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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1964 1
1965 1
1966 1
1969 1
1971 1
1975 1
1976 2
1977 1
1978 1
1980 2
1981 1
1985 3
1986 2
1987 1
1988 2
1989 3
1990 1
1992 1
1993 3
1994 1
1995 1
1996 6
1997 1
1998 3
1999 4
2000 1
2001 4
2004 4
2005 1
2006 1
2007 5
2008 1
2009 1
2010 4
2011 5
2012 4
2014 3
2015 5
2016 3
2017 2
2018 2
2019 1
2020 4
2021 3
2022 3
2023 3
2024 0

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98 results

Results by year

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Page 1
Fundus hemorrhages in infancy.
Kaur B, Taylor D. Kaur B, et al. Surv Ophthalmol. 1992 Jul-Aug;37(1):1-17. doi: 10.1016/0039-6257(92)90002-b. Surv Ophthalmol. 1992. PMID: 1509354 Review.
While neonatal retinal hemorrhages related to birth trauma are common, benign, and self-limited, other retinal hemorrhages in infancy may signify intracranial aneurysms, accidental or non-accidental injury, and a variety of ocular (e.g., Coats' disease, PHPV, ROP, retinal …
While neonatal retinal hemorrhages related to birth trauma are common, benign, and self-limited, other retinal hemorrhages in infancy may si …
Retinal dysplasia.
Snell AC. Snell AC. Am J Ophthalmol. 1965 Oct;60(4):621-7. doi: 10.1016/0002-9394(65)92250-6. Am J Ophthalmol. 1965. PMID: 5897719 No abstract available.
RETINAL DYSPLASIA.
RICKS RM, RIFFENBURGH RS. RICKS RM, et al. Arch Ophthalmol. 1964 Nov;72:637-41. doi: 10.1001/archopht.1964.00970020637010. Arch Ophthalmol. 1964. PMID: 14196747 No abstract available.
Complex microphthalmos.
Weiss AH, Kousseff BG, Ross EA, Longbottom J. Weiss AH, et al. Arch Ophthalmol. 1989 Nov;107(11):1619-24. doi: 10.1001/archopht.1989.01070020697031. Arch Ophthalmol. 1989. PMID: 2818283
Three had anterior segment dysgenesis; 4, congenital lens abnormalities; 14, chorioretinal colobomas; 12, persistent hyperplastic primary vitreous; 4, retinal dysplasia; and 3, complex malformations due to ipsilateral facial malformations. ...
Three had anterior segment dysgenesis; 4, congenital lens abnormalities; 14, chorioretinal colobomas; 12, persistent hyperplastic primary vi …
The Final Diagnosis: Retinoblastoma or Pseudoretinoblastoma.
Mirzayev I, Gündüz AK, Biçer Ö, Tarlan B. Mirzayev I, et al. J Pediatr Ophthalmol Strabismus. 2021 May-Jun;58(3):161-167. doi: 10.3928/01913913-20210108-01. Epub 2021 May 1. J Pediatr Ophthalmol Strabismus. 2021. PMID: 34039153
The most common diagnoses among patients with pseudoretinoblastoma younger than 1 year were persistent fetal vasculature (PFV) (n = 19; 28.8%), Coats disease (n = 7; 10.6%), chorioretinal coloboma (n = 4; 6.1%), retinal dysplasia (n = 4; 6.1%), and retinal detachmen …
The most common diagnoses among patients with pseudoretinoblastoma younger than 1 year were persistent fetal vasculature (PFV) (n = 19; 28.8 …
Atelencephalic aprosencephaly.
Harris CP, Townsend JJ, Norman MG, White VA, Viskochil DH, Pysher TJ, Klatt EC. Harris CP, et al. J Child Neurol. 1994 Oct;9(4):412-6. doi: 10.1177/088307389400900416. J Child Neurol. 1994. PMID: 7822735
The optic globes were completely formed and attached to hypoplastic optic nerves, but retinal dysplasia was apparent histologically in both cases, and bilateral colobomata were present in one case. ...
The optic globes were completely formed and attached to hypoplastic optic nerves, but retinal dysplasia was apparent histologi …
US and MRI of pediatric ocular masses with histopathological correlation.
Brennan RC, Wilson MW, Kaste S, Helton KJ, McCarville MB. Brennan RC, et al. Pediatr Radiol. 2012 Jun;42(6):738-49. doi: 10.1007/s00247-012-2374-6. Epub 2012 Mar 31. Pediatr Radiol. 2012. PMID: 22466750 Free PMC article. Review.
After presenting the imaging anatomy of the normal eye, we discuss pertinent clinical and pathological features, and illustrate the US and MRI appearance of retinoblastoma, medulloepithelioma, uveal melanoma, persistent fetal vasculature, Coats disease, corneal dermoid, retina …
After presenting the imaging anatomy of the normal eye, we discuss pertinent clinical and pathological features, and illustrate the US and M …
Retinal dysplasia of holoprosencephaly.
Gorovoy IR, Layer N, de Alba Campomanes AG. Gorovoy IR, et al. J Pediatr Ophthalmol Strabismus. 2014 Mar 4;51 Online:e16-8. doi: 10.3928/01913913-20140225-03. J Pediatr Ophthalmol Strabismus. 2014. PMID: 25314309
Retinal dysplasia occurs in the setting of sporadic and syndromic holoprosencephaly, which often has associated ocular malformations. ...The authors present the fundus images of a patient with severe holoprosencephaly with retinal dysplasia and bilater …
Retinal dysplasia occurs in the setting of sporadic and syndromic holoprosencephaly, which often has associated ocular malform …
Unilateral retinal dysplasia simulating retinoblastoma.
Saluja G, Lomi N, Kashyap S. Saluja G, et al. BMJ Case Rep. 2020 Sep 16;13(9):e238463. doi: 10.1136/bcr-2020-238463. BMJ Case Rep. 2020. PMID: 32938657 Free PMC article. No abstract available.
98 results