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Articles published in Brain Dev

Retrieve available abstracts of 62 articles:
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Single Articles


    November 2018
  1. ISHIHARA N, Inagaki H, Miyake M, Kawamura Y, et al
    A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant.
    Brain Dev. 2018 Nov 1. pii: S0387-7604(18)30256.
    PubMed     Text format     Abstract available


    October 2018
  2. MAGARA S, Komatsubara T, Hojo M, Kobayashi Y, et al
    The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children.
    Brain Dev. 2018 Oct 17. pii: S0387-7604(18)30468.
    PubMed     Text format     Abstract available


  3. KANAI S, Okanishi T, Fujimoto A, Itamura S, et al
    Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome.
    Brain Dev. 2018 Oct 9. pii: S0387-7604(18)30252.
    PubMed     Text format     Abstract available


  4. YASUMOTO S, Ohtsuka Y, Sato K, Kurata A, et al
    Long-term efficacy and safety of lamotrigine monotherapy in Japanese and South Korean pediatric patients with newly diagnosed typical absence seizures: An open-label extension study.
    Brain Dev. 2018;40:786-791.
    PubMed     Text format     Abstract available


    September 2018
  5. LEE EH, You SJ
    Factors associated with electroencephalographic and clinical remission of benign childhood epilepsy with centrotemporal spikes.
    Brain Dev. 2018 Sep 8. pii: S0387-7604(18)30372.
    PubMed     Text format     Abstract available


  6. HAMANO SI, Nagai T, Matsuura R, Hirata Y, et al
    Treatment of infantile spasms by pediatric neurologists in Japan.
    Brain Dev. 2018;40:685-692.
    PubMed     Text format     Abstract available


  7. SU DJ, Lu JF, Lin LJ, Liang JS, et al
    SCN2A mutation in an infant presenting with migrating focal seizures and infantile spasm responsive to a ketogenic diet.
    Brain Dev. 2018;40:724-727.
    PubMed     Text format     Abstract available


    August 2018
  8. NISHIYAMA M, Nagase H, Tomioka K, Tanaka T, et al
    Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticus.
    Brain Dev. 2018 Aug 22. pii: S0387-7604(18)30391.
    PubMed     Text format     Abstract available


  9. AMANO Y, Fujimoto A, Okanishi T, Nishimura M, et al
    Dense array EEG estimated the epileptic focus in a patient with epilepsy secondary to tuberous sclerosis complex.
    Brain Dev. 2018 Aug 1. pii: S0387-7604(18)30186.
    PubMed     Text format     Abstract available


    July 2018
  10. KIMURA N, Takahashi Y, Shigematsu H, Imai K, et al
    Risk factors of cognitive impairment in pediatric epilepsy patients with focal cortical dysplasia.
    Brain Dev. 2018 Jul 31. pii: S0387-7604(18)30345.
    PubMed     Text format     Abstract available


  11. MIZUGUCHI M, Ikeda H, Kagitani-Shimono K, Yoshinaga H, et al
    Everolimus for epilepsy and autism spectrum disorder in tuberous sclerosis complex: EXIST-3 substudy in Japan.
    Brain Dev. 2018 Jul 27. pii: S0387-7604(18)30176.
    PubMed     Text format     Abstract available


    June 2018
  12. TEKTURK P, Baykan B, Erdag E, Peach S, et al
    Investigation of neuronal auto-antibodies in children diagnosed with epileptic encephalopathy of unknown cause.
    Brain Dev. 2018 Jun 20. pii: S0387-7604(18)30254.
    PubMed     Text format     Abstract available


  13. OKAMOTO K, Fukuda M, Saito I, Horiuchi I, et al
    Incidence of childhood epilepsy: A population-based study in rural Japan.
    Brain Dev. 2018 Jun 19. pii: S0387-7604(18)30258.
    PubMed     Text format     Abstract available


  14. ALHAKEEM A, Alshibani F, Tabarki B
    Extending the use of stiripentol to SLC13A5-related epileptic encephalopathy.
    Brain Dev. 2018 Jun 9. pii: S0387-7604(18)30245.
    PubMed     Text format     Abstract available


  15. YANAGISHITA T, Ito S, Ohtani Y, Eto K, et al
    Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG.
    Brain Dev. 2018 Jun 6. pii: S0387-7604(18)30232.
    PubMed     Text format     Abstract available


