Search Results1-7 of  7

  • Nabatame Shin ID: 9000248198658

    Articles in CiNii:1

    • De novo WDR45 mutation in a patient showing clinically Rett syndrome with childhood iron deposition in brain (2014)
  • Nabatame Shin ID: 9000290355398

    Articles in CiNii:1

    • SPTAN1 encephalopathy : distinct phenotypes and genotypes (2015)
  • NABATAME Shin ID: 9000006352152

    Articles in CiNii:20

    • 3-メチルグルタコン酸尿症の一例 (2004)
    • 若年型クラッベ病に対する造血幹細胞移植の効果 (2005)
    • グルコーストランスポーター1 (Glut-1) 異常症における頭部MRI所見 : 多発性皮質下T_2延長性小病変の経時的検討 (2006)
  • NABATAME Shin ID: 9000016663576

    Department of Pediatrics, Osaka University Graduate School of Medicine (2011 from CiNii)

    Articles in CiNii:2

    • Sleep disordered breathing in childhood-onset acid maltase deficiency (2009)
    • SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome (2011)
  • NABATAME Shin ID: 9000018467764

    Department of Pediatrics, Osaka University (2010 from CiNii)

    Articles in CiNii:1

    • Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis (2010)
  • NABATAME Shin ID: 9000019147875

    Department of Child Neurology, National Center Hospital (NCH), National Center of Neurology and Psychiatry (2011 from CiNii)

    Articles in CiNii:1

    • HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome (2011)
  • Nabatame Shin ID: 9000360597129

    Department of Pediatrics, Osaka University Graduate School of Medicine (2017 from CiNii)

    Articles in CiNii:1

    • Comparison of Silent and Conventional MR Imaging for the Evaluation of Myelination in Children (2017)
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