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

Year Number of Results
1952 1
1960 1
1961 2
1965 1
1966 3
1967 3
1968 7
1969 7
1970 15
1971 14
1972 16
1973 9
1974 18
1975 12
1976 11
1977 12
1978 13
1979 21
1980 17
1981 21
1982 15
1983 23
1984 18
1985 22
1986 24
1987 27
1988 16
1989 30
1990 36
1991 47
1992 50
1993 45
1994 49
1995 35
1996 41
1997 48
1998 58
1999 77
2000 71
2001 88
2002 80
2003 77
2004 92
2005 102
2006 85
2007 114
2008 132
2009 149
2010 163
2011 157
2012 178
2013 192
2014 192
2015 170
2016 183
2017 222
2018 191
2019 162
2020 13
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Search Results

3,334 results
Results by year
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Page 1
Genetics of reflex seizures and epilepsies in humans and animals.
Italiano D, Striano P, Russo E, Leo A, Spina E, Zara F, Striano S, Gambardella A, Labate A, Gasparini S, Lamberti M, De Sarro G, Aguglia U, Ferlazzo E. Italiano D, et al. Epilepsy Res. 2016 Mar;121:47-54. doi: 10.1016/j.eplepsyres.2016.01.010. Epub 2016 Feb 2. Epilepsy Res. 2016. PMID: 26875109 Review.
The Influence of Vaccine on Febrile Seizure.
Li X, Lin Y, Yao G, Wang Y. Li X, et al. Curr Neuropharmacol. 2018;16(1):59-65. doi: 10.2174/1570159X15666170726115639. Curr Neuropharmacol. 2018. PMID: 28745219 Free PMC article. Review.
Genetic literacy series: genetic epilepsy with febrile seizures plus.
Myers KA, Scheffer IE, Berkovic SF; ILAE Genetics Commission. Myers KA, et al. Epileptic Disord. 2018 Aug 1;20(4):232-238. doi: 10.1684/epd.2018.0985. Epileptic Disord. 2018. PMID: 30078767 Free article. Review.
Genetic effects on sleep/wake variation of seizures.
Winawer MR, Shih J, Beck ES, Hunter JE, Epstein MP; EPGP Investigators. Winawer MR, et al. Epilepsia. 2016 Apr;57(4):557-65. doi: 10.1111/epi.13330. Epub 2016 Mar 6. Epilepsia. 2016. PMID: 26948972 Free PMC article. Clinical Trial.
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Trump N, McTague A, Brittain H, Papandreou A, Meyer E, Ngoh A, Palmer R, Morrogh D, Boustred C, Hurst JA, Jenkins L, Kurian MA, Scott RH. Trump N, et al. J Med Genet. 2016 May;53(5):310-7. doi: 10.1136/jmedgenet-2015-103263. Epub 2016 Mar 18. J Med Genet. 2016. PMID: 26993267 Free PMC article.
Severe neonatal seizures: From molecular diagnosis to precision therapy?
Milh M, Cacciagli P, Ravix C, Badens C, L├ępine A, Villeneuve N, Villard L. Milh M, et al. Rev Neurol (Paris). 2016 Mar;172(3):171-3. doi: 10.1016/j.neurol.2016.02.005. Epub 2016 Mar 15. Rev Neurol (Paris). 2016. PMID: 26993565 Review.
Parental Mosaicism in "De Novo" Epileptic Encephalopathies.
Myers CT, Hollingsworth G, Muir AM, Schneider AL, Thuesmunn Z, Knupp A, King C, Lacroix A, Mehaffey MG, Berkovic SF, Carvill GL, Sadleir LG, Scheffer IE, Mefford HC. Myers CT, et al. N Engl J Med. 2018 Apr 26;378(17):1646-1648. doi: 10.1056/NEJMc1714579. N Engl J Med. 2018. PMID: 29694806 Free PMC article. No abstract available.
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