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Articles published in Brain Dev

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    July 2021
  1. COHEN H, Kramer U, Hausman-Kedem M, Uliel-Siboni S, et al
    Dosage of cannabidiol-enriched cannabis in children and adults with epilepsy.
    Brain Dev. 2021 Jul 2. pii: S0387-7604(21)00124.
    PubMed    


    June 2021
  2. CHEN W, Qin J, Shen Y, Liang J, et al
    Next generation sequencing in children with unexplained epilepsy: A retrospective cohort study.
    Brain Dev. 2021 Jun 10. pii: S0387-7604(21)00103.
    PubMed     Abstract available


  3. MATSUMOTO A, Kojima K, Miya F, Miyauchi A, et al
    Two cases of DYNC1H1 mutations with intractable epilepsy.
    Brain Dev. 2021 Jun 3. pii: S0387-7604(21)00094.
    PubMed     Abstract available


    May 2021
  4. HIRATA K, Sugawara Y, Hoshino A, Takeda S, et al
    Nonconvulsive status epilepticus following rotavirus gastroenteritis in two pediatric patients.
    Brain Dev. 2021 May 29. pii: S0387-7604(21)00098.
    PubMed     Abstract available


  5. OKA M, Kobayashi K, Shibata T, Tsuchiya H, et al
    A study on the relationship between non-epileptic fast (40 - 200 Hz) oscillations in scalp EEG and development in children.
    Brain Dev. 2021 May 26. pii: S0387-7604(21)00091.
    PubMed     Abstract available


  6. TIAN Q, Li H, Shu L, Wang H, et al
    Effective treatments for FGF12-related early-onset epileptic encephalopathies patients.
    Brain Dev. 2021 May 18. pii: S0387-7604(21)00088.
    PubMed     Abstract available


    April 2021
  7. KASRADZE S, Lomidze G, Cross JH, Kvernadze D, et al
    A six-year longitudinal study of neurocognitive problems in children with epilepsy.
    Brain Dev. 2021 Apr 20. pii: S0387-7604(21)00064.
    PubMed     Abstract available


  8. OGUNI H, Ito S, Nishikawa A, Otani Y, et al
    Morphometric analysis of spike-wave complexes (SWCs) causing myoclonic seizures in children with idiopathic myoclonic epilepsies - A positive SWC component correlates with myoclonic intensity.
    Brain Dev. 2021 Apr 16. pii: S0387-7604(21)00058.
    PubMed     Abstract available


  9. NEGISHI Y, Aoki Y, Itomi K, Yasuda K, et al
    SCN8A-related developmental and epileptic encephalopathy with ictal asystole requiring cardiac pacemaker implantation.
    Brain Dev. 2021 Apr 4. pii: S0387-7604(21)00061.
    PubMed     Abstract available


    March 2021
  10. PIETRAFUSA N, La Neve A, de Palma L, Boero G, et al
    Juvenile myoclonic epilepsy: Long-term prognosis and risk factors.
    Brain Dev. 2021 Mar 26. pii: S0387-7604(21)00042.
    PubMed     Abstract available


  11. MORI M, Kumada T, Inoue K, Nozaki F, et al
    Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitis.
    Brain Dev. 2021 Mar 10. pii: S0387-7604(21)00026.
    PubMed     Abstract available


    February 2021
  12. PORAT REIN A, Kramer U, Hausman Kedem M, Fattal-Valevski A, et al
    Early risk factors for encephalopathic transformation in children with benign childhood epilepsy with centrotemporal spikes.
    Brain Dev. 2021 Feb 14. pii: S0387-7604(21)00024.
    PubMed    


  13. NISHIYAMA M, Ishida Y, Yamaguchi H, Tokumoto S, et al
    Prediction of AESD and neurological sequelae in febrile status epilepticus.
    Brain Dev. 2021 Feb 7. pii: S0387-7604(21)00016.
    PubMed     Abstract available


    January 2021
  14. ITO S, Nagumo K, Nishikawa A, Oguni H, et al
    Low-dose phenobarbital for epilepsy with myoclonic absences: A case report.
    Brain Dev. 2021 Jan 15. pii: S0387-7604(20)30353.
    PubMed     Abstract available


