Drack AV - Search Results

1

Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task Force.

Drack AV, Miraldi Utz V, Wang K, Alcorn DM, Brooks BP, Costakos DM, Couser NL, Heon E, Levin AV, Lloyd IC, Morse CL, Schmitt MA, Whitman MC, Traboulsi EI. Drack AV, et al. J AAPOS. 2019 Aug;23(4):226-228.e1. doi: 10.1016/j.jaapos.2019.04.005. Epub 2019 Jun 21. J AAPOS. 2019. PMID: 31233830

2

Progression of retinopathy in olivopontocerebellar atrophy with retinal degeneration.

Drack AV, Traboulsi EI, Maumenee IH. Drack AV, et al. Arch Ophthalmol. 1992 May;110(5):712-3. doi: 10.1001/archopht.1992.01080170134041. Arch Ophthalmol. 1992. PMID: 1580852 No abstract available.

3

Systemic associations of pigmentary retinopathy.

Drack AV, Traboulsi EI. Drack AV, et al. Int Ophthalmol Clin. 1991 Summer;31(3):35-59. doi: 10.1097/00004397-199103130-00006. Int Ophthalmol Clin. 1991. PMID: 1880001 Review. No abstract available.

4

Potential use of LASIK in children.

Drack A, Alcorn D, Lingua R. Drack A, et al. J Pediatr Ophthalmol Strabismus. 2000 Nov-Dec;37(6):354-60. J Pediatr Ophthalmol Strabismus. 2000. PMID: 11392410 No abstract available.

5

Which Leber congenital amaurosis patients are eligible for gene therapy trials?

Drack AV, Johnston R, Stone EM. Drack AV, et al. J AAPOS. 2009 Oct;13(5):463-5. doi: 10.1016/j.jaapos.2009.08.006. J AAPOS. 2009. PMID: 19840725 Free PMC article.

6

Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.

Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, Traboulsi EI, Weleber RG, Pennesi ME, Heon E, Drack A, Lam BL, Allikmets R, Stone EM. Walia S, et al. Ophthalmology. 2010 Jun;117(6):1190-8. doi: 10.1016/j.ophtha.2009.09.056. Epub 2010 Jan 15. Ophthalmology. 2010. PMID: 20079931

7

From the laboratory to the clinic: molecular genetic testing in pediatric ophthalmology.

Drack AV, Lambert SR, Stone EM. Drack AV, et al. Am J Ophthalmol. 2010 Jan;149(1):10-17. doi: 10.1016/j.ajo.2009.08.038. Am J Ophthalmol. 2010. PMID: 20103038 Free PMC article.

8

Recommendations for genetic testing of inherited eye diseases: report of the American Academy of Ophthalmology task force on genetic testing.

Stone EM, Aldave AJ, Drack AV, Maccumber MW, Sheffield VC, Traboulsi E, Weleber RG. Stone EM, et al. Among authors: drack av. Ophthalmology. 2012 Nov;119(11):2408-10. doi: 10.1016/j.ophtha.2012.05.047. Epub 2012 Sep 1. Ophthalmology. 2012. PMID: 22944025

9

Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290.

McAnany JJ, Genead MA, Walia S, Drack AV, Stone EM, Koenekoop RK, Traboulsi EI, Smith A, Weleber RG, Jacobson SG, Fishman GA. McAnany JJ, et al. Among authors: drack av. JAMA Ophthalmol. 2013 Feb;131(2):178-82. doi: 10.1001/2013.jamaophthalmol.354. JAMA Ophthalmol. 2013. PMID: 23411883 Free PMC article.

10

Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.

Seo S, Mullins RF, Dumitrescu AV, Bhattarai S, Gratie D, Wang K, Stone EM, Sheffield V, Drack AV. Seo S, et al. Among authors: drack av. Invest Ophthalmol Vis Sci. 2013 Sep 11;54(9):6118-32. doi: 10.1167/iovs.13-11673. Invest Ophthalmol Vis Sci. 2013. PMID: 23900607 Free PMC article.

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