Syndroom van Dravet (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Syndroom van Dravet" in Dutch language version.

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archive.today

(en) Dravet Syndrome Foundation, Diagnostic criteria. Gearchiveerd op 17 maart 2015. Geraadpleegd op 17 maart 2015.

doi.org

(en) Dravet C (2011). The core Dravet syndrome phenotype. Epilepsia 52: 3–9. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.02994.x.
(en) Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (2009). ParentalSCN1Amutation mosaicism in familial Dravet syndrome. Clinical Genetics 76 (4): 398–403. ISSN: 0009-9163. DOI: 10.1111/j.1399-0004.2009.01208.x.
(en) Granata T (2011). Comprehensive care of children with Dravet syndrome. Epilepsia 52: 90–94. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.03011.x.
(en) Hurst DL (1990). Epidemiology of Severe Myoclonic Epilepsy of Infancy. Epilepsia 31 (4): 397–400. ISSN: 0013-9580. DOI: 10.1111/j.1528-1157.1990.tb05494.x.

nih.gov

ncbi.nlm.nih.gov

(en) Miller IO, Sotero de Menezes MA (1993). GeneReviews®. University of Washington, Seattle, Seattle (WA).

wiley.com

onlinelibrary.wiley.com

(en) Dravet C (2011). The core Dravet syndrome phenotype. Epilepsia 52: 3–9. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.02994.x.
(en) Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (2009). ParentalSCN1Amutation mosaicism in familial Dravet syndrome. Clinical Genetics 76 (4): 398–403. ISSN: 0009-9163. DOI: 10.1111/j.1399-0004.2009.01208.x.
(en) Granata T (2011). Comprehensive care of children with Dravet syndrome. Epilepsia 52: 90–94. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.03011.x.
(en) Hurst DL (1990). Epidemiology of Severe Myoclonic Epilepsy of Infancy. Epilepsia 31 (4): 397–400. ISSN: 0013-9580. DOI: 10.1111/j.1528-1157.1990.tb05494.x.

worldcat.org

(en) Shorvon SD, Guerrini R, Cook M, Lhatoo SD (2013). Oxford textbook of epilepsy and epileptic seizures. Oxford University Press, Oxford, p. 13. ISBN 9780191640957.
(en) Dravet C (2011). The core Dravet syndrome phenotype. Epilepsia 52: 3–9. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.02994.x.
(en) Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (2009). ParentalSCN1Amutation mosaicism in familial Dravet syndrome. Clinical Genetics 76 (4): 398–403. ISSN: 0009-9163. DOI: 10.1111/j.1399-0004.2009.01208.x.
(en) Granata T (2011). Comprehensive care of children with Dravet syndrome. Epilepsia 52: 90–94. ISSN: 0013-9580. DOI: 10.1111/j.1528-1167.2011.03011.x.
(en) Hurst DL (1990). Epidemiology of Severe Myoclonic Epilepsy of Infancy. Epilepsia 31 (4): 397–400. ISSN: 0013-9580. DOI: 10.1111/j.1528-1157.1990.tb05494.x.