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

Year Number of Results
2006 1
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2013 2
2014 2
2015 1
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2020 4
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2023 17
2024 6

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Quoted phrase not found in phrase index: "Retinal dystrophy with or without macular staphyloma"
Page 1
Stem cell therapy for inherited retinal diseases: a systematic review and meta-analysis.
Chen X, Xu N, Li J, Zhao M, Huang L. Chen X, et al. Stem Cell Res Ther. 2023 Oct 5;14(1):286. doi: 10.1186/s13287-023-03526-x. Stem Cell Res Ther. 2023. PMID: 37798796 Free PMC article. Review.
PURPOSE: Stem cell therapy is a promising therapeutic approach for inherited retinal diseases (IRDs). This study aims to quantitatively examine the effectiveness and safety of stem cell therapy for patients with IRDs, including retinitis pigmentosa and Stargardt disease (S …
PURPOSE: Stem cell therapy is a promising therapeutic approach for inherited retinal diseases (IRDs). This study aims to quantitative …
Retinitis Pigmentosa: Progress and Perspective.
Zhang Q. Zhang Q. Asia Pac J Ophthalmol (Phila). 2016 Jul-Aug;5(4):265-71. doi: 10.1097/APO.0000000000000227. Asia Pac J Ophthalmol (Phila). 2016. PMID: 27488069 Free article. Review.
Retinitis pigmentosa is the most common form of hereditary retinal degeneration causing blindness. Great progress has been made in the identification of the causative genes. ...
Retinitis pigmentosa is the most common form of hereditary retinal degeneration causing blindness. Great progress has been made in th …
β-Thalassemia and ocular implications: a systematic review.
Liaska A, Petrou P, Georgakopoulos CD, Diamanti R, Papaconstantinou D, Kanakis MG, Georgalas I. Liaska A, et al. BMC Ophthalmol. 2016 Jul 8;16:102. doi: 10.1186/s12886-016-0285-2. BMC Ophthalmol. 2016. PMID: 27390837 Free PMC article. Review.
Ocular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE), including peau d'orange, angioid streaks, pattern dystrophy-like changes, and optic disc drusen are a consistent finding in seven studies. ...These changes increase with duration or severity of t …
Ocular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE), including peau d'orange, angioid streaks, pattern dystrophy …
Topical Treatment for Retinal Degenerative Pathologies: A Systematic Review.
Samoilă L, Voștinaru O, Dinte E, Bodoki AE, Iacob BC, Bodoki E, Samoilă O. Samoilă L, et al. Int J Mol Sci. 2023 Apr 28;24(9):8045. doi: 10.3390/ijms24098045. Int J Mol Sci. 2023. PMID: 37175752 Free PMC article. Review.
Database search returned 102 clinical studies, focused on topical treatment for age macular degeneration, macular edemas (in diabetic retinopathy, surgery related or in retinal dystrophies) or glaucoma. After the exclusion of low-powered studies and th …
Database search returned 102 clinical studies, focused on topical treatment for age macular degeneration, macular edemas (in d …
Neurological manifestations in mevalonate kinase deficiency: A systematic review.
Elhani I, Hentgen V, Grateau G, Georgin-Lavialle S. Elhani I, et al. Mol Genet Metab. 2022 Jun;136(2):85-93. doi: 10.1016/j.ymgme.2022.04.006. Epub 2022 Apr 30. Mol Genet Metab. 2022. PMID: 35525811 Review.
Serious involvements including ataxia and developmental delay were described less than 1% of patients but 22-31% of case reports. They consistently appeared in the first years of life. Retinal dystrophy was frequently reported (31%) in case reports. Other manifestat …
Serious involvements including ataxia and developmental delay were described less than 1% of patients but 22-31% of case reports. They consi …
The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic review.
Britten-Jones AC, Jin R, Gocuk SA, Cichello E, O'Hare F, Hickey DG, Edwards TL, Ayton LN. Britten-Jones AC, et al. Genet Med. 2022 Mar;24(3):521-534. doi: 10.1016/j.gim.2021.10.013. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906485 Free article. Review.
PURPOSE: This study aimed to systematically review and summarize gene therapy treatment for monogenic retinal and optic nerve diseases. METHODS: This review was prospectively registered (CRD42021229812). ...Study summaries and visual representations of safety and efficacy …
PURPOSE: This study aimed to systematically review and summarize gene therapy treatment for monogenic retinal and optic nerve disease …
Evidence Synthesis of Gene Therapy and Gene Editing from Different Disorders-Implications for Individuals with Rett Syndrome: A Systematic Review.
Singh J, Goodman-Vincent E, Santosh P. Singh J, et al. Int J Mol Sci. 2023 May 19;24(10):9023. doi: 10.3390/ijms24109023. Int J Mol Sci. 2023. PMID: 37240368 Free PMC article. Review.
This systematic review and thematic analysis critically evaluated gene therapy trials in amyotrophic lateral sclerosis, haemoglobinopathies, immunodeficiencies, leukodystrophies, lysosomal storage disorders and retinal dystrophies and extrapolated the key clinical f …
This systematic review and thematic analysis critically evaluated gene therapy trials in amyotrophic lateral sclerosis, haemoglobinopathies, …
Advances in Retinal Prosthetic Research: A Systematic Review of Engineering and Clinical Characteristics of Current Prosthetic Initiatives.
Cheng DL, Greenberg PB, Borton DA. Cheng DL, et al. Curr Eye Res. 2017 Mar;42(3):334-347. doi: 10.1080/02713683.2016.1270326. Epub 2017 Feb 26. Curr Eye Res. 2017. PMID: 28362177 Review.
To address these gaps, this systematic review examines worldwide advances in retinal prosthetic research, evaluates engineering characteristics and clinical progress of contemporary device initiatives, and identifies potential directions for future research in the field of …
To address these gaps, this systematic review examines worldwide advances in retinal prosthetic research, evaluates engineering chara …
Clinical and Genetic Features of NR2E3-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review.
Xiao S, Yi Z, Xiao X, Li S, Jia X, Lian P, Sun W, Wang P, Lu L, Zhang Q. Xiao S, et al. Genes (Basel). 2023 Jul 26;14(8):1525. doi: 10.3390/genes14081525. Genes (Basel). 2023. PMID: 37628579 Free PMC article.
(1) Background: NR2E3 encodes a nuclear receptor transcription factor that is considered to promote cell differentiation, affect retinal development, and regulate phototransduction in rods and cones. ...A systemic literature review indicated patients with ADRP presented be …
(1) Background: NR2E3 encodes a nuclear receptor transcription factor that is considered to promote cell differentiation, affect retinal …
55 results