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Articles published in
Brain Dev
    September 2022
  1. HASHIMOTO K, Baba S, Nakagawa E, Sumitomo N, et al
    Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report.
    Brain Dev. 2022;44:551-557.
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  2. TAKEDA Y, Sakakibara T, Ogiwara K, Nogami K, et al
    Blood coagulation dynamics during adrenocorticotropic hormone therapy in pediatric patients with infantile spasms.
    Brain Dev. 2022;44:546-550.
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    August 2022
  3. GIACOMINI T, Scala M, Nobile G, Severino M, et al
    De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrum.
    Brain Dev. 2022;44:480-485.
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  4. D'ONOFRIO G, Riva A, Di Rosa G, Cali' E, et al
    Paroxysmal limb dystonias associated with GABBR2 pathogenic variant: A case-based literature review.
    Brain Dev. 2022;44:469-473.
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  5. KOMATSU K, Fukumura S, Minagawa K, Nakashima M, et al
    A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome.
    Brain Dev. 2022;44:474-479.
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    July 2022
  6. SAKATA Y, Nakamura T, Matsuo M
    Reply: Amnestic aphasia in MELAS can be epileptogenic.
    Brain Dev. 2022 Jul 7. pii: S0387-7604(22)00109.
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    June 2022
    Amnestic aphasia in MELAS can be epileptogenic.
    Brain Dev. 2022 Jun 14. pii: S0387-7604(22)00101.
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  8. FUKUOKA M, Kuki I, Hattori Y, Tsuji H, et al
    A case of focal cortical dysplasia type IIa with pathologically suspected bilateral Rasmussen syndrome.
    Brain Dev. 2022;44:401-404.
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  9. KAWAKAMI S, Kubota M, Terashima H, Nagata C, et al
    Differentiating early clinical features of Panayiotopoulos syndrome from acute encephalopathy.
    Brain Dev. 2022;44:386-390.
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    April 2022
  10. IIMURA Y, Nakazawa M, Suzuki H, Mitsuhashi T, et al
    Surgery for intractable epilepsy after severe encephalopathy with reversible splenial lesion and new onset hippocampal lesion associated with parechovirus.
    Brain Dev. 2022 Apr 4. pii: S0387-7604(22)00049.
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    March 2022
  11. OHNO A, Okumura A, Fukasawa T, Nakata T, et al
    Acute encephalopathy with biphasic seizures and late reduced diffusion: Predictive EEG findings.
    Brain Dev. 2022;44:221-228.
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    February 2022
  12. OKANISHI T, Fujii Y, Sakuma S, Shiraishi H, et al
    Lacosamide monotherapy for the treatment of childhood epilepsy with centrotemporal spikes.
    Brain Dev. 2022 Feb 28. pii: S0387-7604(22)00024.
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  13. SAKATA Y, Sano K, Aoki S, Saitsu H, et al
    Neurochemistry evaluated by MR spectroscopy in a patient with SPTAN1-related developmental and epileptic encephalopathy.
    Brain Dev. 2022 Feb 23. pii: S0387-7604(22)00020.
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  14. KIKUCHI K, Hamano SI, Matsuura R, Nonoyama H, et al
    The effectiveness of intravenous benzodiazepine for status epilepticus in Dravet syndrome.
    Brain Dev. 2022 Feb 1. pii: S0387-7604(22)00006.
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  15. JHA R, Kurup A, Kovilapu UB, Ranjan R, et al
    Somatic mutations involving TSC 1 and TSC2 genes in two children with focal cortical dysplasia.
    Brain Dev. 2022;44:166-172.
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  16. GRABER D, Imagawa E, Miyake N, Matsumoto N, et al
    Polymicrogyria in a child with KCNMA1-related channelopathy.
    Brain Dev. 2022;44:173-177.
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  17. MATSUURA R, Hamano SI, Daida A, Horiguchi A, et al
    Serum matrix metallopeptidase-9 and tissue inhibitor of metalloproteinase-1 levels may predict response to adrenocorticotropic hormone therapy in patients with infantile spasms.
    Brain Dev. 2022;44:114-121.
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    January 2022
  18. TAHARA M, Higurashi N, Narita A, Ida H, et al
    Long-term efficacy of low-dose perampanel for progressive myoclonus epilepsy in a patient with Gaucher disease type 3.
    Brain Dev. 2022 Jan 3. pii: S0387-7604(21)00230.
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  19. HADI DA, Mohamed AR, Rethanavelu K, Khoo TB, et al
    Clonic seizures, continuous spikes-and-waves during slow sleep, choreoathetosis and response to sulthiame in a child with FRRS1L encephalopathy.
    Brain Dev. 2022;44:44-49.
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    December 2021
  20. CHEN J, Liu P, Hu W, Shi K, et al
    Absence seizures during sleep in childhood absence epilepsy: A sign of drug resistance?
    Brain Dev. 2021 Dec 9. pii: S0387-7604(21)00213.
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    November 2021
  21. CHAN DL, Rudinger-Thirion J, Frugier M, Riley LG, et al
    A case of QARS1 associated epileptic encephalopathy and review of epilepsy in aminoacyl-tRNA synthetase disorders.
    Brain Dev. 2021 Nov 10. pii: S0387-7604(21)00203.
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  22. NAKAMURA Y, Okanishi T, Yamada H, Okazaki T, et al
    Progressive cerebral atrophies in three children with COL4A1 mutations.
    Brain Dev. 2021;43:1033-1038.
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  23. BOUHADOUN S, Poulin C, Berrahmoune S, Myers KA, et al
    A retrospective analysis of memantine use in a pediatric neurology clinic.
    Brain Dev. 2021;43:997-1003.
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    October 2021
  24. YAMAGUCHI H, Nishiyama M, Tomioka K, Hongo H, et al
    Growth and differentiation factor-15 as a potential prognostic biomarker for status-epilepticus-associated-with-fever: A pilot study.
    Brain Dev. 2021 Oct 27. pii: S0387-7604(21)00187.
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  25. ONO-TAKIGUCHI Y, Muramatsu K, Koshu K, Yamagata T, et al
    Forced normalization of Lennox-Gastaut syndrome using lacosamide: A case report.
    Brain Dev. 2021;43:963-966.
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    September 2021
  26. KIRIKAE H, Uematsu M, Numata-Uematsu Y, Saijo N, et al
    Two types of early epileptic encephalopathy in a Pitt-Hopkins syndrome patient with a novel TCF4 mutation.
    Brain Dev. 2021 Sep 24. pii: S0387-7604(21)00174.
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  27. TAKAMI Y, Nakagawa T
    Risk of seizure recurrence after a first unprovoked seizure in childhood.
    Brain Dev. 2021;43:843-850.
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    August 2021
  28. 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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  29. 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
  30. 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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  31. 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
  32. 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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  33. 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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  34. AZUMAGAWA K, Nakashima I, Kaneko K, Torisu H, et al
    A nation-wide survey of Japanese pediatric MOG antibody-associated diseases.
    Brain Dev. 2021;43:705-713.
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    May 2021
  35. 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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  36. 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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  37. 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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  38. ZHANG Y, Ichinose F, Maeda T, Nakamura T, et al
    A pediatric case of transient periictal MRI abnormalities after repeated seizures.
    Brain Dev. 2021 May 3. pii: S0387-7604(21)00066.
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  39. SUZUKI Y, Ito S, Otani Y, Nishikawa A, et al
    Unexpected elevation in valproic acid concentration and agranulocytosis in a patient with short-chain acyl-CoA dehydrogenase deficiency.
    Brain Dev. 2021;43:657-660.
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  40. IZUMI T, Aihara Y, Kikuchi A, Kure S, et al
    Electroencephalographic findings and genetic characterization of two brothers with IQSEC2 pathogenic variant.
    Brain Dev. 2021;43:652-656.
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  41. YAMAMOTO N, Kuki I, Nagase S, Inoue T, et al
    A case of infantile Tay-Sachs disease with late onset spasms.
    Brain Dev. 2021;43:661-665.
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    April 2021
  42. 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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  43. 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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  44. 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
  45. 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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  46. 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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  47. BATTAGLIA D, Chieffo D, Lucibello S, Marini C, et al
    Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life.
    Brain Dev. 2021;43:419-430.
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  48. KANATANI M, Adachi T, Sakata R, Nishimura Y, et al
    Dravet syndrome with parkinsonian symptoms and intact dopaminergic neurons: A case report.
    Brain Dev. 2021;43:486-489.
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    February 2021
  49. 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.
    >> Share

