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

Year Number of Results
1950 2
1954 3
1955 3
1957 1
1958 1
1959 3
1960 6
1961 3
1962 5
1963 4
1964 3
1965 9
1966 3
1967 3
1968 4
1969 3
1970 9
1971 7
1972 14
1973 8
1974 10
1975 13
1976 15
1977 10
1978 27
1979 19
1980 20
1981 15
1982 19
1983 28
1984 28
1985 26
1986 39
1987 40
1988 41
1989 42
1990 46
1991 40
1992 50
1993 51
1994 66
1995 58
1996 81
1997 74
1998 68
1999 75
2000 100
2001 87
2002 80
2003 91
2004 83
2005 82
2006 87
2007 102
2008 96
2009 83
2010 95
2011 115
2012 108
2013 122
2014 101
2015 124
2016 142
2017 135
2018 163
2019 146
2020 170
2021 184
2022 175
2023 160
2024 158
2025 183
2026 24

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Page 1
Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.
Oku K, Mizobuchi K, Mochizuki K, Tsunoda K, Matsushita I, Nagata T, Fujinami K, Suga A, Yoshitake K, Sakaguchi H, Hayashi T, Iwata T, Kondo H. Oku K, et al. Among authors: kondo h. Graefes Arch Clin Exp Ophthalmol. 2026 Jan 16. doi: 10.1007/s00417-025-07107-x. Online ahead of print. Graefes Arch Clin Exp Ophthalmol. 2026. PMID: 41543775 No abstract available.
3,877 results