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Articles published in Brain Dev

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Single Articles


    August 2018
  1. 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
  2. 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


  3. 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
  4. 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


  5. 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


  6. 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


  7. 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
  8. 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


  9. 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


  10. 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


  11. 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


    April 2018
  12. 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


  13. 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


    March 2018
  14. 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


  15. 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
  16. 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


  17. 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
  18. 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


  19. 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    


  20. 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


  21. 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


  22. 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


  23. 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


  24. 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
  25. 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


  26. 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


  27. 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
  28. 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


  29. 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
  30. 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


  31. 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


  32. 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
  33. 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


  34. 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


  35. 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
  36. 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
  37. 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


  38. 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


  39. 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


  40. 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


  41. 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
  42. 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


  43. 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


  44. 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


  45. 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
  46. 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


  47. 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


  48. 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


  49. 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


  50. 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
  51. 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


  52. 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


    February 2017
  53. PANTELIADIS CP, Vassilyadi P, Fehlert J, Hagel C, et al
    Historical documents on epilepsy: From antiquity through the 20th century.
    Brain Dev. 2017 Feb 26. pii: S0387-7604(17)30029.
    PubMed     Text format     Abstract available


  54. LI H, Xue J, Qian P, Zhang Y, et al
    Electro-clinical-etiological associations of epilepsia partialis continua in 57 Chinese children.
    Brain Dev. 2017 Feb 18. pii: S0387-7604(17)30011.
    PubMed     Text format     Abstract available


  55. BEKTAS G, Tekin U, Yildiz EP, Uzunhan TA, et al
    Psychosocial and behavioral functioning and their relationship to seizure timing in children with benign epilepsy with centrotemporal spikes.
    Brain Dev. 2017 Feb 14. pii: S0387-7604(17)30013.
    PubMed     Text format     Abstract available


  56. MOAVERO R, Santarone ME, Galasso C, Curatolo P, et al
    Cognitive and behavioral effects of new antiepileptic drugs in pediatric epilepsy.
    Brain Dev. 2017 Feb 12. pii: S0387-7604(17)30006.
    PubMed     Text format     Abstract available


  57. LEE D, Liang J, Hur YJ, Kim NY, et al
    Spectral characteristics of intracranial electroencephalographic activity in patients with Lennox-Gastaut syndrome.
    Brain Dev. 2017;39:138-144.
    PubMed     Text format     Abstract available


  58. MATSUO M, Yamauchi A, Ito Y, Sakauchi M, et al
    Mandibulofacial dysostosis with microcephaly: A case presenting with seizures.
    Brain Dev. 2017;39:177-181.
    PubMed     Text format     Abstract available


  59. ALTUNEL A, Sever A, Altunel EO
    ACTH has beneficial effects on stuttering in ADHD and ASD patients with ESES: A retrospective study.
    Brain Dev. 2017;39:130-137.
    PubMed     Text format     Abstract available


    January 2017
  60. NATSUME J, Hamano SI, Iyoda K, Kanemura H, et al
    New guidelines for management of febrile seizures in Japan.
    Brain Dev. 2017;39:2-9.
    PubMed     Text format     Abstract available


  61. FUKUOKA M, Kuki I, Kawawaki H, Okazaki S, et al
    Quinidine therapy for West syndrome with KCNTI mutation: A case report.
    Brain Dev. 2017;39:80-83.
    PubMed     Text format     Abstract available


  62. TAKAORI T, Kumakura A, Ishii A, Hirose S, et al
    Two mild cases of Dravet syndrome with truncating mutation of SCN1A.
    Brain Dev. 2017;39:72-74.
    PubMed     Text format     Abstract available


  63. KOBAYASHI Y, Hanaoka Y, Akiayma T, Ohmori I, et al
    A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data.
    Brain Dev. 2017;39:75-79.
    PubMed     Text format     Abstract available


  64. KUYA K, Fujii S, Miyoshi F, Ohno K, et al
    A case of acute encephalopathy with biphasic seizures and late reduced diffusion: Utility of arterial spin labeling sequence.
    Brain Dev. 2017;39:84-88.
    PubMed     Text format     Abstract available


