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Results by year

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

Year Number of Results
1963 2
1964 2
1965 3
1966 1
1967 8
1968 12
1969 17
1970 15
1971 12
1972 24
1973 14
1974 10
1975 12
1976 10
1977 17
1978 15
1979 12
1980 8
1981 9
1982 11
1983 10
1984 12
1985 19
1986 9
1987 14
1988 23
1989 31
1990 36
1991 43
1992 46
1993 68
1994 70
1995 87
1996 64
1997 95
1998 94
1999 137
2000 112
2001 120
2002 131
2003 149
2004 162
2005 138
2006 152
2007 182
2008 142
2009 147
2010 179
2011 170
2012 202
2013 194
2014 195
2015 190
2016 225
2017 182
2018 175
2019 157
2020 188
2021 177
2022 144
2023 124
2024 50

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Search Results

4,638 results

Results by year

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Page 1
Vascular dementia.
O'Brien JT, Thomas A. O'Brien JT, et al. Lancet. 2015 Oct 24;386(10004):1698-706. doi: 10.1016/S0140-6736(15)00463-8. Lancet. 2015. PMID: 26595643 Review.
Adulthood leukodystrophies.
Köhler W, Curiel J, Vanderver A. Köhler W, et al. Nat Rev Neurol. 2018 Feb;14(2):94-105. doi: 10.1038/nrneurol.2017.175. Epub 2018 Jan 5. Nat Rev Neurol. 2018. PMID: 29302065 Review.
White Matter Diseases with Radiologic-Pathologic Correlation.
Sarbu N, Shih RY, Jones RV, Horkayne-Szakaly I, Oleaga L, Smirniotopoulos JG. Sarbu N, et al. Radiographics. 2016 Sep-Oct;36(5):1426-47. doi: 10.1148/rg.2016160031. Radiographics. 2016. PMID: 27618323 Updated. Review.
Mechanisms of cognitive dysfunction in CKD.
Viggiano D, Wagner CA, Martino G, Nedergaard M, Zoccali C, Unwin R, Capasso G. Viggiano D, et al. Nat Rev Nephrol. 2020 Aug;16(8):452-469. doi: 10.1038/s41581-020-0266-9. Epub 2020 Mar 31. Nat Rev Nephrol. 2020. PMID: 32235904 Review.
Case definition and classification of leukodystrophies and leukoencephalopathies.
Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, Garbern J, Eichler F, Labauge P, Aubourg P, Rodriguez D, Patterson MC, Van Hove JL, Schmidt J, Wolf NI, Boespflug-Tanguy O, Schiffmann R, van der Knaap MS; GLIA Consortium. Vanderver A, et al. Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29. Mol Genet Metab. 2015. PMID: 25649058 Free PMC article. Review.
In addition, a separate set of disorders with heritable white matter abnormalities but not meeting criteria for leukodystrophy, due to presumed primary neuronal involvement and prominent systemic manifestations, was classified as genetic leukoencephalopathies (gLE). INTERP …
In addition, a separate set of disorders with heritable white matter abnormalities but not meeting criteria for leukodystrophy, due to presu …
4,638 results