  50. 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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  51. BAMBORSCHKE D, Kreutzer M, Koy A, Koerber F, et al
    PNPT1 mutations may cause Aicardi-Goutieres-Syndrome.
    Brain Dev. 2021;43:320-324.
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  52. GEIER DA, Geier MR
    A longitudinal cohort study of childhood MMR vaccination and seizure disorder among American children.
    Brain Dev. 2021;43:251-267.
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  53. YOO S, Kim YA, Yoon JY, Seo GH, et al
    The first Korean cases of combined oxidative phosphorylation deficiency 35 with two novel TRIT1 mutations in two siblings confirmed by clinical and molecular investigation.
    Brain Dev. 2021;43:325-330.
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  54. KIM HJ, Yang D, Kim SH, Won D, et al
    Clinical characteristics of KCNQ2 encephalopathy.
    Brain Dev. 2021;43:244-250.
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    January 2021
  55. 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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  56. 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
  57. 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
  58. 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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  59. 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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  60. 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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  61. 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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  62. 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.
    >> Share

  63. 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
  64. 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
  65. 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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  66. 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
  69. 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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  70. 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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  71. 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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  72. 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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  73. 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.
    >> Share

    July 2020
  74. 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.
    >> Share

  75. 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.
    >> Share

  76. 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.
    >> Share

  77. 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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  78. 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.
    >> Share

  79. 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.
    >> Share

  80. 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

  81. 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.
    >> Share

    June 2020
  82. 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.
    >> Share

  83. 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.
    >> Share

    May 2020
  84. 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.
    >> Share

    April 2020
  85. 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.
    >> Share

  86. 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.
    >> Share

    February 2020
  87. 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.
    >> Share

  88. 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

  89. 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

  90. 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.
    >> Share

  91. 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
  92. FUJIMOTO A, Okanishi T, Sato K, Itamura S, et al
    Hemispherotomy can cause post-operative strabismus.
    Brain Dev. 2020;42:41-47.
    >> Share

  93. 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

  94. 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.
    >> Share

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