Childhood Electroclinical Syndromes: A Diagnostic and Therapeutic Algorithm
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-014-1529-x.pdf
Reference23 articles.
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2. Engel Jr J. Report of the ILAE classification core group. Epilepsia. 2006;47:1558–68.
3. Blume WT, Luders HO, Mizrahi E, Tassinari C, van Emde Boas W, Engel Jr J. Glossary of descriptive terminology for ictal semiology: report of the ILAE task force on classification and terminology. Epilepsia. 2001;42:1212–8.
4. Soldovieri MV, Boutry-Kryza N, Milh M, Doummar D, Heron B, Bourel E, et al. Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. Hum Mutat. 2014;35:356–67.
5. Djemie T, Weckhuysen S, Holmgren P, Hardies K, Van Dyck T, Hendrickx R, et al. PRRT2 mutations: exploring the phenotypical boundaries. J Neurol Neurosurg Psychiatry. 2014;85:462–5.
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1. Updates on Pediatric Genetic Epileptic Encephalopathies: A Diagnostic Algorithmic Approach;Common Pediatric Diseases: an Updated Review;2022-04-13
2. An Update to Approach to the Childhood Electroclinical Syndromes;The Indian Journal of Pediatrics;2020-11-05
3. Editorial;The Indian Journal of Pediatrics;2014-08-08
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