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

Year Number of Results
1953 1
1954 1
1956 1
1958 2
1961 1
1962 3
1964 3
1965 5
1966 8
1967 18
1968 14
1969 31
1970 26
1971 25
1972 30
1973 20
1974 29
1975 15
1976 20
1977 25
1978 20
1979 23
1980 19
1981 25
1982 48
1983 22
1984 19
1985 36
1986 20
1987 25
1988 47
1989 54
1990 67
1991 79
1992 90
1993 70
1994 99
1995 103
1996 98
1997 81
1998 128
1999 94
2000 121
2001 110
2002 118
2003 116
2004 99
2005 115
2006 141
2007 137
2008 159
2009 136
2010 177
2011 197
2012 204
2013 210
2014 224
2015 189
2016 192
2017 173
2018 208
2019 203
2020 253
2021 237
2022 248
2023 258
2024 73

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5,387 results

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Page 1
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.
Genes and mutations causing retinitis pigmentosa.
Daiger SP, Sullivan LS, Bowne SJ. Daiger SP, et al. Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19. Clin Genet. 2013. PMID: 23701314 Free PMC article. Review.
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH. Koyanagi Y, et al. J Med Genet. 2019 Oct;56(10):662-670. doi: 10.1136/jmedgenet-2018-105691. Epub 2019 Jun 17. J Med Genet. 2019. PMID: 31213501
Retinitis pigmentosa.
Pagon RA. Pagon RA. Surv Ophthalmol. 1988 Nov-Dec;33(3):137-77. doi: 10.1016/0039-6257(88)90085-9. Surv Ophthalmol. 1988. PMID: 3068820 Review.
Genomic Landscape of Sporadic Retinitis Pigmentosa: Findings from 877 Spanish Cases.
Martin-Merida I, Avila-Fernandez A, Del Pozo-Valero M, Blanco-Kelly F, Zurita O, Perez-Carro R, Aguilera-Garcia D, Riveiro-Alvarez R, Arteche A, Trujillo-Tiebas MJ, Tahsin-Swafiri S, Rodriguez-Pinilla E, Lorda-Sanchez I, Garcia-Sandoval B, Corton M, Ayuso C. Martin-Merida I, et al. Ophthalmology. 2019 Aug;126(8):1181-1188. doi: 10.1016/j.ophtha.2019.03.018. Epub 2019 Mar 20. Ophthalmology. 2019. PMID: 30902645
Autosomal Dominant Retinitis Pigmentosa.
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:69-77. doi: 10.1007/978-3-319-95046-4_15. Adv Exp Med Biol. 2018. PMID: 30578488 Review.
Etiology of Retinitis Pigmentosa.
Breazzano MP, Grewal MR, Tsang SH, Chen RWS. Breazzano MP, et al. Methods Mol Biol. 2023;2560:15-30. doi: 10.1007/978-1-0716-2651-1_2. Methods Mol Biol. 2023. PMID: 36481880
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus.
Galosi S, Edani BH, Martinelli S, Hansikova H, Eklund EA, Caputi C, Masuelli L, Corsten-Janssen N, Srour M, Oegema R, Bosch DGM, Ellis CA, Amlie-Wolf L, Accogli A, Atallah I, Averdunk L, Barañano KW, Bei R, Bagnasco I, Brusco A, Demarest S, Alaix AS, Di Bonaventura C, Distelmaier F, Elmslie F, Gan-Or Z, Good JM, Gripp K, Kamsteeg EJ, Macnamara E, Marcelis C, Mercier N, Peeden J, Pizzi S, Pannone L, Shinawi M, Toro C, Verbeek NE, Venkateswaran S, Wheeler PG, Zdrazilova L, Zhang R, Zorzi G, Guerrini R, Sessa WC, Lefeber DJ, Tartaglia M, Hamdan FF, Grabińska KA, Leuzzi V. Galosi S, et al. Brain. 2022 Mar 29;145(1):208-223. doi: 10.1093/brain/awab299. Brain. 2022. PMID: 34382076 Free PMC article.
5,387 results