    December 2016
  65. OKANISHI T, Fujimoto A, Motoi H, Kanai S, et al
    Total corpus callosotomy for epileptic spasms after acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in a case with tuberous sclerosis complex.
    Brain Dev. 2016 Dec 3. pii: S0387-7604(16)30195.
    PubMed     Text format     Abstract available


  66. FIUMARA A, Barone R, Del Campo G, Striano P, et al
    Early-Onset Epileptic Encephalopathy in infants with different forms of Congenital Disorders of Glycosylation (CDG).
    Brain Dev. 2016 Dec 3. pii: S0387-7604(16)30193.
    PubMed     Text format    


  67. HINO-FUKUYO N, Kikuchi A, Iwasaki M, Sato Y, et al
    Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation.
    Brain Dev. 2016 Dec 1. pii: S0387-7604(16)30191.
    PubMed     Text format     Abstract available


    November 2016
  68. FINSTERER J, Zarrouk-Mahjoub S
    Epilepsia partialis continua in MELAS/Leigh overlap syndrome.
    Brain Dev. 2016 Nov 30. pii: S0387-7604(16)30189.
    PubMed     Text format    


  69. DILENA R, Striano P, Gennaro E, Bassi L, et al
    Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy.
    Brain Dev. 2016 Nov 19. pii: S0387-7604(16)30184.
    PubMed     Text format     Abstract available


  70. HANAOKA Y, Yoshinaga H, Kobayashi K
    A ten-year follow-up cohort study of childhood epilepsy: Changes in epilepsy diagnosis with age.
    Brain Dev. 2016 Nov 12. pii: S0387-7604(16)30180.
    PubMed     Text format     Abstract available


  71. BABA S, Sugawara Y, Moriyama K, Inaji M, et al
    Amelioration of intractable epilepsy by adjunct vagus nerve stimulation therapy in a girl with a CDKL5 mutation.
    Brain Dev. 2016 Nov 4. pii: S0387-7604(16)30176.
    PubMed     Text format     Abstract available


  72. MATSUDA T, Shimakawa S, Toshikawa H, Hatanaka M, et al
    Hippocampal signal abnormality on the first day of illness in acute encephalopathy with biphasic seizures and late reduced diffusion caused by HHV-6 infection.
    Brain Dev. 2016;38:943-946.
    PubMed     Text format     Abstract available


  73. MARUYAMA S, Okamoto Y, Toyoshima M, Hanaya R, et al
    Immunoglobulin A deficiency following treatment with lamotrigine.
    Brain Dev. 2016;38:947-949.
    PubMed     Text format     Abstract available


    October 2016
  74. MURAMATSU K, Sawaura N, Ogata T, Makioka N, et al
    Efficacy and tolerability of levetiracetam for pediatric refractory epilepsy.
    Brain Dev. 2016 Oct 13. pii: S0387-7604(16)30157.
    PubMed     Text format     Abstract available


  75. KIMIZU T, Takahashi Y, Oboshi T, Horino A, et al
    A case of early onset epileptic encephalopathy with de novo mutation in SLC35A2: Clinical features and treatment for epilepsy.
    Brain Dev. 2016 Oct 12. pii: S0387-7604(16)30158.
    PubMed     Text format     Abstract available


  76. KUGA S, Goto H, Okanari K, Maeda T, et al
    Reversible cerebral vasoconstriction syndrome manifesting as focal seizures without a thunderclap headache: A pediatric case report.
    Brain Dev. 2016;38:880-3.
    PubMed     Text format     Abstract available


  77. YOKOCHI T, Sakanishi S, Ishidou Y, Kawano G, et al
    Acute encephalopathy with biphasic seizures and late reduced diffusion associated with staphylococcal toxic shock syndrome caused by burns.
    Brain Dev. 2016;38:875-9.
    PubMed     Text format     Abstract available


  78. UEMATSU M, Haginoya K, Kikuchi A, Hino-Fukuyo N, et al
    Asymptomatic congenital cytomegalovirus infection with neurological sequelae: A retrospective study using umbilical cord.
    Brain Dev. 2016;38:819-26.
    PubMed     Text format     Abstract available


    September 2016
  79. GOWDA VK, Bhat MD, Srinivasan VM, Prasad C, et al
    A case of Canavan disease with microcephaly.
    Brain Dev. 2016;38:759-62.
    PubMed     Text format     Abstract available


