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Results by year

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

Year Number of Results
1946 3
1947 2
1948 7
1949 1
1951 20
1952 35
1953 42
1954 45
1955 31
1956 59
1957 75
1958 55
1959 54
1960 91
1961 101
1962 65
1963 5
1964 22
1965 233
1966 577
1967 792
1968 987
1969 1053
1970 1189
1971 1327
1972 1355
1973 1331
1974 1495
1975 1247
1976 1239
1977 1336
1978 1355
1979 1356
1980 1307
1981 1326
1982 1539
1983 1490
1984 1567
1985 1591
1986 1604
1987 1632
1988 1637
1989 1816
1990 2008
1991 2107
1992 2263
1993 2286
1994 2087
1995 2338
1996 2357
1997 2435
1998 2737
1999 2943
2000 2942
2001 3053
2002 3119
2003 3369
2004 3349
2005 3661
2006 4096
2007 4114
2008 4538
2009 4574
2010 5089
2011 5717
2012 5843
2013 6548
2014 6728
2015 6745
2016 6938
2017 7137
2018 7107
2019 7138
2020 7670
2021 7583
2022 7275
2023 6061
2024 1845

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Search Results

172,412 results

Results by year

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Page 1
Lyonization in ophthalmology.
Wuthisiri W, Lingao MD, Capasso JE, Levin AV. Wuthisiri W, et al. Curr Opin Ophthalmol. 2013 Sep;24(5):389-97. doi: 10.1097/ICU.0b013e3283641f91. Curr Opin Ophthalmol. 2013. PMID: 23892913 Review.
Myositis Mimics.
Michelle EH, Mammen AL. Michelle EH, et al. Curr Rheumatol Rep. 2015 Oct;17(10):63. doi: 10.1007/s11926-015-0541-0. Curr Rheumatol Rep. 2015. PMID: 26290112 Review.
Clinical diagnosis of genetic diseases.
Fong CT. Fong CT. Pediatr Ann. 1993 May;22(5):277-81. doi: 10.3928/0090-4481-19930501-07. Pediatr Ann. 1993. PMID: 8510994 Review. No abstract available.
Chronic tophaceous gout.
Bader H, Maghnam R. Bader H, et al. Pan Afr Med J. 2021 Nov 2;40:130. doi: 10.11604/pamj.2021.40.130.31983. eCollection 2021. Pan Afr Med J. 2021. PMID: 34909098 Free PMC article. No abstract available.
Prenatal genetic diagnosis. 3.
Milunsky A, Littlefield JW, Kanvfer JN, Kolodny EH, Shih VE, Atkins L. Milunsky A, et al. N Engl J Med. 1970 Dec 31;283(27):1498-504. doi: 10.1056/NEJM197012312832705. N Engl J Med. 1970. PMID: 4992307 Review. No abstract available.
Neuro-ophthalmic manifestations of the phakomatoses.
Douglas KAA, Douglas VP, Cestari DM. Douglas KAA, et al. Curr Opin Ophthalmol. 2019 Nov;30(6):434-442. doi: 10.1097/ICU.0000000000000609. Curr Opin Ophthalmol. 2019. PMID: 31464700 Review.
Inborn errors of metabolism.
Kolodny EH, Cable WJ. Kolodny EH, et al. Ann Neurol. 1982 Mar;11(3):221-32. doi: 10.1002/ana.410110302. Ann Neurol. 1982. PMID: 6807191 Review.
Hereditary jaundice.
[No authors listed] [No authors listed] Lancet. 1978 Oct 28;2(8096):926-7. Lancet. 1978. PMID: 81933 No abstract available.
Preimplantation polar body diagnosis.
Verlinsky Y, Kuliev A. Verlinsky Y, et al. Biochem Mol Med. 1996 Jun;58(1):13-7. doi: 10.1006/bmme.1996.0026. Biochem Mol Med. 1996. PMID: 8809340 Review.
172,412 results
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