    May 2018
  16. MARZIN P, Mignot C, Dorison N, Dufour L, et al
    Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.
    Brain Dev. 2018 May 31. pii: S0387-7604(18)30214.
    PubMed     Text format     Abstract available


  17. SHIMADA S, Oguni H, Otani Y, Nishikawa A, et al
    An episode of acute encephalopathy with biphasic seizures and late reduced diffusion followed by hemiplegia and intractable epilepsy observed in a patient with a novel frameshift mutation in HNRNPU.
    Brain Dev. 2018 May 29. pii: S0387-7604(18)30220.
    PubMed     Text format     Abstract available


  18. CHIANG LM, Huang GS, Sun CC, Hsiao YL, et al
    Association of developing childhood epilepsy subsequent to febrile seizure: A population-based cohort study.
    Brain Dev. 2018 May 22. pii: S0387-7604(18)30211.
    PubMed     Text format     Abstract available


  19. KIM H, Kim SY, Lim BC, Hwang H, et al
    Spike persistence and normalization in benign epilepsy with centrotemporal spikes - Implications for management.
    Brain Dev. 2018 May 10. pii: S0387-7604(18)30184.
    PubMed     Text format     Abstract available


  20. KOBAYASHI K, Ohuchi Y, Shibata T, Hanaoka Y, et al
    Detection of fast (40-150Hz) oscillations from the ictal scalp EEG data of myoclonic seizures in pediatric patients.
    Brain Dev. 2018;40:397-405.
    PubMed     Text format     Abstract available


    April 2018
  21. TAKEGUCHI R, Haginoya K, Uchiyama Y, Fujita A, et al
    Two Japanese cases of epileptic encephalopathy associated with an FGF12 mutation.
    Brain Dev. 2018 Apr 23. pii: S0387-7604(18)30135.
    PubMed     Text format     Abstract available


  22. HAUSMAN-KEDEM M, Menascu S, Kramer U
    Efficacy of CBD-enriched medical cannabis for treatment of refractory epilepsy in children and adolescents - An observational, longitudinal study.
    Brain Dev. 2018 Apr 16. pii: S0387-7604(18)30112.
    PubMed     Text format     Abstract available


  23. KIM HW, Quan Z, Kim YB, Cheong E, et al
    Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients.
    Brain Dev. 2018;40:287-298.
    PubMed     Text format     Abstract available


    March 2018
  24. TAKAYAMA R, Imai K, Ikeda H, Baba K, et al
    Successful hemispherotomy in two refractory epilepsy patients with cerebral hemiatrophy and contralateral EEG abnormalities.
    Brain Dev. 2018 Mar 14. pii: S0387-7604(18)30060.
    PubMed     Text format     Abstract available


  25. XIE LL, Song XJ, Li TY, Jiang L, et al
    A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twins.
    Brain Dev. 2018 Mar 1. pii: S0387-7604(18)30041.
    PubMed     Text format     Abstract available


    February 2018
  26. MYERS KA, Scheffer IE, Archer JS
    Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotype.
    Brain Dev. 2018 Feb 16. pii: S0387-7604(18)30010.
    PubMed     Text format     Abstract available


  27. KIM H, Lee S, Choi M, Kim H, et al
    Familial cases of progressive myoclonic epilepsy caused by maternal somatic mosaicism of a recurrent KCNC1 p.Arg320His mutation.
    Brain Dev. 2018 Feb 8. pii: S0387-7604(18)30011.
    PubMed     Text format     Abstract available


    January 2018
  28. SCHIRINZI T, Graziola F, Cusmai R, Fusco L, et al
    ATP1A3-related epileptic encephalopathy responding to ketogenic diet.
    Brain Dev. 2018 Jan 26. pii: S0387-7604(18)30006.
    PubMed     Text format     Abstract available


  29. LATTANZI S, Cagnetti C, Matricardi S, Silvestrini M, et al
    Palliative non-resective surgery for drug-resistant epilepsy.
    Brain Dev. 2018 Jan 13. pii: S0387-7604(17)30355.
    PubMed     Text format    


  30. GONG P, Xue J, Qian P, Yang H, et al
    Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies.
    Brain Dev. 2018 Jan 4. pii: S0387-7604(17)30353.
    PubMed     Text format     Abstract available


