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Items: 1 to 50 of 263

1.

Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces.

Guimaraes TAC, Capasso JE, Levin AV.

Ophthalmic Genet. 2019 Jun;40(3):213-218. doi: 10.1080/13816810.2019.1622021. Epub 2019 Jul 2.

PMID:
31266384
2.

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, Utz VM, Wang K, Alcorn DM, Brooks BP, Costakos DM, Couser NL, Heon E, Levin AV, Lloyd IC, Morse CL, Schmitt MA, Whitman MC, Traboulsi EI.

J AAPOS. 2019 Jun 21. pii: S1091-8531(19)30129-6. doi: 10.1016/j.jaapos.2019.04.005. [Epub ahead of print]

PMID:
31233830
3.

Central Corneal Thickness in Childhood Cataract.

Thau A, Dawodu O, Mireskandari K, Ali A, Tehrani N, DeBenedictis C, Bhoiwala D, Aultman W, Alnabi WA, Leiby BE, Levin AV.

Cornea. 2019 Aug;38(8):1003-1005. doi: 10.1097/ICO.0000000000001970.

PMID:
31045961
4.

Ocular hypotony: A comprehensive review.

Wang Q, Thau A, Levin AV, Lee D.

Surv Ophthalmol. 2019 Apr 25. pii: S0039-6257(18)30222-4. doi: 10.1016/j.survophthal.2019.04.006. [Epub ahead of print] Review.

PMID:
31029581
5.

An update of ophthalmic management in craniosynostosis.

Ganesh A, Edmond J, Forbes B, Katowitz WR, Nischal KK, Miller M, Levin AV.

J AAPOS. 2019 Apr;23(2):66-76. doi: 10.1016/j.jaapos.2018.10.016. Epub 2019 Mar 27. Review.

PMID:
30928366
6.

Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome.

Day AM, McCulloch CE, Hammill AM, Juhász C, Lo WD, Pinto AL, Miles DK, Fisher BJ, Ball KL, Wilfong AA, Levin AV, Thau AJ, Comi AM; National Institute of Health Sponsor: Rare Disease Clinical Research Consortium (RDCRN) Brain and Vascular Malformation Consortium (BVMC) SWS Investigator Group, Koenig JI, Lawton MT, Marchuk DA, Moses MA, Freedman SF, Pevsner J.

Pediatr Neurol. 2019 Jul;96:30-36. doi: 10.1016/j.pediatrneurol.2018.12.002. Epub 2018 Dec 20.

PMID:
30853154
7.

Ophthalmologic findings in the Cornelia de Lange syndrome.

Shi A, Levin AV.

Ophthalmic Genet. 2019 Feb;40(1):1-6. doi: 10.1080/13816810.2019.1571617. Epub 2019 Feb 15.

PMID:
30767692
8.

Glaucoma and degenerative vitreoretinopathy in a girl with Nicolaides-Baraitser syndrome.

Sethi S, Thau A, Kaplan P, Asher SB, Levin AV.

J AAPOS. 2019 Jan 29. pii: S1091-8531(19)30012-6. doi: 10.1016/j.jaapos.2018.12.002. [Epub ahead of print]

PMID:
30707941
9.

Retinal Findings in Young Children With Increased Intracranial Pressure From Nontraumatic Causes.

Shi A, Kulkarni A, Feldman KW, Weiss A, McCourt EA, Schloff S, Partington M, Forbes B, Geddie BE, Bierbrauer K, Phillips PH, Rogers DL, Abed Alnabi W, Binenbaum G, Levin AV.

Pediatrics. 2019 Feb;143(2). pii: e20181182. doi: 10.1542/peds.2018-1182. Epub 2019 Jan 10.

PMID:
30630868
10.

Traumatic macular retinoschisis in infants and children.

Shouldice M, Al-Khattabi F, Thau A, McIntyre S, Ng WKY, Levin AV.

J AAPOS. 2018 Dec;22(6):433-437.e2. doi: 10.1016/j.jaapos.2018.08.007. Epub 2018 Oct 28.

PMID:
30394342
11.

Ophthalmic manifestations associated with RARB mutations.

