Scanga H - Search Results

1

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: scanga h. Eye (Lond). 2023 Nov;37(16):3455-3460. doi: 10.1038/s41433-023-02533-9. Epub 2023 Apr 21. Eye (Lond). 2023. PMID: 37085721

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. 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. Among authors: scanga h. 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. Among authors: scanga h. 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. 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. 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. 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. 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. 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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

33 results

Search Page