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Articles published in Brain Dev

Retrieve available abstracts of 82 articles:
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Single Articles


    July 2019
  1. MIR A, Chaudhary M, Alkhaldi H, Alhazmi R, et al
    Corrigendum to "Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10" [Brain Dev 2019].
    Brain Dev. 2019 Jul 19. pii: S0387-7604(19)30324.
    PubMed     Text format    


  2. KWONG AK, Chu VL, Rodenburg RJT, Smeitink J, et al
    ARX-associated infantile epileptic-dyskinetic encephalopathy with responsiveness to valproate for controlling seizures and reduced activity of muscle mitochondrial complex IV.
    Brain Dev. 2019 Jul 16. pii: S0387-7604(19)30180.
    PubMed     Text format     Abstract available


    June 2019
  3. KAMATE M, Detroja M, Hattiholi V
    Neuronal ceroid lipofuscinosis type-11 in an adolescent.
    Brain Dev. 2019;41:542-545.
    PubMed     Text format     Abstract available


  4. LENCI G, Calevo MG, Gaggero R, Prato G, et al
    Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome.
    Brain Dev. 2019;41:522-530.
    PubMed     Text format     Abstract available


  5. ENOKIZONO M, Sato N, Ota M, Shigemoto Y, et al
    Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly.
    Brain Dev. 2019;41:507-515.
    PubMed     Text format     Abstract available


    May 2019
  6. MATSUURA R, Hamano SI, Kubota J, Daida A, et al
    Efficacy and safety of pyridoxal in West syndrome: A retrospective study.
    Brain Dev. 2019;41:413-419.
    PubMed     Text format     Abstract available


    April 2019
  7. BEKTAS G, Kipoglu O, Pembegul Yildiz E, Aydinli N, et al
    Epileptic spasm and other forms of epilepsy in presumed perinatal arterial ischemic stroke in Turkey after more than 10years follow-up: A single centre study.
    Brain Dev. 2019 Apr 16. pii: S0387-7604(19)30095.
    PubMed     Text format     Abstract available


  8. MIR A, Chaudhary M, Alkhaldi H, Alhazmi R, et al
    Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10.
    Brain Dev. 2019 Apr 2. pii: S0387-7604(18)30126.
    PubMed     Text format     Abstract available


  9. TURKDOGAN D, Thomas G, Demirel B
    Ketogenic diet as a successful early treatment modality for SCN2A mutation.
    Brain Dev. 2019;41:389-391.
    PubMed     Text format     Abstract available


  10. OKUZONO S, Fukai R, Noda M, Miyake N, et al
    An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome.
    Brain Dev. 2019;41:378-381.
    PubMed     Text format     Abstract available


    February 2019
  11. OKUMURA A, Kurahashi H, Iwayama H, Numoto S, et al
    Serum carnitine levels of children with epilepsy: Related factors including valproate.
    Brain Dev. 2019 Feb 28. pii: S0387-7604(18)30643.
    PubMed     Text format     Abstract available


  12. BROZOVA K, Broz J
    The risk of hypoglycemia and the ketogenic diet for super-refractory status epilepticus patients.
    Brain Dev. 2019 Feb 22. pii: S0387-7604(19)30090.
    PubMed     Text format    


    January 2019
  13. LOTTI F, Geronzi U, Grosso S
    Electroencephalographic and epilepsy findings in mecp2 duplication syndrome. A family study.
    Brain Dev. 2019 Jan 11. pii: S0387-7604(18)30193.
    PubMed     Text format     Abstract available


  14. PARK EG, Lee J, Lee J
    The ketogenic diet for super-refractory status epilepticus patients in intensive care units.
    Brain Dev. 2019 Jan 9. pii: S0387-7604(18)30173.
    PubMed     Text format     Abstract available


  15. ARAI Y, Iwasaki Y, Suzuki T, Ide S, et al
    Elimination of amyloid precursor protein in senile plaques in the brain of a patient with Alzheimer-type dementia and Down syndrome.
    Brain Dev. 2019;41:106-110.
    PubMed     Text format     Abstract available


    December 2018
  16. ARAYAKARNKUL P, Chomtho K
    Treatment options in pediatric super-refractory status epilepticus.
    Brain Dev. 2018 Dec 7. pii: S0387-7604(18)30088.
    PubMed     Text format     Abstract available


    November 2018
  17. 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


  18. KIM SH, Kang HC, Lee JS, Kim HD, et al
    Rufinamide efficacy and safety in children aged 1-4years with Lennox-Gastaut syndrome.
    Brain Dev. 2018;40:897-903.
    PubMed     Text format     Abstract available


  19. TAKEZAWA Y, Fujie H, Kikuchi A, Niihori T, et al
    Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome.
    Brain Dev. 2018;40:934-938.
    PubMed     Text format     Abstract available


  20. ISOBE K, Matsumoto H, Tamura Y, Hashimoto J, et al
    Infantile spasms in a mosaic monocentric and duplicated SMC 15 patient.
    Brain Dev. 2018;40:891-896.
    PubMed     Text format     Abstract available


  21. TAKANASHI JI, Yasukawa K, Murofushi Y, Masunaga A, et al
    Loss of myelinated axons and astrocytosis in an autopsy case of acute encephalopathy with biphasic seizures and late reduced diffusion.
    Brain Dev. 2018;40:947-951.
    PubMed     Text format     Abstract available


    October 2018
  22. 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


  23. 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


  24. 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
  25. 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


  26. 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


  27. 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
  28. 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


  29. 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
  30. 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


  31. 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
  32. 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


  33. 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


  34. 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


  35. 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
  36. 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


  37. 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


  38. 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


  39. 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


  40. 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
  41. 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


  42. 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


  43. 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
  44. 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


  45. 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
  46. 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


  47. 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
  48. 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


  49. 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    


  50. 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


  51. 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


  52. 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


  53. 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


  54. 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
  55. 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


  56. 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


  57. 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
  58. 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


  59. 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
  60. 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


  61. 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


  62. 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
  63. 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


  64. 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


  65. 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
  66. 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
  67. 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


  68. 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


  69. 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


  70. 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


  71. 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
  72. 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


  73. 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


  74. 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


  75. 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
  76. 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


  77. 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


  78. 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


  79. 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


  80. 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
  81. 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


  82. 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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