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

Year Number of Results
1982 1
1996 1
1997 1
2007 1
2008 1
2012 1
2019 1
2021 3
2022 1
2023 1
2024 0

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11 results

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Page 1
Retinitis Pigmentosa: Review of Current Treatment.
Wang AL, Knight DK, Vu TT, Mehta MC. Wang AL, et al. Int Ophthalmol Clin. 2019 Winter;59(1):263-280. doi: 10.1097/IIO.0000000000000256. Int Ophthalmol Clin. 2019. PMID: 30585930 Review. No abstract available.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
Disease-causing sequence variants in CNGB1 lead to autosomal recessive rod-cone dystrophy/retinitis pigmentosa (RP). We herein present a comprehensive review and analysis of all previously reported CNGB1 sequence variants, and add 22 novel variants, thereby enlargin …
Disease-causing sequence variants in CNGB1 lead to autosomal recessive rod-cone dystrophy/retinitis pigmentosa (RP). We herein …
Diagnostic imaging in patients with retinitis pigmentosa.
Mitamura Y, Mitamura-Aizawa S, Nagasawa T, Katome T, Eguchi H, Naito T. Mitamura Y, et al. J Med Invest. 2012;59(1-2):1-11. doi: 10.2152/jmi.59.1. J Med Invest. 2012. PMID: 22449988 Free article. Review.
Retinitis pigmentosa (RP) is a progressive inherited retinal disease, and patients with RP have reduced visual function caused by a degeneration of the photoreceptors and retinal pigment epithelium (RPE). ...
Retinitis pigmentosa (RP) is a progressive inherited retinal disease, and patients with RP have reduced visual function caused …
Hearing loss in Africa: current genetic profile.
Adadey SM, Wonkam-Tingang E, Aboagye ET, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Hum Genet. 2022 Apr;141(3-4):505-517. doi: 10.1007/s00439-021-02376-y. Epub 2021 Oct 5. Hum Genet. 2022. PMID: 34609590 Free PMC article. Review.
The most common method used in these publications was targeted gene sequencing (n = 66/111; 59.5%), and only 13.5% (n = 15/111) used whole-exome sequencing. ...
The most common method used in these publications was targeted gene sequencing (n = 66/111; 59.5%), and only 13.5% (n = 15/111) used …
Stem-cell-based therapies for retinal degenerative diseases: Current challenges in the establishment of new treatment strategies.
Uyama H, Mandai M, Takahashi M. Uyama H, et al. Dev Growth Differ. 2021 Jan;63(1):59-71. doi: 10.1111/dgd.12704. Epub 2021 Jan 21. Dev Growth Differ. 2021. PMID: 33315237 Free PMC article. Review.
However, the treatment of degenerative retinal diseases, such as retinitis pigmentosa (RP) and age-related macular degeneration (AMD), continues to pose a significant challenge. ...
However, the treatment of degenerative retinal diseases, such as retinitis pigmentosa (RP) and age-related macular degeneratio …
[Complicated cataracts in various forms of retinitis pigmentosa. Type and incidence].
Auffarth GU, Tetz MR, Krastel H, Blankenagel A, Völcker HE. Auffarth GU, et al. Ophthalmologe. 1997 Sep;94(9):642-6. doi: 10.1007/s003470050175. Ophthalmologe. 1997. PMID: 9410231 Review. German.
PURPOSE: To study the incidence and types of cataract in retinitis pigmentosa (RP) and their variations among different forms of RP. ...
PURPOSE: To study the incidence and types of cataract in retinitis pigmentosa (RP) and their variations among different forms …
Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.
Sullivan LS, Daiger SP. Sullivan LS, et al. Mol Med Today. 1996 Sep;2(9):380-6. doi: 10.1016/s1357-4310(96)10037-x. Mol Med Today. 1996. PMID: 8885257 Review.
Rapid progress is being made in identifying the genetic causes of common, inherited retinal diseases, such as retinitis pigmentosa and macular degeneration, as well as some of the rare forms of retinal disease. Linkage studies of large families and candidate-gene sc …
Rapid progress is being made in identifying the genetic causes of common, inherited retinal diseases, such as retinitis pigmentosa …
Stargardt's disease and the ABCR gene.
Westerfeld C, Mukai S. Westerfeld C, et al. Semin Ophthalmol. 2008 Jan-Feb;23(1):59-65. doi: 10.1080/08820530701745249. Semin Ophthalmol. 2008. PMID: 18214793 Review.
Mutations in this gene have also been attributed to some cases of cone-rod dystrophy, retinitis pigmentosa, and age-related macular degeneration. The genetic and molecular pathways that produce Stargardt's disease will be discussed. ...
Mutations in this gene have also been attributed to some cases of cone-rod dystrophy, retinitis pigmentosa, and age-related ma …
[Advances on gene therapy for USH2A exon 13 related inherited retinal dystrophy].
Li WY, Sui RF. Li WY, et al. Zhonghua Yan Ke Za Zhi. 2023 Dec 11;59(12):1058-1064. doi: 10.3760/cma.j.cn112142-20231024-00169. Zhonghua Yan Ke Za Zhi. 2023. PMID: 38061908 Review. Chinese.
Biallelic pathogenic variants in the USH2A gene result in Usher syndrome type and non-syndromic retinitis pigmentosa, both of which entail the progressive loss of photoreceptors leading to blindness. ...
Biallelic pathogenic variants in the USH2A gene result in Usher syndrome type and non-syndromic retinitis pigmentosa, both of …
A selected review of retinal research and study.
Cohen J. Cohen J. Am J Optom Physiol Opt. 1982 Sep;59(9):738-50. doi: 10.1097/00006324-198209000-00006. Am J Optom Physiol Opt. 1982. PMID: 6753593 Review. No abstract available.
11 results