  15. KOBAYASHI Y, Tohyama J, Takahashi Y, Goto T, et al
    Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variants.
    Brain Dev. 2021 Jan 9. pii: S0387-7604(20)30330.
    PubMed     Abstract available


    December 2020
  16. KIMURA S, Shiraishi H, Egawa K, Uchida M, et al
    Reply to the letter: "Perampanel may be beneficial in leigh syndrome by its anti-oxidative but not anti-epileptic effect".
    Brain Dev. 2020 Dec 11. pii: S0387-7604(20)30286.
    PubMed    


    November 2020
  17. MACROHON B, Janette Resurreccion-De La Calzada J, Sanchez-Gan B
    Clinical experience on the use of perampanel in epilepsy among child neurologists in the Philippines.
    Brain Dev. 2020 Nov 30. pii: S0387-7604(20)30316.
    PubMed     Abstract available


  18. SAENGOW VE, Chiangjong W, Khongkhatithum C, Changtong C, et al
    Proteomic analysis reveals plasma haptoglobin, interferon-gamma, and interleukin-1beta as potential biomarkers of pediatric refractory epilepsy.
    Brain Dev. 2020 Nov 30. pii: S0387-7604(20)30310.
    PubMed     Abstract available


  19. ANZAI R, Tsuji M, Yamashita S, Wada Y, et al
    Congenital disorders of glycosylation type IIb with MOGS mutations cause early infantile epileptic encephalopathy, dysmorphic features, and hepatic dysfunction.
    Brain Dev. 2020 Nov 28. pii: S0387-7604(20)30290.
    PubMed     Abstract available


  20. MIZUNO T, Miyata R, Hojo A, Tamura Y, et al
    Clinical variations of epileptic syndrome associated with PACS2 variant.
    Brain Dev. 2020 Nov 23. pii: S0387-7604(20)30284.
    PubMed     Abstract available


  21. PANDA PK, Sharawat IK
    Early risk factors for encephalopathic transformation in children with benign childhood epilepsy with centrotemporal spikes.
    Brain Dev. 2020 Nov 16. pii: S0387-7604(20)30292.
    PubMed    


  22. ITTIWUT C, Poonmaksatit S, Boonsimma P, Desudchit T, et al
    Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability.
    Brain Dev. 2020 Nov 12. pii: S0387-7604(20)30294.
    PubMed     Abstract available


    October 2020
  23. HUANG C, Li X, Wu L, Wu G, et al
    The effect of different dietary structure on gastrointestinal dysfunction in children with cerebral palsy and epilepsy based on gut microbiota.
    Brain Dev. 2020 Oct 15. pii: S0387-7604(20)30276.
    PubMed     Abstract available


    September 2020
  24. NA JH, Shin S, Yang D, Kim B, et al
    Corrigendum to 'Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy' [Brain Dev. 42(6) (2020) 438-448].
    Brain Dev. 2020 Sep 29. pii: S0387-7604(20)30269.
    PubMed    


  25. PORAT REIN A, Kramer U, Hausman Kedem M, Fattal-Valevski A, et al
    Early prediction of encephalopathic transformation in children with benign epilepsy with centro-temporal spikes.
    Brain Dev. 2020 Sep 7. pii: S0387-7604(20)30242.
    PubMed     Abstract available


  26. FINSTERER J
    Perampanel may be beneficial in Leigh syndrome by its anti-oxidative but not anti-epileptic effect.
    Brain Dev. 2020 Sep 3. pii: S0387-7604(20)30222.
    PubMed    


  27. SAMANTA D
    Epilepsy in Angelman syndrome: A scoping review.
    Brain Dev. 2020 Sep 3. pii: S0387-7604(20)30240.
    PubMed     Abstract available


    August 2020
  28. UEDA R, Kaga Y, Kita Y, Tanaka M, et al
    Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy.
    Brain Dev. 2020 Aug 29. pii: S0387-7604(20)30218.
    PubMed     Abstract available


  29. WANG X, Chen B, Jin L, Zhang W, et al
    Eight years follow-up of a generalized epilepsy patient with eating-induced late-onset epileptic spasms and atypical absence with myoclonic jerks.
    Brain Dev. 2020 Aug 10. pii: S0387-7604(20)30201.
    PubMed     Abstract available