Wangtiraumnuay N, Kopinsky S, Iyer P, Capasso J, Whitehead R, Schneider A, Levin AV.

Clin Dysmorphol. 2019 Jan;28(1):46-49. doi: 10.1097/MCD.0000000000000246. No abstract available.

PMID:
30281527
12.

Ocular manifestations of Emanuel syndrome.

Saffren BD, Capasso JE, Zanolli M, Levin AV.

Am J Med Genet A. 2018 Sep;176(9):1964-1967. doi: 10.1002/ajmg.a.40361. Epub 2018 Sep 4.

PMID:
30178914
13.

New classification system for pediatric glaucoma: implications for clinical care and a research registry.

Thau A, Lloyd M, Freedman S, Beck A, Grajewski A, Levin AV.

Curr Opin Ophthalmol. 2018 Sep;29(5):385-394. doi: 10.1097/ICU.0000000000000516. Review.

PMID:
30096087
14.

PATHOLOGY OF PERIMACULAR FOLDS DUE TO VITREORETINAL TRACTION IN ABUSIVE HEAD TRAUMA.

Abed Alnabi W, Tang GJ, Eagle RC Jr, Gulino S, Thau A, Levin AV.

Retina. 2018 Jul 25. doi: 10.1097/IAE.0000000000002273. [Epub ahead of print]

PMID:
30048385
15.

The Eye Examination in the Evaluation of Child Abuse.

Christian CW, Levin AV; COUNCIL ON CHILD ABUSE AND NEGLECT; SECTION ON OPHTHALMOLOGY; AMERICAN ASSOCIATION OF CERTIFIED ORTHOPTISTS; AMERICAN ASSOCIATION FOR PEDIATRIC OPHTHALMOLOGY AND STRABISMUS; AMERICAN ACADEMY OF OPHTHALMOLOGY.

Pediatrics. 2018 Aug;142(2). pii: e20181411. doi: 10.1542/peds.2018-1411. Review.

PMID:
30037976
16.

Efficacy and outcomes of a summer-based pediatric vision screening program.

Hark LA, Shiuey E, Yu M, Tran E, Mayro EL, Zhan T, Pond M, Tran J, Siam L, Levin AV.

J AAPOS. 2018 Aug;22(4):309.e1-309.e7. doi: 10.1016/j.jaapos.2018.04.006. Epub 2018 Aug 8.

PMID:
30012459
17.

Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.

Kline AD, Moss JF, Selicorni A, Bisgaard AM, Deardorff MA, Gillett PM, Ishman SL, Kerr LM, Levin AV, Mulder PA, Ramos FJ, Wierzba J, Ajmone PF, Axtell D, Blagowidow N, Cereda A, Costantino A, Cormier-Daire V, FitzPatrick D, Grados M, Groves L, Guthrie W, Huisman S, Kaiser FJ, Koekkoek G, Levis M, Mariani M, McCleery JP, Menke LA, Metrena A, O'Connor J, Oliver C, Pie J, Piening S, Potter CJ, Quaglio AL, Redeker E, Richman D, Rigamonti C, Shi A, Tümer Z, Van Balkom IDC, Hennekam RC.

Nat Rev Genet. 2018 Oct;19(10):649-666. doi: 10.1038/s41576-018-0031-0. Review.

PMID:
29995837
18.

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Wangtiraumnuay N, Alnabi WA, Tsukikawa M, Thau A, Capasso J, Sharony R, Inglehearn CF, Levin AV.

Ophthalmic Genet. 2018 Jun;39(3):384-390. doi: 10.1080/13816810.2018.1432063. Erratum in: Ophthalmic Genet. 2018 Oct;39(5):669.

PMID:
29676688
19.

Prevalence of uncorrected refractive errors among school-age children in the School District of Philadelphia.

Mayro EL, Hark LA, Shiuey E, Pond M, Siam L, Hill-Bennett T, Tran J, Khanna N, Silverstein M, Donaghy J, Zhan T, Murchison AP, Levin AV.

