سندرم دراوه (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "سندرم دراوه" in Persian language version.

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Lhatoo (2013). Simon Shorvon; Renzo Guerrini; Mark Cook; Samden D (eds.). Oxford textbook of epilepsy and epileptic seizures. Oxford [u.a.]: Oxford Univ. Press. p. 13. ISBN 978-0-19-965904-3.

Dravet, Charlotte (1 April 2011). "The core Dravet syndrome phenotype". Epilepsia. 52: 3–9. doi:10.1111/j.1528-1167.2011.02994.x.
Selmer, K.K.; Eriksson, A-S; Brandal, K.; Egeland, T.; Tallaksen, C.; Undlien, D.E. (1 October 2009). "Parental SCN1A mutation mosaicism in familial Dravet syndrome". Clinical Genetics. 76 (4): 398–403. doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951.
Granata, Tiziana (1 April 2011). "Comprehensive care of children with Dravet syndrome". Epilepsia. 52: 90–94. doi:10.1111/j.1528-1167.2011.03011.x.
Hurst, Daniel L. (August 1990). "Epidemiology of Severe Myoclonic Epilepsy of Infancy". Epilepsia. 31 (4): 397–400. doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145.
Yakoub, M; Dulac, O; Jambaqué, I; Chiron, C; Plouin, P (September 1992). "Early diagnosis of severe myoclonic epilepsy in infancy". Brain & development. 14 (5): 299–303. doi:10.1093/brain/aws151. PMID 1456383.

Selmer, K.K.; Eriksson, A-S; Brandal, K.; Egeland, T.; Tallaksen, C.; Undlien, D.E. (1 October 2009). "Parental SCN1A mutation mosaicism in familial Dravet syndrome". Clinical Genetics. 76 (4): 398–403. doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951.
Hurst, Daniel L. (August 1990). "Epidemiology of Severe Myoclonic Epilepsy of Infancy". Epilepsia. 31 (4): 397–400. doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145.
Yakoub, M; Dulac, O; Jambaqué, I; Chiron, C; Plouin, P (September 1992). "Early diagnosis of severe myoclonic epilepsy in infancy". Brain & development. 14 (5): 299–303. doi:10.1093/brain/aws151. PMID 1456383.