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Results by year

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

Year Number of Results
1945 1
1946 1
1947 2
1949 2
1955 1
1956 1
1957 1
1959 6
1960 5
1961 13
1962 6
1965 24
1966 49
1967 45
1968 68
1969 58
1970 97
1971 94
1972 82
1973 76
1974 144
1975 94
1976 88
1977 89
1978 64
1979 31
1980 33
1981 38
1982 21
1983 45
1984 41
1985 23
1986 53
1987 39
1988 24
1989 24
1990 33
1991 49
1992 39
1993 44
1994 47
1995 50
1996 27
1997 51
1998 68
1999 84
2000 114
2001 95
2002 75
2003 55
2004 48
2005 42
2006 62
2007 87
2008 77
2009 74
2010 130
2011 111
2012 111
2013 100
2014 94
2015 91
2016 134
2017 140
2018 108
2019 101
2020 98
2021 112
2022 88
2023 69
2024 42

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3,991 results

Results by year

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Page 1
Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy.
Testa F, Carreño E, van den Born LI, Melillo P, Perea-Romero I, Di Iorio V, Risca G, Iodice CM, Pennings RJE, Karali M, Banfi S, Auricchio A, Galimberti S, Ayuso C, Simonelli F. Testa F, et al. Invest Ophthalmol Vis Sci. 2024 Jun 3;65(6):25. doi: 10.1167/iovs.65.6.25. Invest Ophthalmol Vis Sci. 2024. PMID: 38884554 Free PMC article.
Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire.
Parekh B, Duncan JL, Samarakoon L, Melia M, Abalem MF, Andrews CA, Audo I, Ayala AR, Bradley C, Cheetham JK, Dagnelie G, Durham TA, Huckfeldt RM, Lacy GD, Malbin B, Michaelides M, Musch DC, Peck-Dimit N, Stingl K, Weng CY, Zmejkoski AZ, Jayasundera KT; Foundation Fighting Blindness Clinical Consortium Investigator Group. Parekh B, et al. Invest Ophthalmol Vis Sci. 2024 Jun 3;65(6):5. doi: 10.1167/iovs.65.6.5. Invest Ophthalmol Vis Sci. 2024. PMID: 38833260 Free PMC article.
Syndromic Retinitis Pigmentosa: A 15-Patient Study.
Holanda IP, Rim PHH, Rare Genomes Project Consortium, Guaragna MS, Gil-da-Silva-Lopes VL, Steiner CE. Holanda IP, et al. Genes (Basel). 2024 Apr 20;15(4):516. doi: 10.3390/genes15040516. Genes (Basel). 2024. PMID: 38674450 Free PMC article.
Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.
Gao B, Jiang Y, Han M, Ji X, Zhang D, Wu L, Gao X, Huang S, Zhao C, Su Y, Yang S, Zhang X, Liu N, Han L, Wang L, Ren L, Yang J, Wu J, Yuan Y, Dai P. Gao B, et al. J Mol Diagn. 2024 Jul;26(7):638-651. doi: 10.1016/j.jmoldx.2024.04.002. Epub 2024 Apr 23. J Mol Diagn. 2024. PMID: 38663495 Free article.
3,991 results
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