  30. INUZUKA LM, Macedo-Souza LI, Della-Ripa B, Monteiro FP, et al
    Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy.
    Brain Dev. 2020 Aug 6. pii: S0387-7604(20)30144.
    PubMed     Abstract available


  31. HENRIKSEN MW, Breck H, Sejersted Y, Diseth T, et al
    Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.
    Brain Dev. 2020;42:484-495.
    PubMed     Abstract available


  32. HOSHIDE M, Yasudo H, Inoue H, Matsushige T, et al
    Efficacy of hypothermia therapy in patients with acute encephalopathy with biphasic seizures and late reduced diffusion.
    Brain Dev. 2020;42:515-522.
    PubMed     Abstract available


    July 2020
  33. KIMURA S, Shiraishi H, Egawa K, Uchida M, et al
    Efficacy of perampanel for epileptic seizures and daily behavior in a patient with Leigh syndrome: A case report.
    Brain Dev. 2020 Jul 29. pii: S0387-7604(20)30192.
    PubMed     Abstract available


  34. KUWAYAMA R, Suzuki Y, Nishikawa M, Kimizu T, et al
    Epilepsy in patients with advanced Fukuyama congenital muscular dystrophy.
    Brain Dev. 2020 Jul 25. pii: S0387-7604(20)30182.
    PubMed     Abstract available


  35. FURUICHI Y, Sakakibara T, Nezu S, Saeki K, et al
    Analysis of factors related to low health-related quality of life in children with epilepsy using a self-assessed Japanese version of the KIDSCREEN-52.
    Brain Dev. 2020 Jul 24. pii: S0387-7604(20)30185.
    PubMed     Abstract available


  36. ULIEL-SIBONY S, Hausman-Kedem M, Fattal-Valevski A, Kramer U, et al
    Cannabidiol-enriched oil in children and adults with treatment-resistant epilepsy-does tolerance exist?
    Brain Dev. 2020 Jul 24. pii: S0387-7604(20)30183.
    PubMed     Abstract available


  37. ZHU J, Xu C, Zhang X, Qiao L, et al
    The changes in the topological properties of brain structural network based on diffusion tensor imaging in pediatric epilepsy patients with vagus nerve stimulators: A graph theoretical analysis.
    Brain Dev. 2020 Jul 23. pii: S0387-7604(20)30189.
    PubMed     Abstract available


  38. TOGASHI N, Fujita A, Shibuya M, Uneoka S, et al
    Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy.
    Brain Dev. 2020 Jul 9. pii: S0387-7604(20)30175.
    PubMed     Abstract available


  39. TSUCHIYA H, Endoh F, Akiyama T, Matsuhashi M, et al
    Longitudinal correspondence of epilepsy and scalp EEG fast (40-200 Hz) oscillations in pediatric patients with tuberous sclerosis complex.
    Brain Dev. 2020 Jul 4. pii: S0387-7604(20)30152.
    PubMed     Abstract available


  40. MIYAZAKI M, Tanaka T, Adachi Y, Miya K, et al
    Learning difficulties in Japanese schoolchildren with focal epilepsy.
    Brain Dev. 2020 Jul 2. pii: S0387-7604(20)30168.
    PubMed     Abstract available


    June 2020
  41. YAMAMOTO A, Saito Y, Oyama Y, Watanabe Y, et al
    Effect of total callosotomy on KCNQ2-related intractable epilepsy.
    Brain Dev. 2020 Jun 9. pii: S0387-7604(20)30146.
    PubMed     Abstract available


  42. TAKASE C, Shirai K, Matsumura Y, Watanabe T, et al
    KCNT1-positive epilepsy of infancy with migrating focal seizures successfully treated with nonnarcotic antitussive drugs after treatment failure with quinidine: A case report.
    Brain Dev. 2020 Jun 3. pii: S0387-7604(20)30141.
    PubMed     Abstract available


    May 2020
  43. PAKETCI C, Edem P, Hiz S, Sonmezler E, et al
    Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG.
    Brain Dev. 2020 May 7. pii: S0387-7604(20)30126.
    PubMed     Abstract available


