AAPOS. 2014 Oct;18(5):488-90. doi: 10.1016/j.jaapos.2014.05.004. Epub 2014 Oct 21. J AAPOS. 2014. PMID: 25439305

4

Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation.

Chauhan BK, Hoover JM, Scanga H, Medsinge A, Arnold GL, Nischal KK. Chauhan BK, et al. Plast Reconstr Surg Glob Open. 2015 Jul 8;3(6):e427. doi: 10.1097/GOX.0000000000000369. eCollection 2015 Jun. Plast Reconstr Surg Glob Open. 2015. PMID: 26180728 Free PMC article.

5

Coenzyme Q10 in the Treatment of Corneal Edema in Kearns-Sayre: Is There an Application in Fuchs Endothelial Corneal Dystrophy?

Kim J, Medsinge A, Chauhan B, Wiest C, Scanga H, Monaghan R, Moore WH, Nischal KK. Kim J, et al. Cornea. 2016 Sep;35(9):1250-4. doi: 10.1097/ICO.0000000000000927. Cornea. 2016. PMID: 27442316 Review.

6

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.

7

Case series: Pyramidal cataracts, intact irides and nystagmus from three novel PAX6 mutations.

Chauhan BK, Medsinge A, Baumgartner MP, Scanga HL, Kamakari S, Gajdosova E, Camacho CJ, Nischal KK. Chauhan BK, et al. Among authors: scanga hl. Am J Ophthalmol Case Rep. 2018 Feb 28;10:172-179. doi: 10.1016/j.ajoc.2018.02.021. eCollection 2018 Jun. Am J Ophthalmol Case Rep. 2018. PMID: 29780932 Free PMC article.

8

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

9

Clinical and imaging characteristics of posterior column ataxia with retinitis pigmentosa with a specific FLVCR1 mutation.

Lee J, Scanga HL, Dansingani KK, Taubenslag KJ, Zlotcavitch L, Chauhan BK, Sylvester CL, Morton DH, Nischal KK. Lee J, et al. Among authors: scanga hl. Ophthalmic Genet. 2018 Dec;39(6):735-740. doi: 10.1080/13816810.2018.1547913. Epub 2018 Nov 16. Ophthalmic Genet. 2018. PMID: 30444160

10

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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