Levin 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. Among authors: levin av. 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

In memoriam Maria Musarella.

Héon E, Levin A, MacDonald IM. Héon E, et al. Ophthalmic Genet. 2014 Sep;35(3):129. doi: 10.3109/13816810.2014.907922. Epub 2014 Apr 21. Ophthalmic Genet. 2014. PMID: 24749744 No abstract available.

3

Ocular Genetics Program: multidisciplinary care of patients with ocular genetic eye disease.

Morad Y, Sutherland J, DaSilva L, Ulster A, Shik J, Gallie B, Héon E, Levin AV. Morad Y, et al. Among authors: levin av. Can J Ophthalmol. 2007 Oct;42(5):734-8. doi: 10.3129/i07-144. Can J Ophthalmol. 2007. PMID: 17891201

4

Ocular manifestations of the Johanson-Blizzard syndrome.

Cheung JC, Thomson H, Buncic JR, Héon E, Levin AV. Cheung JC, et al. Among authors: levin av. J AAPOS. 2009 Oct;13(5):512-4. doi: 10.1016/j.jaapos.2009.05.005. Epub 2009 Aug 29. J AAPOS. 2009. PMID: 19717322 Review.

5

Utility of molecular testing for related retinal dystrophies.

Mezer E, Sutherland J, Goei SL, Héon E, Levin AV. Mezer E, et al. Among authors: levin av. Can J Ophthalmol. 2006 Apr;41(2):190-6. doi: 10.1139/I06-007. Can J Ophthalmol. 2006. PMID: 16767206

6

Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene.

Cordovez JA, Traboulsi EI, Capasso JE, Sadagopan KA, Ganesh A, Rychwalski PJ, Neely KA, Brodie SE, Levin AV. Cordovez JA, et al. Among authors: levin av. Ophthalmic Genet. 2015;36(3):257-64. doi: 10.3109/13816810.2014.881505. Ophthalmic Genet. 2015. PMID: 24512366

7

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Vincent AL, et al. Among authors: levin av. Am J Hum Genet. 2002 Feb;70(2):448-60. doi: 10.1086/338709. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774072 Free PMC article.

8

Pediatric ophthalmology and strabismus fellowship Match outcomes, 2000-2015.

Dotan G, Karr DJ, Levin AV. Dotan G, et al. Among authors: levin av. J AAPOS. 2017 Jun;21(3):181.e1-181.e8. doi: 10.1016/j.jaapos.2017.01.004. Epub 2017 May 18. J AAPOS. 2017. PMID: 28528992

9

Further support of the role of CYP1B1 in patients with Peters anomaly.

Vincent A, Billingsley G, Priston M, Glaser T, Oliver E, Walter M, Ritch R, Levin A, Heon E. Vincent A, et al. Mol Vis. 2006 May 16;12:506-10. Mol Vis. 2006. PMID: 16735991 Free article.

10

An update of ophthalmic management in craniosynostosis.

Ganesh A, Edmond J, Forbes B, Katowitz WR, Nischal KK, Miller M, Levin AV. Ganesh A, et al. Among authors: levin av. J AAPOS. 2019 Apr;23(2):66-76. doi: 10.1016/j.jaapos.2018.10.016. Epub 2019 Mar 27. J AAPOS. 2019. PMID: 30928366 Review.

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