  31. GULATI S, Sondhi V, Chakrabarty B, Jauhari P, et al
    High dose phenobarbitone coma in pediatric refractory status epilepticus; a retrospective case record analysis, a proposed protocol and review of literature.
    Brain Dev. 2018 Jan 3. pii: S0387-7604(17)30304.
    PubMed     Text format     Abstract available


  32. NARDELLO R, Fontana A, Antona V, Beninati A, et al
    A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability.
    Brain Dev. 2018;40:58-64.
    PubMed     Text format     Abstract available


  33. SPAGNOLI C, Salerno GG, Iodice A, Frattini D, et al
    KCNQ2 encephalopathy: A case due to a de novo deletion.
    Brain Dev. 2018;40:65-68.
    PubMed     Text format     Abstract available


  34. KOJIMA K, Shirai K, Kobayashi M, Miyauchi A, et al
    A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation.
    Brain Dev. 2018;40:69-73.
    PubMed     Text format     Abstract available


    December 2017
  35. NAVARRO-ABIA V, Soriano-Ramos M, Nunez-Enamorado N, Camacho-Salas A, et al
    Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review.
    Brain Dev. 2017 Dec 30. pii: S0387-7604(17)30311.
    PubMed     Text format     Abstract available


  36. ALSHAHAWY AK, Darwish AH, Elsaid Shalaby S, Mawlana W, et al
    Prevalence of idiopathic epilepsy among school children in Gharbia Governorate, Egypt.
    Brain Dev. 2017 Dec 30. pii: S0387-7604(17)30352.
    PubMed     Text format     Abstract available


  37. JESMANAS S, Norvainyte K, Gleizniene R, Simoliuniene R, et al
    Different MRI-defined tuber types in tuberous sclerosis complex: Quantitative evaluation and association with disease manifestations.
    Brain Dev. 2017 Dec 16. pii: S0387-7604(17)30305.
    PubMed     Text format     Abstract available


    November 2017
  38. OKANISHI T, Fujimoto A, Hashimoto R, Nishimura M, et al
    Epileptic spasms secondary to acute cerebral and cerebellar encephalitis.
    Brain Dev. 2017 Nov 29. pii: S0387-7604(17)30278.
    PubMed     Text format     Abstract available


  39. KUMADA T, Imai K, Takahashi Y, Nabatame S, et al
    Ketogenic diet using a Japanese ketogenic milk for patients with epilepsy: A multi-institutional study.
    Brain Dev. 2017 Nov 25. pii: S0387-7604(17)30275.
    PubMed     Text format     Abstract available


    October 2017
  40. YANG X, Qian P, Xu X, Liu X, et al
    GRIN2A mutations in epilepsy-aphasia spectrum disorders.
    Brain Dev. 2017 Oct 19. pii: S0387-7604(17)30261.
    PubMed     Text format     Abstract available


  41. MADAAN P, Jauhari P, Gupta A, Chakrabarty B, et al
    A quinidine non responsive novel KCNT1 mutation in an Indian infant with epilepsy of infancy with migrating focal seizures.
    Brain Dev. 2017 Oct 13. pii: S0387-7604(17)30262.
    PubMed     Text format     Abstract available


  42. LEE HJ, Kim EH, Yum MS, Ko TS, et al
    Attention profiles in childhood absence epilepsy compared with attention-deficit/hyperactivity disorder.
    Brain Dev. 2017 Oct 6. pii: S0387-7604(17)30260.
    PubMed     Text format     Abstract available


    September 2017
  43. ZHANG H, Zhang W, Li Y, Yan J, et al
    Correlations between UGT2B7 *2 gene polymorphisms and plasma concentrations of carbamazepine and valproic acid in epilepsy patients.
    Brain Dev. 2017 Sep 25. pii: S0387-7604(17)30241.
    PubMed     Text format     Abstract available


  44. HAYASHIDA T, Saito Y, Ishii A, Yamada H, et al
    CACNA1A-related early-onset encephalopathy with myoclonic epilepsy: A case report.
    Brain Dev. 2017 Sep 16. pii: S0387-7604(17)30237.
    PubMed     Text format     Abstract available


  45. NAKAMURA Y, Togawa Y, Okuno Y, Muramatsu H, et al
    Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum.
    Brain Dev. 2017 Sep 8. pii: S0387-7604(17)30234.
    PubMed     Text format     Abstract available


