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For: Bhatti TR, Dott M, Yoon PW, Moore CA, Gambrell D, Rasmussen SA. Descriptive epidemiology of infantile cataracts in metropolitan Atlanta, GA, 1968-1998.Arch Pediatr Adolesc Med. 2003;157:341-347. [PMID: 12695229 DOI: 10.1001/archpedi.157.4.341] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
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2 Chen AH, Abu Bakar NF, Arthur P. Comparison of the pediatric vision screening program in 18 countries across five continents.J CurrOphthalmol. 2019;31:357-365. [PMID: 31844783 DOI: 10.1016/j.joco.2019.07.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
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7 Gürsel Özkurt Z, Balsak S, Çamçi MS, Bilgen K, KatranİH, Aslan A, Han ÇÇ.  Approach of Family Physicians to Pediatric Eye Screening in DiyarbakırTurk J Ophthalmol 2019; 49: 25-29. [PMID: 30829022 DOI: 10.4274/tjo.galenos.2018.10829] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
8 Singh VM, Badakere A, Patil-Chhablani P, Kekunnaya R. Profile of congenital cataract in the first year of life from a tertiary care center in South India - A modern series. Indian J Ophthalmol 2021;69:932-6. [PMID: 33727462 DOI: 10.4103/ijo.IJO_1558_20] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Richter L, Flodman P, Barria von-Bischhoffshausen F, Burch D, Brown S, Nguyen L, Turner J, Spence MA, Bateman JB. Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA). Am J Med Genet A 2008;146A:833-42. [PMID: 18302245 DOI: 10.1002/ajmg.a.32236] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 2.5] [Reference Citation Analysis]
10 Wu X, Long E, Lin H, Liu Y. Prevalence and epidemiological characteristics of congenital cataract: a systematic review and meta-analysis. Sci Rep 2016;6:28564. [PMID: 27334676 DOI: 10.1038/srep28564] [Cited by in Crossref: 53] [Cited by in F6Publishing: 44] [Article Influence: 10.6] [Reference Citation Analysis]
11 Haargaard B, Fledelius HC. Down's syndrome and early cataract. Br J Ophthalmol 2006;90:1024-7. [PMID: 16672328 DOI: 10.1136/bjo.2006.090639] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 1.0] [Reference Citation Analysis]
12 Lim Z, Rubab S, Chan YH, Levin AV. Pediatric cataract: the Toronto experience-etiology. Am J Ophthalmol 2010;149:887-92. [PMID: 20430363 DOI: 10.1016/j.ajo.2010.01.012] [Cited by in Crossref: 28] [Cited by in F6Publishing: 18] [Article Influence: 2.5] [Reference Citation Analysis]
13 Lin H, Yang Y, Chen J, Zhong X, Liu Z, Lin Z, Chen W, Luo L, Qu B, Zhang X, Zheng D, Zhan J, Wu H, Wang Z, Geng Y, Xiang W, Chen W, Liu Y; CCPMOH Study Group. Congenital cataract: prevalence and surgery age at Zhongshan Ophthalmic Center (ZOC). PLoS One 2014;9:e101781. [PMID: 24992190 DOI: 10.1371/journal.pone.0101781] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
14 Toli A, Perente A, Labiris G. Evaluation of the red reflex: An overview for the pediatrician. WJM 2021;11:263-77. [DOI: 10.5662/wjm.v11.i5.263] [Reference Citation Analysis]
15 Chen TC, Bhatia LS, Walton DS. Complications of Pediatric Lensectomy in 193 Eyes. Ophthalmic Surg Lasers Imaging Retina 2005;36:6-13. [DOI: 10.3928/15428877-20050101-01] [Cited by in Crossref: 22] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis]
16 Fry M, Wilson GA. Scope for improving congenital cataract blindness prevention by screening of infants (red reflex screening) in a New Zealand setting. J Paediatr Child Health 2005;41:344-6. [PMID: 16014138 DOI: 10.1111/j.1440-1754.2005.00628.x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
17 Choi J, Kim JH, Kim SJ, Yu YS. Clinical characteristics, course, and visual prognosis of partial cataracts that seem to be visually insignificant in children. J AAPOS 2012;16:161-7. [PMID: 22525173 DOI: 10.1016/j.jaapos.2011.10.017] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
18 Cagini C, Tosi G, Stracci F, Rinaldi VE, Verrotti A. Red reflex examination in neonates: evaluation of 3 years of screening.Int Ophthalmol. 2017;37:1199-1204. [PMID: 27822637 DOI: 10.1007/s10792-016-0393-2] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 1.8] [Reference Citation Analysis]
19 Pon JM, Bevin TH, Herbison P, Taylor BJ, Sanderson G. A novel instrument for assessing the retinal red reflex for non‐ophthalmic health professionals. Clinical and Experimental Optometry 2005;88:160-4. [DOI: 10.1111/j.1444-0938.2005.tb06689.x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 Nalbandyan M, Papadopoulos EA, Leckman-Westin E, Browne ML. Nongenetic risk factors for infantile cataracts: Systematic review of observational studies. Birth Defects Res 2021;113:1112-29. [PMID: 33949794 DOI: 10.1002/bdr2.1904] [Reference Citation Analysis]
21 Ibrahim MKM, Wolvaardt JE, Elnimeiri MKM. Risk factors of ocular morbidity among under-five years old children in Khartoum State- Sudan- 2020. Health Sci Rep 2021;4:e279. [PMID: 33977161 DOI: 10.1002/hsr2.279] [Reference Citation Analysis]
22 Prakalapakorn SG, Rasmussen SA, Lambert SR, Honein MA; National Birth Defects Prevention Study. Assessment of risk factors for infantile cataracts using a case-control study: National Birth Defects Prevention Study, 2000-2004. Ophthalmology 2010;117:1500-5. [PMID: 20363508 DOI: 10.1016/j.ophtha.2009.12.026] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
23 Vandenbroucke S, Foets B, Wouters C, Casteels I. Bilateral congenital cataract with suspected lens-induced granulomatous uveitis. J AAPOS 2014;18:492-4. [PMID: 25262559 DOI: 10.1016/j.jaapos.2014.05.010] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
24 Messina-Baas O, Gonzalez-Garay ML, González-Huerta LM, Toral-López J, Cuevas-Covarrubias SA. Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract. Mol Syndromol 2016;7:87-92. [PMID: 27385965 DOI: 10.1159/000445669] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]