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Year Number of Results
1963 1
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1994 1
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1998 1
1999 3
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2007 3
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Page 1
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 …
Ocular findings in lissencephaly.
Nabi NU, Mezer E, Blaser SI, Levin AA, Buncic JR. Nabi NU, et al. J AAPOS. 2003 Jun;7(3):178-84. doi: 10.1016/s1091-8531(02)42005-8. J AAPOS. 2003. PMID: 12825057
Ocular abnormalities included optic nerve hypoplasia and atrophy, retinal dysplasia, retinal nonattachment, macular hypoplasia, anterior segment malformation, and strabismus. ...
Ocular abnormalities included optic nerve hypoplasia and atrophy, retinal dysplasia, retinal nonattachment, macular hypoplasia …
An attempt to prevent senescence: a mitochondrial approach.
Skulachev VP, Anisimov VN, Antonenko YN, Bakeeva LE, Chernyak BV, Erichev VP, Filenko OF, Kalinina NI, Kapelko VI, Kolosova NG, Kopnin BP, Korshunova GA, Lichinitser MR, Obukhova LA, Pasyukova EG, Pisarenko OI, Roginsky VA, Ruuge EK, Senin II, Severina II, Skulachev MV, Spivak IM, Tashlitsky VN, Tkachuk VA, Vyssokikh MY, Yaguzhinsky LS, Zorov DB. Skulachev VP, et al. Biochim Biophys Acta. 2009 May;1787(5):437-61. doi: 10.1016/j.bbabio.2008.12.008. Epub 2008 Dec 29. Biochim Biophys Acta. 2009. PMID: 19159610 Free article. Review.
SkQ1 manifested a strong therapeutic action on some already pronounced retinopathies, in particular, congenital retinal dysplasia. With drops containing 250 nM SkQ1, vision was restored to 67 of 89 animals (dogs, cats, and horses) that became blind because of a reti …
SkQ1 manifested a strong therapeutic action on some already pronounced retinopathies, in particular, congenital retinal dysplasia
Hereditary renal-retinal dysplasia.
Godel V, Iaina A, Nemet P, Lazar M. Godel V, et al. Doc Ophthalmol. 1980 Oct 15;49(2):347-59. doi: 10.1007/BF01886626. Doc Ophthalmol. 1980. PMID: 7438990
This specific association of the renal and retinal conditions, suggesting a genetic background, is called hereditary renal-retinal dysplasia and is transmitted as an autosomal recessive trait. There are some variations in the type of the retinal degeneration in rena …
This specific association of the renal and retinal conditions, suggesting a genetic background, is called hereditary renal-retinal
Pseudoretinoblastoma: Distribution based on gender, age, and laterality.
Mirzayev I, Gündüz AK, Özalp Ateş FS, Tetik D. Mirzayev I, et al. Eur J Ophthalmol. 2023 Jan;33(1):104-111. doi: 10.1177/11206721221100627. Epub 2022 May 16. Eur J Ophthalmol. 2023. PMID: 35570796
In females, the 3 most common diagnoses included PFV (21.3%), retinal dysplasia, congenital glaucoma, and combined hamartoma (each 6.6%). ...
In females, the 3 most common diagnoses included PFV (21.3%), retinal dysplasia, congenital glaucoma, and combined hamartoma ( …
Light-adapted electroretinograms in optic nerve hypoplasia.
Chaplin C, Borchert MS, Fink C, Garcia-Filion P, McCulloch DL. Chaplin C, et al. Doc Ophthalmol. 2009 Oct;119(2):123-32. doi: 10.1007/s10633-009-9188-3. Epub 2009 Aug 11. Doc Ophthalmol. 2009. PMID: 19669817
Genetic factors in lissencephaly syndromes: a review.
Miny P, Holzgreve W, Horst J. Miny P, et al. Childs Nerv Syst. 1993 Nov;9(7):413-7. doi: 10.1007/BF00306195. Childs Nerv Syst. 1993. PMID: 8306358 Review.
Type I lissencephaly in the Miller-Dieker syndrome (MDS) and the isolated lissencephaly sequence (ILS) is differentiated from type II lissencephaly in the Walker-Warburg (hydrocephalus, agyria, retinal dysplasia with or without encephalocele, HARD +/- E) syndrome an …
Type I lissencephaly in the Miller-Dieker syndrome (MDS) and the isolated lissencephaly sequence (ILS) is differentiated from type II lissen …
A biochemical approach to the problem of aging: "megaproject" on membrane-penetrating ions. The first results and prospects.
Skulachev VP. Skulachev VP. Biochemistry (Mosc). 2007 Dec;72(12):1385-96. doi: 10.1134/s0006297907120139. Biochemistry (Mosc). 2007. PMID: 18205623 Free article. Review.
SkQ1 manifests a strong therapeutic action on some already developed retinopathies, in particular, congenital retinal dysplasia. With drops containing 250 nM SkQ1, vision is recovered in 50 of 66 animals who became blind because of retinopathy. ...
SkQ1 manifests a strong therapeutic action on some already developed retinopathies, in particular, congenital retinal dysplasia
Congenital muscular dystrophy-dystroglycanopathy, type A, featuring bilateral retinal dysplasia and vertical angle kappa.
Peiris TJ, Indaram M, Koo E, Soul JS, Hunter DG. Peiris TJ, et al. J AAPOS. 2018 Jun;22(3):242-244.e1. doi: 10.1016/j.jaapos.2017.12.011. Epub 2018 Mar 16. J AAPOS. 2018. PMID: 29555514
In addition, the patient had poor visual acuity, nystagmus, optic nerve hypoplasia, bilateral retinal dysplasia and retinal dragging with a large vertical angle kappa, and an avascular peripheral retina. ...
In addition, the patient had poor visual acuity, nystagmus, optic nerve hypoplasia, bilateral retinal dysplasia and retinal dr …
35 results