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

Year Number of Results
1969 1
1972 1
1973 1
1974 1
1975 1
1976 2
1977 2
1979 1
1980 6
1982 4
1984 3
1985 3
1986 5
1987 3
1988 10
1989 2
1990 4
1991 8
1992 8
1993 13
1994 9
1995 5
1996 11
1997 7
1998 12
1999 7
2000 4
2001 8
2002 4
2003 8
2004 12
2005 12
2006 3
2007 5
2008 4
2009 4
2010 4
2011 4
2012 4
2013 7
2014 4
2015 8
2016 3
2017 2
2018 3
2019 3
2020 2
2021 2
2022 0
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Article attribute
Article type
Publication date

Search Results

230 results
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Page 1
The spectrum of SCN1A-related infantile epileptic encephalopathies.
Harkin LA, McMahon JM, Iona X, Dibbens L, Pelekanos JT, Zuberi SM, Sadleir LG, Andermann E, Gill D, Farrell K, Connolly M, Stanley T, Harbord M, Andermann F, Wang J, Batish SD, Jones JG, Seltzer WK, Gardner A; Infantile Epileptic Encephalopathy Referral Consortium, Sutherland G, Berkovic SF, Mulley JC, Scheffer IE. Harkin LA, et al. Among authors: andermann e. Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002. Brain. 2007. PMID: 17347258
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.
Courage C, Oliver KL, Park EJ, Cameron JM, Grabińska KA, Muona M, Canafoglia L, Gambardella A, Said E, Afawi Z, Baykan B, Brandt C, di Bonaventura C, Chew HB, Criscuolo C, Dibbens LM, Castellotti B, Riguzzi P, Labate A, Filla A, Giallonardo AT, Berecki G, Jackson CB, Joensuu T, Damiano JA, Kivity S, Korczyn A, Palotie A, Striano P, Uccellini D, Giuliano L, Andermann E, Scheffer IE, Michelucci R, Bahlo M, Franceschetti S, Sessa WC, Berkovic SF, Lehesjoki AE. Courage C, et al. Among authors: andermann e. Am J Hum Genet. 2021 Apr 1;108(4):722-738. doi: 10.1016/j.ajhg.2021.03.013. Am J Hum Genet. 2021. PMID: 33798445 Free PMC article.
Progressive Myoclonus Epilepsy, Lafora Type.
Jansen AC, Andermann E. Jansen AC, et al. Among authors: andermann e. 2007 Dec 28 [updated 2019 Feb 21]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2007 Dec 28 [updated 2019 Feb 21]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301563 Free Books & Documents. Review.
Benign mesial temporal lobe epilepsy.
Labate A, Gambardella A, Andermann E, Aguglia U, Cendes F, Berkovic SF, Andermann F. Labate A, et al. Among authors: andermann e. Nat Rev Neurol. 2011 Apr;7(4):237-40. doi: 10.1038/nrneurol.2010.212. Epub 2011 Jan 25. Nat Rev Neurol. 2011. PMID: 21263461 Review.
Action Myoclonus – Renal Failure Syndrome.
Amrom D, Andermann F, Andermann E. Amrom D, et al. Among authors: andermann e. 2015 Dec 17. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2015 Dec 17. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 26677510 Free Books & Documents. Review.
Genetics of the polymicrogyria syndromes.
Jansen A, Andermann E. Jansen A, et al. Among authors: andermann e. J Med Genet. 2005 May;42(5):369-78. doi: 10.1136/jmg.2004.023952. J Med Genet. 2005. PMID: 15863665 Free PMC article. Review.
X-linked malformations of neuronal migration.
Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, Walsh CA, Truwit CL. Dobyns WB, et al. Among authors: andermann e. Neurology. 1996 Aug;47(2):331-9. doi: 10.1212/wnl.47.2.331. Neurology. 1996. PMID: 8757001 Review.
Kufs disease: clinical features and forms.
Berkovic SF, Andermann F, Andermann E, Carpenter S, Wolfe L. Berkovic SF, et al. Among authors: andermann e. Am J Med Genet Suppl. 1988;5:105-9. doi: 10.1002/ajmg.1320310614. Am J Med Genet Suppl. 1988. PMID: 3146309 Review.
230 results