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Year Number of Results
1963 2
1967 1
1968 4
1969 8
1970 3
1971 9
1972 7
1973 7
1974 8
1975 6
1976 9
1977 5
1978 3
1979 5
1980 3
1981 7
1982 6
1983 7
1984 9
1985 12
1986 9
1987 14
1988 36
1989 49
1990 40
1991 40
1992 61
1993 52
1994 46
1995 67
1996 46
1997 52
1998 53
1999 60
2000 62
2001 59
2002 52
2003 55
2004 43
2005 66
2006 52
2007 87
2008 76
2009 67
2010 67
2011 75
2012 75
2013 82
2014 92
2015 75
2016 105
2017 103
2018 117
2019 85
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2022 126
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2024 3

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2,498 results

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The following terms were not found in PubMed: pigmentosa-intellectual, disability-deafness-hypogenitalism
Page 1
Non-syndromic retinitis pigmentosa.
Verbakel SK, van Huet RAC, Boon CJF, den Hollander AI, Collin RWJ, Klaver CCW, Hoyng CB, Roepman R, Klevering BJ. Verbakel SK, et al. Prog Retin Eye Res. 2018 Sep;66:157-186. doi: 10.1016/j.preteyeres.2018.03.005. Epub 2018 Mar 27. Prog Retin Eye Res. 2018. PMID: 29597005 Free article. Review.
Retinitis pigmentosa (RP) encompasses a group of inherited retinal dystrophies characterized by the primary degeneration of rod and cone photoreceptors. ...In addition, we discuss the genes involved in the pathogenesis of RP, as well as the retinal processes …
Retinitis pigmentosa (RP) encompasses a group of inherited retinal dystrophies characterized by the primary degeneration of ro …
Retinitis Pigmentosa (Non-syndromic).
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:125-130. doi: 10.1007/978-3-319-95046-4_25. Adv Exp Med Biol. 2018. PMID: 30578498 Review.
Most of the genes causing autosomal recessive retinitis pigmentosa (AR-RP) are rare and cause 1% of all cases. Some of the genes, like PDE6 (PDE6A, PDE6B, PDE6G), RP25, and RPE65, have higher prevalence, about 2-5% of all cases. ...The ring is suggestive of increased metab …
Most of the genes causing autosomal recessive retinitis pigmentosa (AR-RP) are rare and cause 1% of all cases. Some of the genes, lik …
Cytomegalovirus Retinitis: A Review.
Port AD, Orlin A, Kiss S, Patel S, D'Amico DJ, Gupta MP. Port AD, et al. J Ocul Pharmacol Ther. 2017 May;33(4):224-234. doi: 10.1089/jop.2016.0140. Epub 2017 Mar 29. J Ocul Pharmacol Ther. 2017. PMID: 28355091 Review.
Cytomegalovirus (CMV) is a ubiquitous DNA herpes virus that causes significant morbidity and mortality in immunocompromised individuals. CMV retinitis is a potentially blinding manifestation of CMV infection that was commonly seen in advanced acquired immunodeficiency s …
Cytomegalovirus (CMV) is a ubiquitous DNA herpes virus that causes significant morbidity and mortality in immunocompromised individuals. CMV …
Asymmetric diabetic retinopathy.
Azad R, Sinha S, Nishant P. Azad R, et al. Indian J Ophthalmol. 2021 Nov;69(11):3026-3034. doi: 10.4103/ijo.IJO_1525_21. Indian J Ophthalmol. 2021. PMID: 34708738 Free PMC article. Review.
Associated factors can be divided into (i) vascular: carotid obstructive disease, ocular ischemic syndrome, and retinal vascular diseases; (ii) Inflammatory: uveitis, endophthalmitis, and Fuchs' heterochromic cyclitis; (iii) degenerative: posterior vitreous detachme …
Associated factors can be divided into (i) vascular: carotid obstructive disease, ocular ischemic syndrome, and retinal vascul …
Pachychoroid disease.
Cheung CMG, Lee WK, Koizumi H, Dansingani K, Lai TYY, Freund KB. Cheung CMG, et al. Eye (Lond). 2019 Jan;33(1):14-33. doi: 10.1038/s41433-018-0158-4. Epub 2018 Jul 11. Eye (Lond). 2019. PMID: 29995841 Free PMC article. Review.
Pachychoroid is a relatively novel concept describing a phenotype characterized by attenuation of the choriocapillaris overlying dilated choroidal veins, and associated with progressive retinal pigment epithelium dysfunction and neovascularization. The emphasis in defining …
Pachychoroid is a relatively novel concept describing a phenotype characterized by attenuation of the choriocapillaris overlying dilated cho …
Mitochondrial Disorder: Kearns-Sayre Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:161-162. doi: 10.1007/978-3-319-95046-4_30. Adv Exp Med Biol. 2018. PMID: 30578503 Review.
Mitochondrial diseases are multisystem disorders: anemia, myopathy, lactic acidosis, CNS abnormality, endocrine abnormalities, renal disease, sensorineural deafness, and retinal involvement. The clinical abnormalities are heterogeneous, and they usually begin in childhood. …
Mitochondrial diseases are multisystem disorders: anemia, myopathy, lactic acidosis, CNS abnormality, endocrine abnormalities, renal disease …
The Role of Inflammation in Diabetic Retinopathy.
Forrester JV, Kuffova L, Delibegovic M. Forrester JV, et al. Front Immunol. 2020 Nov 6;11:583687. doi: 10.3389/fimmu.2020.583687. eCollection 2020. Front Immunol. 2020. PMID: 33240272 Free PMC article. Review.
However, many of the clinical features of DR are late events and reflect the nature of the retinal architecture and its cellular composition. Retinal microvascular disease is, in fact, an early event pathogenetically, induced by low grade, persistent leukocyte activ …
However, many of the clinical features of DR are late events and reflect the nature of the retinal architecture and its cellular comp …
Retinitis pigmentosa.
Hamel C. Hamel C. Orphanet J Rare Dis. 2006 Oct 11;1:40. doi: 10.1186/1750-1172-1-40. Orphanet J Rare Dis. 2006. PMID: 17032466 Free PMC article. Review.
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal pigment deposits visible on fundus examination. ...In some cases, the clinical presentation is a cone-rod dystrophy, in which the dec …
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retin …
Genotype-phenotype correlates in Joubert syndrome: A review.
Gana S, Serpieri V, Valente EM. Gana S, et al. Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):72-88. doi: 10.1002/ajmg.c.31963. Epub 2022 Mar 3. Am J Med Genet C Semin Med Genet. 2022. PMID: 35238134 Free PMC article. Review.
Joubert syndrome (JS) is a genetically heterogeneous primary ciliopathy characterized by a pathognomonic cerebellar and brainstem malformation, the "molar tooth sign," and variable organ involvement. ...On the other hand, individuals with causal variants in the CEP290 or A …
Joubert syndrome (JS) is a genetically heterogeneous primary ciliopathy characterized by a pathognomonic cerebellar and brainstem mal …
Dandy-Walker Malformation.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B38-B41. doi: 10.1016/j.ajog.2020.08.184. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168220 Review. No abstract available.
2,498 results