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Articles published in Dev Med Child Neurol

Retrieve available abstracts of 33 articles:
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Single Articles


    November 2017
  1. 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.
    PubMed     Text format    


  2. 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
  3. 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


  4. 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
  5. 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
  6. 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
  7. 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


  8. 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
  9. RUBBOLI G
    Perampanel in refractory epilepsies: what real-life experience tells us.
    Dev Med Child Neurol. 2017 Jan 27. doi: 10.1111/dmcn.13384.
    PubMed     Text format    


  10. DAN B
    Gap junctions in epilepsy: for better or worse.
    Dev Med Child Neurol. 2017;59:4.
    PubMed     Text format    


    December 2016
  11. HEYMAN E, Lahat E, Levin N, Epstein O, et al
    Tolerability and efficacy of perampanel in children with refractory epilepsy.
    Dev Med Child Neurol. 2016 Dec 9. doi: 10.1111/dmcn.13362.
    PubMed     Text format     Abstract available


    October 2016
  12. HIDALGO ET, Weiner HL
    Surgery for epileptogenic cerebral dysplasia in children.
    Dev Med Child Neurol. 2016 Oct 11. doi: 10.1111/dmcn.13292.
    PubMed     Text format     Abstract available


    September 2016
  13. SANCHEZ FERNANDEZ I, Loddenkemper T
    Interictal epileptiform discharges and cognition.
    Dev Med Child Neurol. 2016 Sep 2. doi: 10.1111/dmcn.13245.
    PubMed     Text format    


    August 2016
  14. GROPPEL G, Dorfer C, Dressler A, Muhlebner A, et al
    Immediate termination of electrical status epilepticus in sleep after hemispherotomy is associated with significant progress in language development.
    Dev Med Child Neurol. 2016 Aug 25. doi: 10.1111/dmcn.13233.
    PubMed     Text format     Abstract available


  15. RIVKIN MJ
    Epilepsy as the 'echo' of acute stroke in children.
    Dev Med Child Neurol. 2016 Aug 13. doi: 10.1111/dmcn.13231.
    PubMed     Text format    


    July 2016
  16. FOX CK, Mackay MT, Dowling MM, Pergami P, et al
    Prolonged or recurrent acute seizures after pediatric arterial ischemic stroke are associated with increasing epilepsy risk.
    Dev Med Child Neurol. 2016 Jul 16. doi: 10.1111/dmcn.13198.
    PubMed     Text format     Abstract available


    June 2016
  17. URQUHART DS, Kehinde OO, Mclellan AE
    Observational pilot study of reported symptoms of obstructive sleep apnoea in children with epilepsy.
    Dev Med Child Neurol. 2016 Jun 18. doi: 10.1111/dmcn.13173.
    PubMed     Text format     Abstract available


  18. VARADKAR S
    The biochemical basis of genetic epilepsies and the genetic basis of inherited metabolic disease.
    Dev Med Child Neurol. 2016 Jun 15. doi: 10.1111/dmcn.13184.
    PubMed     Text format    


  19. 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


  20. 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


  21. 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


    May 2016
  22. BARBA C, Darra F, Cusmai R, Procopio E, et al
    Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy.
    Dev Med Child Neurol. 2016 May 13. doi: 10.1111/dmcn.13141.
    PubMed     Text format     Abstract available


    April 2016
  23. MOHAMMAD SS, Jones H, Hong M, Nosadini M, et al
    Symptomatic treatment of children with anti-NMDAR encephalitis.
    Dev Med Child Neurol. 2016;58:376-84.
    PubMed     Text format     Abstract available


    March 2016
  24. GARCIA J, Wical B, Wical W, Schaffer L, et al
    Obstructive sleep apnea in children with cerebral palsy and epilepsy.
    Dev Med Child Neurol. 2016 Mar 16. doi: 10.1111/dmcn.13091.
    PubMed     Text format     Abstract available


    February 2016
  25. PEARL PL
    From gene discovery to precision intervention in epilepsy: almost the end of the beginning.
    Dev Med Child Neurol. 2016 Feb 18. doi: 10.1111/dmcn.13078.
    PubMed     Text format    


  26. DELACY MJ, Reid SM
    Profile of associated impairments at age 5 years in Australia by cerebral palsy subtype and Gross Motor Function Classification System level for birth years 1996 to 2005.
    Dev Med Child Neurol. 2016;58 Suppl 2:50-6.
    PubMed     Text format     Abstract available


  27. REID SM, Meehan E, McIntyre S, Goldsmith S, et al
    Temporal trends in cerebral palsy by impairment severity and birth gestation.
    Dev Med Child Neurol. 2016;58 Suppl 2:25-35.
    PubMed     Text format     Abstract available


    January 2016
  28. KIRTON A
    Filling a lacune in perinatal stroke outcomes.
    Dev Med Child Neurol. 2016;58:8-9.
    PubMed     Text format    


  29. ECURY-GOOSSEN GM, van der Haer M, Smit LS, Feijen-Roon M, et al
    Neurodevelopmental outcome after neonatal perforator stroke.
    Dev Med Child Neurol. 2016;58:49-56.
    PubMed     Text format     Abstract available


    December 2015
  30. PAPANDREOU A, McTague A, Trump N, Ambegaonkar G, et al
    GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy.
    Dev Med Child Neurol. 2015 Dec 9. doi: 10.1111/dmcn.12976.
    PubMed     Text format     Abstract available


    November 2015
  31. TOKER O, Tal Y, Horev L, Shmoeli D, et al
    Valproic acid hypersensitivity and desensitization.
    Dev Med Child Neurol. 2015;57:1076-8.
    PubMed     Text format     Abstract available


    October 2015
  32. KLEPPER J
    GLUT1 deficiency syndrome and ketogenic diet therapies: missing rare but treatable diseases?
    Dev Med Child Neurol. 2015;57:896-7.
    PubMed     Text format    


  33. SCHOELER NE, Cross JH, Drury S, Lench N, et al
    Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factor.
    Dev Med Child Neurol. 2015;57:969-76.
    PubMed     Text format     Abstract available


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