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Articles published in
Brain Dev
    August 2021
  1. KASHIKI T, Kido J, Momosaki K, Kusunoki S, et al
    Mitochondrial DNA depletion syndrome with a mutation in SLC25A4 developing epileptic encephalopathy: A case report.
    Brain Dev. 2021 Aug 25. pii: S0387-7604(21)00155.
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  2. ICHINOSE F, Nakamura T, Kira R, Furuno K, et al
    Incidence and risk factors of acute encephalopathy with biphasic seizures in febrile status epilepticus.
    Brain Dev. 2021 Aug 3. pii: S0387-7604(21)00132.
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    July 2021
  3. TAIRA R, Yamamura K, Maeda T, Sakata A, et al
    Paroxysmal sympathetic hyperactivity and the later development of epilepsy in a chemotherapy-associated brain damage.
    Brain Dev. 2021 Jul 20. pii: S0387-7604(21)00129.
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  4. 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.
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    June 2021
  5. 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.
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  6. 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.
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    May 2021
  7. 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.
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  8. 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.
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  9. 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.
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    April 2021
  10. 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.
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  11. 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.
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  12. 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.
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    March 2021
  13. 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.
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  14. 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.
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    February 2021
  15. 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.
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  16. 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.
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    January 2021
  17. 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.
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  18. 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.
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    December 2020
  19. 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.
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    November 2020
  20. 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.
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  21. 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.
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  22. 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.
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  23. 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.
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  24. 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.
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  25. 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.
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    October 2020
  26. 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.
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    September 2020
  27. 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.
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  28. 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.
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    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.
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    Epilepsy in Angelman syndrome: A scoping review.
    Brain Dev. 2020 Sep 3. pii: S0387-7604(20)30240.
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    August 2020
  31. 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.
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  32. 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.
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  33. 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.
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  34. 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.
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  35. 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.
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    July 2020
  36. 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.
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  37. 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.
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  38. 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.
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  39. 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.
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  40. 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.
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  41. 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.
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  42. 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.
    >> Share

  43. 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.
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    June 2020
  44. 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.
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  45. 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.
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    May 2020
  46. 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.
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    April 2020
  47. 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.
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  48. 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.
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    March 2020
  49. 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.
    >> Share

  50. 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.
    >> Share

    February 2020
  51. 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.
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  52. 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.
    >> Share

  53. 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.
    >> Share

  54. 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.
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  55. 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.
    >> Share

    January 2020
  56. FUJIMOTO A, Okanishi T, Sato K, Itamura S, et al
    Hemispherotomy can cause post-operative strabismus.
    Brain Dev. 2020;42:41-47.
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  57. 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.
    >> Share

  58. 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.
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    December 2019
  59. 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.
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  60. 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.
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    October 2019
  61. 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.
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    September 2019
  62. 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.
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  63. 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.
    >> Share

  64. 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.
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    August 2019
  65. 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.
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  66. 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.
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  67. 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.
    >> Share

  68. 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.
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    July 2019
  69. 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.
    >> Share

  70. 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.
    >> Share

    June 2019
  71. KAMATE M, Detroja M, Hattiholi V
    Neuronal ceroid lipofuscinosis type-11 in an adolescent.
    Brain Dev. 2019;41:542-545.
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  72. 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.
    >> Share

  73. 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.
    >> Share

    May 2019
  74. 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.
    >> Share

    April 2019
  75. 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.
    >> Share

  76. 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.
    >> Share

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

  78. 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.
    >> Share

    February 2019
  79. 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.
    >> Share

  80. 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.
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    January 2019
  81. 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.
    >> Share

  82. 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.
    >> Share

  83. 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.
    >> Share

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

    November 2018
  85. 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.
    >> Share

  86. 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.
    >> Share

  87. 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.
    >> Share

  88. 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.
    >> Share

  89. 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.
    >> Share

    October 2018
  90. 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.
    >> Share

  91. 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.
    >> Share

  92. 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.
    >> Share

    September 2018
  93. 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.
    >> Share

  94. 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.
    >> Share

  95. 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.
    >> Share

    August 2018
  96. 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.
    >> Share

  97. 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.
    >> Share

    July 2018
  98. 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.
    >> Share

  99. 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.
    >> Share

    June 2018
  100. 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.
    >> Share

  101. 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.
    >> Share

  102. 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.
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  103. 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.
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    May 2018
  104. 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.
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  105. 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.
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  106. 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.
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  107. 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.
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  108. 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.
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    April 2018
  109. 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.
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  110. 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.
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  111. 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.
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    March 2018
  112. 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.
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  113. 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.
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    February 2018
  114. 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.
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  115. 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.
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    January 2018
  116. 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.
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  117. 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.
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  118. 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.
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  119. 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.
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  120. 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.
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  121. SPAGNOLI C, Salerno GG, Iodice A, Frattini D, et al
    KCNQ2 encephalopathy: A case due to a de novo deletion.
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  122. KOJIMA K, Shirai K, Kobayashi M, Miyauchi A, et al
    A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation.
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    December 2017
  123. 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.
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  124. 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.
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  125. 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.
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    November 2017
  126. 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.
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  127. 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.
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    October 2017
  128. 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.
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  129. 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.
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  130. 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.
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    September 2017
  131. 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.
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  132. 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.
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  133. 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.
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    August 2017
  134. 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.
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    July 2017
  135. 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.
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  136. 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.
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  137. 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.
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  138. 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.
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  139. 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.
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    May 2017
  140. 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.
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  141. 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.
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  142. ISIK U, Dincer A
    Central tegmentum tract hyperintensities in pediatric neurological patients: Incidence or coincidence.
    Brain Dev. 2017;39:411-417.
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  143. NUMOTO S, Kurahashi H, Azuma Y, Numaguchi A, et al
    Fournier's gangrene during ACTH therapy.
    Brain Dev. 2017;39:435-438.
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    April 2017
  144. 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.
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  145. 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.
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  146. 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.
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  147. GROSSO S, Ferranti S, Gaggiano C, Grande E, et al
    Massive lamotrigine poisoning. A case report.
    Brain Dev. 2017;39:349-351.
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  148. MASRI A, Chung SK, Rees MI
    Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patients.
    Brain Dev. 2017;39:306-311.
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    March 2017
  149. KIZTANIR H, Bektas G, Yildiz EP, Uzunhan TA, et al
    Coexisting neuronal autoantibodies among children with demyelinating syndromes.
    Brain Dev. 2017;39:248-251.
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  150. 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.
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