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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2017 | 1 |
2019 | 1 |
2020 | 2 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
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Genetic Diagnosis for 64 Patients with Inherited Retinal Disease.
Genes (Basel). 2022 Dec 26;14(1):74. doi: 10.3390/genes14010074.
Genes (Basel). 2022.
PMID: 36672815
Free PMC article.
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1.
Radojevic B, Jones K, Klein M, Mauro-Herrera M, Kingsley R, Birch DG, Bennett LD.
Radojevic B, et al.
Ophthalmic Genet. 2021 Feb;42(1):15-22. doi: 10.1080/13816810.2020.1832532. Epub 2020 Oct 14.
Ophthalmic Genet. 2021.
PMID: 33465333
Free PMC article.
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Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations.
Bennett LD, Metz G, Klein M, Locke KG, Khwaja A, Birch DG.
Bennett LD, et al.
Invest Ophthalmol Vis Sci. 2019 Mar 1;60(4):1122-1131. doi: 10.1167/iovs.18-25473.
Invest Ophthalmol Vis Sci. 2019.
PMID: 30901388
Free PMC article.
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Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1).
Bennett LD, Klein M, John FT, Radojevic B, Jones K, Birch DG.
Bennett LD, et al.
Transl Vis Sci Technol. 2020 Apr 23;9(5):14. doi: 10.1167/tvst.9.5.14. eCollection 2020 Apr.
Transl Vis Sci Technol. 2020.
PMID: 32821486
Free PMC article.
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Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa.
Bennett LD, Klein M, Locke KG, Kiser K, Birch DG.
Bennett LD, et al.
Transl Vis Sci Technol. 2017 Aug 9;6(4):15. doi: 10.1167/tvst.6.4.15. eCollection 2017 Jul.
Transl Vis Sci Technol. 2017.
PMID: 28798898
Free PMC article.
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