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Epilepsy

Free Subscription Articles published in Dev Med Child Neurol Retrieve available abstracts of 35 articles: HTML format Text format

Single Articles

November 2018
1. ALI S, Scheffer IE, Sadleir LG
   Efficacy of cannabinoids in paediatric epilepsy.
   Dev Med Child Neurol. 2018 Nov 6. doi: 10.1111/dmcn.14087.
   PubMed     Text format     Abstract available
   
   
   September 2018
2. SARTORI S, Nosadini M, Tessarin G, Boniver C, et al
   First-ever convulsive seizures in children presenting to the emergency department: risk factors for seizure recurrence and diagnosis of epilepsy.
   Dev Med Child Neurol. 2018 Sep 7. doi: 10.1111/dmcn.14015.
   PubMed     Text format     Abstract available
   
   
   August 2018
3. CORTES-SALADELAFONT E, Molero-Luis M, Cuadras D, Casado M, et al
   Gamma-aminobutyric acid levels in cerebrospinal fluid in neuropaediatric disorders.
   Dev Med Child Neurol. 2018;60:780-792.
   PubMed     Text format     Abstract available
   
   
   July 2018
4. DAN B
   Vagal nerve stimulation beyond epilepsy.
   Dev Med Child Neurol. 2018;60:634.
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   June 2018
5. KIRSCH AC, Zaccariello MJ
   Global development and adaptive functioning in children with epilepsy.
   Dev Med Child Neurol. 2018 Jun 21. doi: 10.1111/dmcn.13941.
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6. REILLY C, Atkinson P, Memon A, Jones C, et al
   Global development and adaptive behaviour in children with early-onset epilepsy: a population-based case-control study.
   Dev Med Child Neurol. 2018 Jun 3. doi: 10.1111/dmcn.13926.
   PubMed     Text format     Abstract available
   
   
   
7. CHIRON C
   Long-term pragmatic use of stiripentol for Dravet syndrome.
   Dev Med Child Neurol. 2018;60:535.
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8. MYERS KA, Lightfoot P, Patil SG, Cross JH, et al
   Stiripentol efficacy and safety in Dravet syndrome: a 12-year observational study.
   Dev Med Child Neurol. 2018;60:574-578.
   PubMed     Text format     Abstract available
   
   
   April 2018
9. DRAVET C
   Acute encephalopathy after febrile status epilepticus: an underdiagnosed, misunderstood complication of Dravet syndrome.
   Dev Med Child Neurol. 2018 Apr 14. doi: 10.1111/dmcn.13778.
   PubMed     Text format    
   
   
   
10. WRIGHT I
    Paediatric convulsive status epilepticus, epilepsy, and behavioural outcomes.
    Dev Med Child Neurol. 2018;60:338-339.
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11. AUVIN S
    A common language of seizures and epilepsies: International League Against Epilepsy 2017 classifications.
    Dev Med Child Neurol. 2018;60:329.
    PubMed     Text format    
    
    
    March 2018
12. TIAN X, Ye J, Zeng Q, Zhang J, et al
    The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome.
    Dev Med Child Neurol. 2018 Mar 24. doi: 10.1111/dmcn.13727.
    PubMed     Text format     Abstract available
    
    
    
13. VEGA C, Sanchez Fernandez I, Peters J, Thome-Souza MS, et al
    Response to clobazam in continuous spike-wave during sleep.
    Dev Med Child Neurol. 2018;60:283-289.
    PubMed     Text format     Abstract available
    
    
    February 2018
14. VILLALUZ MM, Lomax LB, Jadhav T, Cross JH, et al
    The ketogenic diet is effective for refractory epilepsy associated with acquired structural epileptic encephalopathy.
    Dev Med Child Neurol. 2018 Feb 16. doi: 10.1111/dmcn.13687.
    PubMed     Text format     Abstract available
    
    
    
15. ZUBERI SM
    Sleep, oxygen saturation, and seizures in Dravet syndrome.
    Dev Med Child Neurol. 2018;60:118.
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16. LICHENI SH, Mcmahon JM, Schneider AL, Davey MJ, et al
    Sleep problems in Dravet syndrome: a modifiable comorbidity.
    Dev Med Child Neurol. 2018;60:192-198.
    PubMed     Text format     Abstract available
    
    
    January 2018
17. LAGAE L, Brambilla I, Mingorance A, Gibson E, et al
    Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey.
    Dev Med Child Neurol. 2018;60:63-72.
    PubMed     Text format     Abstract available
    
