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2. Additional information regarding "Dravet syndrome: inroads into understanding epileptic encephalopathies". Kobayashi K; Ohtsuka Y; Ohmori I J Pediatr; 2012 Mar; 160(3):532-3. PubMed ID: 22226577 [No Abstract] [Full Text] [Related]
3. Dravet syndrome history. Dravet C Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():1-6. PubMed ID: 21504424 [TBL] [Abstract][Full Text] [Related]
4. Severe myoclonic epilepsy in infancy (Dravet syndrome) 30 years later. Dravet C; Bureau M; Dalla Bernardina B; Guerrini R Epilepsia; 2011 Apr; 52 Suppl 2():1-2. PubMed ID: 21463271 [No Abstract] [Full Text] [Related]
5. Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene. Verbeek NE; van Kempen M; Gunning WB; Renier WO; Westland B; Lindhout D; Brilstra EH Epilepsia; 2011 Apr; 52(4):e23-5. PubMed ID: 21371021 [TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of Dravet syndrome. De Jonghe P Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():7-10. PubMed ID: 21504425 [TBL] [Abstract][Full Text] [Related]
12. A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3. Mastrangelo M; Mei D; Cesario S; Fioriello F; Bernardini L; Brinciotti M; Guerrini R; Leuzzi V Parkinsonism Relat Disord; 2019 Nov; 68():1-3. PubMed ID: 31621611 [No Abstract] [Full Text] [Related]
13. Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults. Jansen FE; Sadleir LG; Harkin LA; Vadlamudi L; McMahon JM; Mulley JC; Scheffer IE; Berkovic SF Neurology; 2006 Dec; 67(12):2224-6. PubMed ID: 17190949 [TBL] [Abstract][Full Text] [Related]
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