J AAPOS. 2018 Jun;22(3):214-217.e2. doi: 10.1016/j.jaapos.2018.01.011. Epub 2018 Apr 13.

PMID:
29660392
20.

Ocular manifestations of PACS1 mutation.

Pefkianaki M, Schneider A, Capasso JE, Wasserman BN, Bardakjian T, Levin AV.

J AAPOS. 2018 Aug;22(4):323-325. doi: 10.1016/j.jaapos.2017.12.008. Epub 2018 Mar 14.

PMID:
29550517
21.

Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach.

Petersen-Jones SM, Occelli LM, Winkler PA, Lee W, Sparrow JR, Tsukikawa M, Boye SL, Chiodo V, Capasso JE, Becirovic E, Schön C, Seeliger MW, Levin AV, Michalakis S, Hauswirth WW, Tsang SH.

J Clin Invest. 2018 Jan 2;128(1):190-206. doi: 10.1172/JCI95161. Epub 2017 Nov 20.

22.

Autoimmune retinopathy associated with systemic lupus erythematosus: A diagnostic dilemma.

Wuthisiri W, Lai YH, Capasso J, Blidner M, Salz D, Kruger E, Levin AV.

Taiwan J Ophthalmol. 2017 Jul-Sep;7(3):172-176. doi: 10.4103/tjo.tjo_40_17.

23.

Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma.

Protas ME, Weh E, Footz T, Kasberger J, Baraban SC, Levin AV, Katz LJ, Ritch R, Walter MA, Semina EV, Gould DB.

Hum Mol Genet. 2017 Sep 15;26(18):3630-3638. doi: 10.1093/hmg/ddx251.

24.

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

Dotan G, Karr DJ, Levin AV.

J AAPOS. 2017 Jun;21(3):181.e1-181.e8. doi: 10.1016/j.jaapos.2017.01.004. Epub 2017 May 18.

PMID:
28528992
25.

Effect of anesthesia on intraocular pressure measurement in children.

Mikhail M, Sabri K, Levin AV.

Surv Ophthalmol. 2017 Sep - Oct;62(5):648-658. doi: 10.1016/j.survophthal.2017.04.003. Epub 2017 Apr 22. Review.

PMID:
28438591
26.

Marfan Syndrome: Staging Nonsurgical vs Surgical Treatments in Children With Subluxated Lenses and Refractive Problems.

Paul Chan RV, Khan AO, Levin AV, Paysse EA, DeRespinis PA.

J Pediatr Ophthalmol Strabismus. 2017 Mar 1;54(2):70-73. doi: 10.3928/01913913-20160801-01. No abstract available.

PMID:
28338994
27.

The SBU report: a different view.

Levin AV.

Acta Paediatr. 2017 Jul;106(7):1037-1039. doi: 10.1111/apa.13834. Epub 2017 Apr 19. No abstract available.

PMID:
28301061
28.

Spectral-domain optical coherence tomography findings in Alström syndrome.

Dotan G, Khetan V, Marshall JD, Affel E, Armiger-George D, Naggert JK, Collin GB, Levin AV.

Ophthalmic Genet. 2017 Sep-Oct;38(5):440-445. doi: 10.1080/13816810.2016.1257029. Epub 2017 Jan 23.

29.

Anterior Chamber Pathology in Alagille Syndrome.

Ho DK, Levin AV, Anninger WV, Piccoli DA, Eagle RC Jr.

Ocul Oncol Pathol. 2016 Oct;2(4):270-275. Epub 2016 Jul 2.