    August 2017
  46. IKEDA H, Imai K, Ikeda H, Matsuda K, et al
    Ictal single photon emission computed tomography of myoclonic absence seizures.
    Brain Dev. 2017 Aug 16. pii: S0387-7604(17)30210.
    PubMed     Text format     Abstract available


    July 2017
  47. OUYANG CS, Chiang CT, Yang RC, Wu RC, et al
    Quantitative EEG findings and response to treatment with antiepileptic medications in children with epilepsy.
    Brain Dev. 2017 Jul 27. pii: S0387-7604(17)30187.
    PubMed     Text format     Abstract available


  48. FUNATA K, Shike T, Takenouchi T, Yamashita Y, et al
    Respiratory arrest at the onset of idiopathic childhood occipital epilepsy of Gastaut.
    Brain Dev. 2017 Jul 19. pii: S0387-7604(17)30181.
    PubMed     Text format     Abstract available


  49. KOHASHI K, Ishiyama A, Yuasa S, Tanaka T, et al
    Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations.
    Brain Dev. 2017 Jul 17. pii: S0387-7604(17)30174.
    PubMed     Text format     Abstract available


  50. YANG Z, Li H, Xue J, Qian P, et al
    Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese children.
    Brain Dev. 2017 Jul 13. pii: S0387-7604(17)30179.
    PubMed     Text format     Abstract available


  51. LIANG JS, Lin LJ, Yang MT, Wang JS, et al
    The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features.
    Brain Dev. 2017 Jul 11. pii: S0387-7604(17)30172.
    PubMed     Text format     Abstract available


    May 2017
  52. BONANNI P, Negrin S, Volzone A, Zanotta N, et al
    Electrical status epilepticus during sleep in Mowat-Wilson syndrome.
    Brain Dev. 2017 May 10. pii: S0387-7604(17)30119.
    PubMed     Text format     Abstract available


  53. TAKEDA K, Matsuda H, Miyamoto Y, Yamamoto H, et al
    Structural brain network analysis of children with localization-related epilepsy.
    Brain Dev. 2017 May 6. pii: S0387-7604(17)30116.
    PubMed     Text format     Abstract available


  54. ISIK U, Dincer A
    Central tegmentum tract hyperintensities in pediatric neurological patients: Incidence or coincidence.
    Brain Dev. 2017;39:411-417.
    PubMed     Text format     Abstract available


  55. NUMOTO S, Kurahashi H, Azuma Y, Numaguchi A, et al
    Fournier's gangrene during ACTH therapy.
    Brain Dev. 2017;39:435-438.
    PubMed     Text format     Abstract available


    April 2017
  56. LIN JJ, Chou CC, Lan SY, Hsiao HJ, et al
    Therapeutic burst-suppression coma in pediatric febrile refractory status epilepticus.
    Brain Dev. 2017 Apr 19. pii: S0387-7604(17)30110.
    PubMed     Text format     Abstract available


  57. KIM SH, Kang HC, Lee EJ, Lee JS, et al
    Low glycemic index treatment in patients with drug-resistant epilepsy.
    Brain Dev. 2017 Apr 18. pii: S0387-7604(17)30104.
    PubMed     Text format     Abstract available


  58. KURAHASHI N, Miyake N, Mizuno S, Koshimizu E, et al
    Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations.
    Brain Dev. 2017 Apr 9. pii: S0387-7604(17)30085.
    PubMed     Text format     Abstract available


  59. GROSSO S, Ferranti S, Gaggiano C, Grande E, et al
    Massive lamotrigine poisoning. A case report.
    Brain Dev. 2017;39:349-351.
    PubMed     Text format     Abstract available


  60. MASRI A, Chung SK, Rees MI
    Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patients.
    Brain Dev. 2017;39:306-311.
    PubMed     Text format     Abstract available


    March 2017
  61. KIZTANIR H, Bektas G, Yildiz EP, Uzunhan TA, et al
    Coexisting neuronal autoantibodies among children with demyelinating syndromes.
    Brain Dev. 2017;39:248-251.
    PubMed     Text format     Abstract available


  62. KOBAYASHI Y, Tohyama J, Akiyama T, Magara S, et al
    Severe leukoencephalopathy with cortical involvement and peripheral neuropathy due to FOLR1 deficiency.
    Brain Dev. 2017;39:266-270.
    PubMed     Text format     Abstract available


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