  80. SATO Y, Numata-Uematsu Y, Uematsu M, Kikuchi A, et al
    Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus.
    Brain Dev. 2016;38:772-6.
    PubMed     Text format     Abstract available


    August 2016
  81. FUJII T, Ito Y, Takahashi S, Shimono K, et al
    Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey.
    Brain Dev. 2016;38:628-37.
    PubMed     Text format     Abstract available


  82. TAKAHASHI Y, Ueno K, Ninomiya Y, Eguchi T, et al
    Potential risk factors for dexmedetomidine withdrawal seizures in infants after surgery for congenital heart disease.
    Brain Dev. 2016;38:648-53.
    PubMed     Text format     Abstract available


  83. BEKTAS G, Caliskan M, Aydin A, Pembegul Yildiz E, et al
    Aggravation of atonic seizures by rufinamide: A case report.
    Brain Dev. 2016;38:654-7.
    PubMed     Text format     Abstract available


  84. BERNARDO P, Madia F, Santulli L, Del Gaudio L, et al
    17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.
    Brain Dev. 2016;38:663-8.
    PubMed     Text format     Abstract available


  85. ITAKURA A, Saito Y, Nishimura Y, Okazaki T, et al
    Successful treatment of migrating partial seizures in Wolf-Hirschhorn syndrome with bromide.
    Brain Dev. 2016;38:658-62.
    PubMed     Text format     Abstract available


    July 2016
  86. OKAZAKI T, Saito Y, Ueda R, Awashima T, et al
    Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis.
    Brain Dev. 2016 Jul 30. pii: S0387-7604(16)30100.
    PubMed     Text format     Abstract available


    June 2016
  87. KIM H, Yoo IH, Lim BC, Hwang H, et al
    Averaged EEG spike dipole analysis may predict atypical outcome in Benign Childhood Epilepsy with Centrotemporal Spikes (BCECTS).
    Brain Dev. 2016 Jun 18. pii: S0387-7604(16)30063.
    PubMed     Text format     Abstract available


  88. OLIVIERI G, Battaglia D, Chieffo D, Rubbino R, et al
    Cognitive-behavioral profiles in teenagers with Dravet syndrome.
    Brain Dev. 2016;38:554-62.
    PubMed     Text format     Abstract available


  89. MORI T, Imai K, Oboshi T, Fujiwara Y, et al
    Usefulness of ketogenic diet in a girl with migrating partial seizures in infancy.
    Brain Dev. 2016;38:601-4.
    PubMed     Text format     Abstract available


  90. KIM YO, Nam TS, Park C, Kim SK, et al
    Familial pachygyria in both genders related to a DCX mutation.
    Brain Dev. 2016;38:585-9.
    PubMed     Text format     Abstract available


    May 2016
  91. KOBAYASHI K, Akiyama T, Oka M, Endoh F, et al
    Fast (40-150Hz) oscillations are associated with positive slow waves in the ictal EEGs of epileptic spasms in West syndrome.
    Brain Dev. 2016 May 31. pii: S0387-7604(16)30060.
    PubMed     Text format     Abstract available


  92. INUI T, Kobayashi S, Ashikari Y, Sato R, et al
    Two cases of early-onset myoclonic seizures with continuous parietal delta activity caused by EEF1A2 mutations.
    Brain Dev. 2016;38:520-4.
    PubMed     Text format     Abstract available


  93. DUBEY R, Chakrabarty B, Saini L, Madaan P, et al
    Bilateral ophthalmoplegia in a child with migraine.
    Brain Dev. 2016;38:525-8.
    PubMed     Text format     Abstract available