30.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, Beyer E, Blumenthal I, Bongers EM, Brilstra EH, Brown CW, Brüggenwirth HT, Callewaert B, Chiang C, Corning K, Cox H, Cuppen E, Currall BB, Cushing T, David D, Deardorff MA, Dheedene A, D'Hooghe M, de Vries BB, Earl DL, Ferguson HL, Fisher H, FitzPatrick DR, Gerrol P, Giachino D, Glessner JT, Gliem T, Grady M, Graham BH, Griffis C, Gripp KW, Gropman AL, Hanson-Kahn A, Harris DJ, Hayden MA, Hill R, Hochstenbach R, Hoffman JD, Hopkin RJ, Hubshman MW, Innes AM, Irons M, Irving M, Jacobsen JC, Janssens S, Jewett T, Johnson JP, Jongmans MC, Kahler SG, Koolen DA, Korzelius J, Kroisel PM, Lacassie Y, Lawless W, Lemyre E, Leppig K, Levin AV, Li H, Li H, Liao EC, Lim C, Lose EJ, Lucente D, Macera MJ, Manavalan P, Mandrile G, Marcelis CL, Margolin L, Mason T, Masser-Frye D, McClellan MW, Mendoza CJ, Menten B, Middelkamp S, Mikami LR, Moe E, Mohammed S, Mononen T, Mortenson ME, Moya G, Nieuwint AW, Ordulu Z, Parkash S, Pauker SP, Pereira S, Perrin D, Phelan K, Aguilar RE, Poddighe PJ, Pregno G, Raskin S, Reis L, Rhead W, Rita D, Renkens I, Roelens F, Ruliera J, Rump P, Schilit SL, Shaheen R, Sparkes R, Spiegel E, Stevens B, Stone MR, Tagoe J, Thakuria JV, van Bon BW, van de Kamp J, van Der Burgt I, van Essen T, van Ravenswaaij-Arts CM, van Roosmalen MJ, Vergult S, Volker-Touw CM, Warburton DP, Waterman MJ, Wiley S, Wilson A, Yerena-de Vega MC, Zori RT, Levy B, Brunner HG, de Leeuw N, Kloosterman WP, Thorland EC, Morton CC, Gusella JF, Talkowski ME.

Nat Genet. 2017 Jan;49(1):36-45. doi: 10.1038/ng.3720. Epub 2016 Nov 14.

31.

Macular cystoid spaces in patients with retinal dystrophy.

Lingao MD, Ganesh A, Karthikeyan AS, Al Zuhaibi S, Al-Hosni A, Al Khayat A, Capasso J, Trumler AA, Stroh E, Al Shekaili H, Cater JR, Levin AV.

Ophthalmic Genet. 2016 Dec;37(4):377-383. Epub 2016 Feb 19.

PMID:
26894784
32.

Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene.

Lai YH, Capasso JE, Kaiser R, Levin AV.

Ophthalmic Genet. 2016 Dec;37(4):424-426. Epub 2016 Feb 19.

PMID:
26894652
33.

Improving access to vision screening in urban Philadelphia elementary schools.

Hark LA, Mayro EL, Tran J, Pond M, Schneider R, Torosian J, Snitzer M, Dabbish N, Levin AV.

J AAPOS. 2016 Oct;20(5):439-443.e1. doi: 10.1016/j.jaapos.2016.07.219. Epub 2016 Sep 16.

PMID:
27647117
34.

The Effectiveness of a Mobile Clinic in Improving Follow-up Eye Care for At-Risk Children.

Diao W, Patel J, Snitzer M, Pond M, Rabinowitz MP, Ceron G, Bagley K, Dennis K, Weiner R, Martinez-Helfman S, Maria KS, Burke B, Aultman WB, Levin AV.

J Pediatr Ophthalmol Strabismus. 2016 Nov 1;53(6):344-348. doi: 10.3928/01913913-20160629-04. Epub 2016 Aug 4.

PMID:
27486729
35.

How genetics works? An illustrative case report.

Khetan V, Zanolli M, Capasso J, Refice NZ, Neeley K, Levin AV.

Indian J Ophthalmol. 2016 May;64(5):399-402. doi: 10.4103/0301-4738.185629. Review.

36.
37.

Teaching ethics to ophthalmology residents: the Halifax Symposium.

Hope WC, LaRoche R, Levin AV.

Can J Ophthalmol. 2016 Jun;51(3):188-9. doi: 10.1016/j.jcjo.2015.10.016. No abstract available.

PMID:
27316266
38.

Spectrum of PEX1 and PEX6 variants in Heimler syndrome.

Smith CE, Poulter JA, Levin AV, Capasso JE, Price S, Ben-Yosef T, Sharony R, Newman WG, Shore RC, Brookes SJ, Mighell AJ, Inglehearn CF.