    
    December 2017
18. VARADKAR S
    Continuous spike-wave during sleep: treating an epilepsy without seizures.
    Dev Med Child Neurol. 2017 Dec 28. doi: 10.1111/dmcn.13650.
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19. ROULET-PEREZ E, Mayor C
    Childhood epilepsy with centro-temporal spikes (rolandic epilepsy) and written language.
    Dev Med Child Neurol. 2017 Dec 21. doi: 10.1111/dmcn.13658.
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20. CURRIE NK, Lew AR, Palmer TM, Basu H, et al
    Reading comprehension difficulties in children with rolandic epilepsy.
    Dev Med Child Neurol. 2017 Dec 14. doi: 10.1111/dmcn.13628.
    PubMed     Text format     Abstract available
    
    
    
21. MARTINOS MM, Pujar S, Gillberg C, Cortina-Borja M, et al
    Long-term behavioural outcomes after paediatric convulsive status epilepticus: a population-based cohort study.
    Dev Med Child Neurol. 2017 Dec 10. doi: 10.1111/dmcn.13636.
    PubMed     Text format     Abstract available
    
    
    
22. RYDENHAG B
    Long-term effects of corpus callosotomy for therapy-resistant epileptic seizures.
    Dev Med Child Neurol. 2017 Dec 1. doi: 10.1111/dmcn.13639.
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    November 2017
23. TRIVISANO M, Specchio N
    Focal cortical dysplasia in genetic epilepsy: new insights from PCDH19-related epilepsy.
    Dev Med Child Neurol. 2017 Nov 14. doi: 10.1111/dmcn.13615.
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24. GATAULLINA S, Dulac O
    Is epilepsy the cause of comorbidities in Dravet syndrome?
    Dev Med Child Neurol. 2017 Nov 10. doi: 10.1111/dmcn.13613.
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25. STRASSER L, Downes M, Kung J, Cross JH, et al
    Prevalence and risk factors for autism spectrum disorder in epilepsy: a systematic review and meta-analysis.
    Dev Med Child Neurol. 2017 Nov 9. doi: 10.1111/dmcn.13598.
    PubMed     Text format     Abstract available
    
    
    October 2017
26. KURIAN M, Korff CM, Ranza E, Bernasconi A, et al
    Focal cortical malformations in children with early infantile epilepsy and PCDH19 mutations: case report.
    Dev Med Child Neurol. 2017 Oct 24. doi: 10.1111/dmcn.13595.
    PubMed     Text format     Abstract available
    
    
    
27. VOLLEBREGT AAM, Hoogeveen-Westerveld M, Kroos MA, Oussoren E, et al
    Genotype-phenotype relationship in mucopolysaccharidosis II: predictive power of IDS variants for the neuronopathic phenotype.
    Dev Med Child Neurol. 2017;59:1063-1070.
    PubMed     Text format     Abstract available
    
    
    September 2017
28. PILLI VK, Behen ME, Hu J, Xuan Y, et al
    Clinical and metabolic correlates of cerebral calcifications in Sturge-Weber syndrome.
    Dev Med Child Neurol. 2017;59:952-958.
    PubMed     Text format     Abstract available
    
    
    July 2017
29. DELOBEL-AYOUB M, Klapouszczak D, van Bakel MME, Horridge K, et al
    Prevalence and characteristics of autism spectrum disorders in children with cerebral palsy.
    Dev Med Child Neurol. 2017;59:738-742.
    PubMed     Text format     Abstract available
    
    
    June 2017
30. DOWNS J, Leonard H, Wong K, Newton N, et al
    Quantification of walking-based physical activity and sedentary time in individuals with Rett syndrome.
    Dev Med Child Neurol. 2017;59:605-611.
    PubMed     Text format     Abstract available
    
    
    
31. AMIN S, Lux A, Calder N, Laugharne M, et al
    Causes of mortality in individuals with tuberous sclerosis complex.
    Dev Med Child Neurol. 2017;59:612-617.
    PubMed     Text format     Abstract available
    
    
    January 2017
32. DAN B
    Gap junctions in epilepsy: for better or worse.
    Dev Med Child Neurol. 2017;59:4.
    PubMed     Text format    
    
    
    June 2016
33. HORRIDGE KA, Mcgarry K, Williams J, Whitlingum G, et al
    Prospective pilots of routine data capture by paediatricians in clinics and validation of the Disabilities Complexity Scale.
    Dev Med Child Neurol. 2016;58:581-8.
    PubMed     Text format     Abstract available
    
    
    
34. HORRIDGE KA, Harvey C, McGarry K, Williams J, et al
    Quantifying multifaceted needs captured at the point of care. Development of a Disabilities Terminology Set and Disabilities Complexity Scale.
    Dev Med Child Neurol. 2016;58:570-80.
    PubMed     Text format     Abstract available
    
    
    
35. TANTSIS EM, Gill D, Griffiths L, Gupta S, et al
    Eye movement disorders are an early manifestation of CACNA1A mutations in children.
    Dev Med Child Neurol. 2016;58:639-44.
    PubMed     Text format     Abstract available
    
    

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