    April 2016
  94. JOSHI C, Kolbe DL, Mansilla MA, Mason S, et al
    Ketogenic diet - A novel treatment for early epileptic encephalopathy due to PIGA deficiency.
    Brain Dev. 2016 Apr 25. pii: S0387-7604(16)30034.
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  95. HORINO A, Kawawaki H, Fukuoka M, Tsuji H, et al
    A case of succinic semialdehyde dehydrogenase deficiency with status epilepticus and rapid regression.
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  96. NASRI A, Bedoui I, Mrissa R, Riahi A, et al
    Recurrent status epilepticus in posterior reversible encephalopathy syndrome as initial feature of pediatric lupus: A newly diagnosed case and literature review.
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  97. OZDEMIR R, Kucuk M, Guzel O, Karadeniz C, et al
    Does ketogenic diet have any negative effect on cardiac systolic and diastolic functions in children with intractable epilepsy?: One-year follow-up results.
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  98. YASUMOTO S, Shimizu M, Sato K, Kurata A, et al
    Lamotrigine monotherapy for newly diagnosed typical absence seizures in children: A multi-center, uncontrolled, open-label study.
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  99. OKUMURA A, Nakahara E, Ikeno M, Abe S, et al
    Efficacy and tolerability of high-dose phenobarbital in children with focal seizures.
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  100. NAKATA M, Kato T, Ide M, Saito K, et al
    Long-term weekly ACTH therapy for relapsed West syndrome in tuberous sclerosis complex: A case report.
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    March 2016
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    The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy.
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  102. EKINCI O, Isik U, Gunes S, Yildirim C, et al
    Self-concept in children and adolescents with epilepsy: The role of family functioning, mothers' emotional symptoms and ADHD.
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  103. HIRANO Y, Oguni H, Nagata S
    Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome.
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  104. KATATA Y, Uematsu M, Sato H, Suzuki S, et al
    Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan.
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  105. ONO Y, Saito Y, Maegaki Y, Tohyama J, et al
    Three cases of right frontal megalencephaly: Clinical characteristics and long-term outcome.
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  106. MURATA S, Kashiwagi M, Tanabe T, Oba C, et al
    Targeted temperature management for acute encephalopathy in a Japanese secondary emergency medical care hospital.
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    February 2016
  107. KIM YO, Yang JH, Park C, Kim SK, et al
    A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy.
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  108. IGARASHI A, Okumura A, Shimojima K, Abe S, et al
    Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation.
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  109. KOBAYASHI S, Endo W, Inui T, Wakusawa K, et al
    The lack of antiepileptic drugs and worsening of seizures among physically handicapped patients with epilepsy during the Great East Japan Earthquake.
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    January 2016
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    Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes.
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  111. VEERAVIGROM M, Jaroonvanichkul V, Netbaramee W, Phaisarn P, et al
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  112. IWASAKI M, Uematsu M, Hino-Fukuyo N, Osawa S, et al
    Clinical profiles for seizure remission and developmental gains after total corpus callosotomy.
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    December 2015
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    Surgical versus medical treatment for children with epileptic encephalopathy in infancy and early childhood: Results of an international multicenter cohort study in Far-East Asia (the FACE study).
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    August 2015
  114. WONG VC, Fung CW, Kwong AK
    SCN2A mutation in a Chinese boy with infantile spasm - response to Modified Atkins Diet.
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    June 2015
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    Electroencephalographic features of patients with SCN1A-positive Dravet syndrome.
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  116. SARNAT HB, Flores-Sarnat L
    Infantile tauopathies: Hemimegalencephaly; tuberous sclerosis complex; focal cortical dysplasia 2; ganglioglioma.
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    Incidence of benign convulsions with mild gastroenteritis after introduction of rotavirus vaccine.
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    May 2015
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    Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phase.
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    April 2015
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    Efficacy and safety of fosphenytoin for acute encephalopathy in children.
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    March 2015
  120. SUZUKI K, Hiramoto A, Okumura T
    A case report on reversible Pelger-Huet anomaly depending on serum free fraction of valproic acid.
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  121. HWANG G, Kang HS, Park SY, Han KH, et al
    Predictors of unprovoked seizure after febrile seizure: short-term outcomes.
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  122. NISHIYAMA M, Tanaka T, Fujita K, Maruyama A, et al
    Targeted temperature management of acute encephalopathy without AST elevation.
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  123. GLASER K, Girschick HJ, Schropp C, Speer CP, et al
    Psychomotor development following early treatment of severe infantile vitamin B12 deficiency and West syndrome--is everything fine? A case report and review of literature.
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  124. HEYMAN E, Lahat E, Gandelman-Marton R
    Seizure occurrence during pediatric short-term EEG.
    Brain Dev. 2015;37:307-10.
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  125. HATANAKA M, Kashiwagi M, Tanabe T, Nakahara H, et al
    Overlapping MERS and mild AESD caused by HHV-6 infection.
    Brain Dev. 2015;37:334-8.
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