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

Year Number of Results
1990 1
1992 1
1993 1
1994 1
1996 1
1997 1
1998 2
1999 2
2000 1
2001 3
2002 1
2003 4
2004 2
2005 3
2006 2
2007 1
2008 1
2009 2
2010 1
2011 1
2012 2
2013 2
2019 1
2022 1
2024 0

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Related Articles by Review for PMID: 11488881

36 results

Results by year

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Page 1
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
Singh R, Andermann E, Whitehouse WP, Harvey AS, Keene DL, Seni MH, Crossland KM, Andermann F, Berkovic SF, Scheffer IE. Singh R, et al. Epilepsia. 2001 Jul;42(7):837-44. doi: 10.1046/j.1528-1157.2001.042007837.x. Epilepsia. 2001. PMID: 11488881 Free article.
Myoclonic-astatic epilepsy.
Doose H. Doose H. Epilepsy Res Suppl. 1992;6:163-8. Epilepsy Res Suppl. 1992. PMID: 1418479 Review.
SCN1A Seizure Disorders.
Miller IO, Sotero de Menezes MA. Miller IO, et al. 2007 Nov 29 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Nov 29 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301494 Free Books & Documents. Review.
Clinical spectrum of SCN1A mutations.
Gambardella A, Marini C. Gambardella A, et al. Epilepsia. 2009 May;50 Suppl 5:20-3. doi: 10.1111/j.1528-1167.2009.02115.x. Epilepsia. 2009. PMID: 19469841 Free article. Review.
36 results