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Year | Number of Results |
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2007 | 1 |
2014 | 2 |
2017 | 1 |
2024 | 0 |
PubMed (cited) for id: 619317
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Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
Neurology. 2017 Sep 5;89(10):1035-1042. doi: 10.1212/WNL.0000000000004331. Epub 2017 Aug 9.
Neurology. 2017.
PMID: 28794249
Free PMC article.
Infantile epileptic encephalopathy with a hyperkinetic movement disorder and hand stereotypies associated with a novel SCN1A mutation.
Ohashi T, Akasaka N, Kobayashi Y, Magara S, Kawashima H, Matsumoto N, Saitsu H, Tohyama J.
Ohashi T, et al.
Epileptic Disord. 2014 Jun;16(2):208-12. doi: 10.1684/epd.2014.0649.
Epileptic Disord. 2014.
PMID: 24776920
Free article.
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Sleep abnormalities in children with Dravet syndrome.
Dhamija R, Erickson MK, St Louis EK, Wirrell E, Kotagal S.
Dhamija R, et al.
Pediatr Neurol. 2014 May;50(5):474-8. doi: 10.1016/j.pediatrneurol.2014.01.017. Epub 2014 Jan 7.
Pediatr Neurol. 2014.
PMID: 24656210
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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.
Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002.
Brain. 2007.
PMID: 17347258
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