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Results by year

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

Year Number of Results
2004 2
2005 2
2006 3
2007 3
2008 3
2009 2
2010 3
2011 2
2012 8
2013 5
2014 7
2015 11
2016 12
2017 12
2018 4
2019 2
2021 1
2023 1
2024 0

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Similar articles for PMID: 28762608

73 results

Results by year

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Page 1
Truncating mutation in CSNK2B and myoclonic epilepsy.
Sakaguchi Y, Uehara T, Suzuki H, Kosaki K, Takenouchi T. Sakaguchi Y, et al. Hum Mutat. 2017 Nov;38(11):1611-1612. doi: 10.1002/humu.23307. Epub 2017 Sep 14. Hum Mutat. 2017. PMID: 28762608 No abstract available.
Is epilepsy the cause of comorbidities in Dravet syndrome?
Gataullina S, Dulac O. Gataullina S, et al. Dev Med Child Neurol. 2018 Jan;60(1):8. doi: 10.1111/dmcn.13613. Epub 2017 Nov 10. Dev Med Child Neurol. 2018. PMID: 29124748 Free article. No abstract available.
Dravet syndrome, what is new?
Al-Baradie RS. Al-Baradie RS. Neurosciences (Riyadh). 2013 Jan;18(1):11-7. Neurosciences (Riyadh). 2013. PMID: 23291792 Review.
Dravet syndrome: a genetic epileptic disorder.
Akiyama M, Kobayashi K, Ohtsuka Y. Akiyama M, et al. Acta Med Okayama. 2012;66(5):369-76. doi: 10.18926/AMO/48961. Acta Med Okayama. 2012. PMID: 23093055 Free article. Review.
The multiple faces of Dravet syndrome.
Andrade DM. Andrade DM. Dev Med Child Neurol. 2014 Jan;56(1):10-1. doi: 10.1111/dmcn.12332. Dev Med Child Neurol. 2014. PMID: 24328832 Free article. No abstract available.
[Vaccine encephalopathy: a myth collapses?].
Kahane P, Arzimanoglou A. Kahane P, et al. Presse Med. 2007 Oct;36(10 Pt 1):1339-40. doi: 10.1016/j.lpm.2007.05.025. Epub 2007 Jul 30. Presse Med. 2007. PMID: 17659861 French. No abstract available.
73 results