Similar articles for PMID: 26731204

Year	Number of Results
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1

Retinopathy of Prematurity Versus Familial Exudative Vitreoretinopathy: Report on Clinical and Angiographic Findings.

John VJ, McClintic JI, Hess DJ, Berrocal AM. John VJ, et al. Ophthalmic Surg Lasers Imaging Retina. 2016 Jan;47(1):14-9. doi: 10.3928/23258160-20151214-02. Ophthalmic Surg Lasers Imaging Retina. 2016. PMID: 26731204

2

Unrecognized ROPER in a child with a novel pathogenic variant in ZNF408 gene.

Tanenbaum R, Acon D, El Hamichi S, Negron C, Berrocal AM. Tanenbaum R, et al. Ophthalmic Genet. 2023 Apr;44(2):171-174. doi: 10.1080/13816810.2020.1778735. Epub 2020 Jun 12. Ophthalmic Genet. 2023. PMID: 32530348

3

Macular Retinal Pigment Epithelial Clumping Leading to a Diagnosis of FEVR.

Tanenbaum R, Acon D, Rodriguez A, Negron C, Berrocal A. Tanenbaum R, et al. Ophthalmic Surg Lasers Imaging Retina. 2021 Sep;52(9):505-508. doi: 10.3928/23258160-20210819-01. Epub 2021 Sep 1. Ophthalmic Surg Lasers Imaging Retina. 2021. PMID: 34505810

4

High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.

Kashani AH, Learned D, Nudleman E, Drenser KA, Capone A, Trese MT. Kashani AH, et al. Ophthalmology. 2014 Jan;121(1):262-268. doi: 10.1016/j.ophtha.2013.08.010. Epub 2013 Sep 29. Ophthalmology. 2014. PMID: 24084499

5

Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).

López-Cañizares A, Lazzarini TA, Mendoza C, Berrocal AM. López-Cañizares A, et al. Ophthalmic Genet. 2023 Jun;44(3):313-317. doi: 10.1080/13816810.2022.2116648. Epub 2022 Nov 29. Ophthalmic Genet. 2023. PMID: 36444989

6

Familial exudative vitreoretinopathy in a premature child.

Gologorsky D, Chang JS, Hess DJ, Berrocal AM. Gologorsky D, et al. Ophthalmic Surg Lasers Imaging Retina. 2013 Nov 1;44(6):603-5. doi: 10.3928/23258160-20131015-04. Epub 2013 Oct 24. Ophthalmic Surg Lasers Imaging Retina. 2013. PMID: 24144178

7

Diversity of retinal vascular anomalies in patients with familial exudative vitreoretinopathy.

Kashani AH, Brown KT, Chang E, Drenser KA, Capone A, Trese MT. Kashani AH, et al. Ophthalmology. 2014 Nov;121(11):2220-7. doi: 10.1016/j.ophtha.2014.05.029. Epub 2014 Jul 5. Ophthalmology. 2014. PMID: 25005911

8

Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome.

Hoyek S, Wang M, Berrocal AM, Wong A, Place EM, Mason-Suares H, Lin AE, Mukai S, Patel NA. Hoyek S, et al. Ophthalmic Genet. 2023 Apr;44(2):198-203. doi: 10.1080/13816810.2022.2098987. Epub 2022 Jul 14. Ophthalmic Genet. 2023. PMID: 35834361

9

Foveal hypoplasia and characteristics of optical components in patients with familial exudative vitreoretinopathy and retinopathy of prematurity.

Chen PY, Kang EY, Chen KJ, Ling XC, Chang YH, Wang NK, Liu L, Chen YP, Hwang YS, Lai CC, Wu WC. Chen PY, et al. Sci Rep. 2022 May 11;12(1):7694. doi: 10.1038/s41598-022-11455-7. Sci Rep. 2022. PMID: 35546162 Free PMC article.

10

Management of avascular peripheral retina in older prematurely born infants.

Ho LY, Ho V, Aggarwal H, Ranchod TM, Capone A Jr, Trese MT, Drenser KA. Ho LY, et al. Retina. 2011 Jul-Aug;31(7):1248-54. doi: 10.1097/IAE.0b013e31820d3f70. Retina. 2011. PMID: 21358456

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