    April 2020
  44. BOONSIMMA P, Suwannachote S, Phokaew C, Ittiwut C, et al
    A case of GABRA5-related developmental and epileptic encephalopathy with response to a combination of antiepileptic drugs and a GABAering agent.
    Brain Dev. 2020 Apr 2. pii: S0387-7604(20)30111.
    PubMed     Abstract available


  45. TAYAMA T, Mori T, Goji A, Toda Y, et al
    Improvement of epilepsy with lacosamide in a patient with ring chromosome 20 syndrome.
    Brain Dev. 2020 Apr 1. pii: S0387-7604(20)30109.
    PubMed     Abstract available


    March 2020
  46. LEE HF, Chi CS, Tsai CR
    Electroclinical variability of pyridoxine-dependent epilepsy caused by ALDH7A1 gene mutations in four Taiwanese children.
    Brain Dev. 2020 Mar 12. pii: S0387-7604(20)30069.
    PubMed     Abstract available


  47. NA JH, Shin S, Yang D, Kim B, et al
    Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy.
    Brain Dev. 2020 Mar 2. pii: S0387-7604(20)30068.
    PubMed     Abstract available


    February 2020
  48. CASH SJ, Mcgue BP, Reynolds TS, Crist ER, et al
    PIGA related disorder as a range of phenotypes rather than two distinct subtypes.
    Brain Dev. 2020;42:205-210.
    PubMed     Abstract available


  49. ENDO W, Ikemoto S, Togashi N, Miyabayashi T, et al
    Phenotype-genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasms.
    Brain Dev. 2020;42:199-204.
    PubMed     Abstract available


  50. INUZUKA LM, Macedo-Souza LI, Della-Ripa B, Cabral KSS, et al
    Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literature.
    Brain Dev. 2020;42:211-216.
    PubMed     Abstract available


  51. HATA Y, Oku Y, Taneichi H, Tanaka T, et al
    Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants.
    Brain Dev. 2020;42:171-178.
    PubMed     Abstract available


  52. SUGITATE R, Okubo Y, Nariai H, Matsui A, et al
    The effects of antihistamine on the duration of the febrile seizure: A single center study with a systematic review and meta-analysis.
    Brain Dev. 2020;42:103-112.
    PubMed     Abstract available


    January 2020
  53. FUJIMOTO A, Okanishi T, Sato K, Itamura S, et al
    Hemispherotomy can cause post-operative strabismus.
    Brain Dev. 2020;42:41-47.
    PubMed     Abstract available


  54. TAKADA R, Tozawa T, Kondo H, Kizaki Z, et al
    Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185T>C variant in the MT-ATP6 gene: Expanding the clinical spectrum.
    Brain Dev. 2020;42:69-72.
    PubMed     Abstract available


  55. TAKEDA K, Miyamoto Y, Yamamoto H, Ishii A, et al
    Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutation.
    Brain Dev. 2020;42:73-76.
    PubMed     Abstract available


    December 2019
  56. HAN JY, Choi SA, Chung YG, Shim YK, et al
    Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS).
    Brain Dev. 2019 Dec 5. pii: S0387-7604(19)30558.
    PubMed     Abstract available


  57. KARATOPRAK E, Tosun O
    Effects of valproic acid and levetiracetam monotherapy on carotid intima-media and epicardial adipose tissue thickness in non-obese children with epilepsy.
    Brain Dev. 2019 Dec 2. pii: S0387-7604(19)30393.
    PubMed     Abstract available


    October 2019
  58. LIANG JS, Huang H, Wang JS, Lu JF, et al
    Phenotypic manifestations between male and female children with CDKL5 mutations.
    Brain Dev. 2019;41:783-789.
    PubMed     Abstract available


    September 2019
  59. KARALOK ZS, Guven A, Ozturk Z, Gurkas E, et al
    Risk factors for recurrence after drug withdrawal in childhood epilepsy.
    Brain Dev. 2019 Sep 11. pii: S0387-7604(19)30261.
    PubMed     Abstract available