Eur J Hum Genet. 2016 Nov;24(11):1565-1571. doi: 10.1038/ejhg.2016.62. Epub 2016 Jun 15.

39.

Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research.

Comi AM, Sahin M, Hammill A, Kaplan EH, Juhász C, North P, Ball KL, Levin AV, Cohen B, Morris J, Lo W, Roach ES; 2015 Sturge-Weber Syndrome Research Workshop.

Pediatr Neurol. 2016 May;58:12-24. doi: 10.1016/j.pediatrneurol.2015.11.009. Epub 2016 Mar 16.

40.

Retinal hemorrhage: science versus speculation.

Levin AV.

J AAPOS. 2016 Apr;20(2):93-5. doi: 10.1016/j.jaapos.2016.03.001. No abstract available.

PMID:
27079586
41.

Organophosphate retinopathy.

Pham H, Lingao MD, Ganesh A, Capasso JE, Keep R, Sadagopan KA, Levin AV.

Oman J Ophthalmol. 2016 Jan-Apr;9(1):49-51. doi: 10.4103/0974-620X.176101.

42.

Giant Ocular Horn Occurring in a 10-Year-Old Female.

Armstrong BK, Rabinowitz MP, Levin AV, Eagle RC Jr, Snitzer M, Carrasco J.

Ophthalmic Plast Reconstr Surg. 2017 May/Jun;33(3S Suppl 1):S52-S54. doi: 10.1097/IOP.0000000000000646.

PMID:
26882056
43.

Ethical considerations in gene therapy.

Levin AV.

Ophthalmic Genet. 2016 Sep;37(3):249-51. doi: 10.3109/13816810.2015.1121501. Epub 2016 Feb 8. No abstract available.

PMID:
26854599
44.

Use of the Delphi process in paediatric cataract management.

Serafino M, Trivedi RH, Levin AV, Wilson ME, Nucci P, Lambert SR, Nischal KK, Plager DA, Bremond-Gignac D, Kekunnaya R, Nishina S, Tehrani NN, Ventura MC.

Br J Ophthalmol. 2016 May;100(5):611-5. doi: 10.1136/bjophthalmol-2015-307287. Epub 2015 Sep 29.

PMID:
26420824
45.

Acute Bilateral Leber Hereditary Optic Neuropathy.

Khetan V, Zanolli M, Levin AV.

J Pediatr Ophthalmol Strabismus. 2015 Jul-Aug;52(4):256. doi: 10.3928/01913913-20150709-01. No abstract available.

PMID:
26214724
46.

Peters anomaly in cri-du-chat syndrome.

Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV.

J AAPOS. 2015 Jun;19(3):277-9. doi: 10.1016/j.jaapos.2015.01.018.

PMID:
26059676
47.

Technique for Tube Extender Implantation.

Ho DK, Flannigan KP, Levin AV.

J Glaucoma. 2016 Mar;25(3):e265-7. doi: 10.1097/IJG.0000000000000272.

PMID:
25943733
48.

Early onset ectopia lentis due to a FBN1 mutation with non-penetrance.

Zhang L, Lai YH, Capasso JE, Han S, Levin AV.

Am J Med Genet A. 2015 Jun;167(6):1365-8. doi: 10.1002/ajmg.a.37035. Epub 2015 Apr 21.

PMID:
25900864
49.

The Eagles Eye Mobile: assessing its ability to deliver eye care in a high-risk community.

Alvi RA, Justason L, Liotta C, Martinez-Helfman S, Dennis K, Croker SP, Leiby BE, Levin AV.

J Pediatr Ophthalmol Strabismus. 2015 Mar-Apr;52(2):98-105. doi: 10.3928/01913913-20150216-02.

PMID:
25798708
50.

Sector iris hemangioma in association with diffuse choroidal hemangioma.

Shields CL, Atalay HT, Wuthisiri W, Levin AV, Lally SE, Shields JA.

J AAPOS. 2015 Feb;19(1):83-6. doi: 10.1016/j.jaapos.2014.09.012.

PMID:
25727597

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