  60. MATSUMOTO A, Nagashima M, Iwama K, Mizuguchi T, et al
    Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutation.
    Brain Dev. 2019;41:726-730.
    PubMed     Abstract available


  61. KOSAKA T, Ohta G, Kometani H, Kawatani M, et al
    A case of early myoclonic encephalopathy with intractable seizures successfully treated with high-dose phenobarbital.
    Brain Dev. 2019;41:717-720.
    PubMed     Abstract available


    August 2019
  62. DE RINALDIS M, Giorda R, Trabacca A
    Mild epileptic phenotype associates with de novo eef1a2 mutation: Case report and review.
    Brain Dev. 2019 Aug 30. pii: S0387-7604(19)30367.
    PubMed     Abstract available


  63. KIMURA M, Taketani T, Kurozawa Y
    High incidence of status epilepticus and ongoing seizures on arrival to the hospital due to high prevalence of febrile seizures in Izumo, Japan: A questionnaire-based study.
    Brain Dev. 2019 Aug 12. pii: S0387-7604(19)30279.
    PubMed     Abstract available


  64. DILENA R, De Liso P, Di Capua M, Consonni D, et al
    Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists.
    Brain Dev. 2019;41:595-599.
    PubMed     Abstract available


  65. FUKUI KO, Kubota M, Terashima H, Ishiguro A, et al
    Early administration of vitamins B1 and B6 and l-carnitine prevents a second attack of acute encephalopathy with biphasic seizures and late reduced diffusion: A case control study.
    Brain Dev. 2019;41:618-624.
    PubMed     Abstract available


    July 2019
  66. 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    


  67. 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     Abstract available


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


  69. 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     Abstract available


  70. 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     Abstract available


    May 2019
  71. 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     Abstract available


    April 2019
  72. 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     Abstract available


  73. 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     Abstract available


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


  75. 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     Abstract available


    February 2019
  76. 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     Abstract available


  77. 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    


    January 2019
  78. 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     Abstract available


  79. 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     Abstract available


  80. 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     Abstract available


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


    November 2018
  82. 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     Abstract available


  83. 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     Abstract available


  84. 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     Abstract available


  85. 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     Abstract available


  86. 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     Abstract available


    October 2018
  87. 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     Abstract available


  88. 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     Abstract available


  89. 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     Abstract available


    September 2018
  90. 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     Abstract available


  91. 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     Abstract available


  92. 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     Abstract available


    August 2018
  93. 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     Abstract available


  94. 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     Abstract available


    July 2018
  95. 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     Abstract available


  96. 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     Abstract available


    June 2018
  97. 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     Abstract available


  98. 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     Abstract available


  99. 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     Abstract available


  100. 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     Abstract available


    May 2018
  101. 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     Abstract available


  102. 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     Abstract available


  103. 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     Abstract available


  104. 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     Abstract available


  105. 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     Abstract available


    April 2018
  106. 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     Abstract available


  107. 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     Abstract available


  108. 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     Abstract available


    March 2018
  109. 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     Abstract available


  110. 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     Abstract available


    February 2018
  111. 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     Abstract available


  112. 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     Abstract available


    January 2018
  113. 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     Abstract available


  114. 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    


  115. 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     Abstract available


  116. 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     Abstract available


  117. 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     Abstract available


  118. 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     Abstract available


  119. 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     Abstract available


    December 2017
  120. 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     Abstract available


  121. 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     Abstract available


  122. 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     Abstract available


    November 2017
  123. 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     Abstract available


  124. 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     Abstract available


    October 2017
  125. 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     Abstract available


  126. 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     Abstract available


  127. 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     Abstract available


    September 2017
  128. 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     Abstract available


  129. 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     Abstract available


  130. 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     Abstract available


    August 2017
  131. 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     Abstract available


    July 2017
  132. 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     Abstract available


  133. 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     Abstract available


  134. 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     Abstract available


  135. 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     Abstract available


  136. 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     Abstract available


    May 2017
  137. 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     Abstract available


  138. 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     Abstract available


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


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


    April 2017
  141. 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     Abstract available


  142. 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     Abstract available


  143. 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     Abstract available


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


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


    March 2017
  146. 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     Abstract available


  147. 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     Abstract available


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