Search Results1-5 of  5

  • Kijima Kazuki ID: 9000010064865

    Articles in CiNii:1

    • Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy (2005)
  • Kijima Kazuki ID: 9000014312504

    Articles in CiNii:1

    • Temporary Hyperbilirubinemia in Two Patients During Treatment for Idiopathic Nephrotic Syndrome (2004)
  • KIJIMA KAZUKI ID: 9000001234889

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

    Articles in CiNii:5

    • Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome (2004)
    • Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease (2004)
    • Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese (2005)
  • KIJIMA Kazuki ID: 9000001460571

    Department of Pediatrics, Yamagata University School of Medicine (2005 from CiNii)

    Articles in CiNii:3

    • A pedigree of Charcot-Marie-Tooth disease type 4F (Periaxin mutation) (2005)
    • Charcot-Marie-Tooth 病2A型におけるミトコンドリア GTPase Mitofusin 2 遺伝子異常について (2004)
    • Charcot-Marie-Tooth 病および Distal hereditary motor neuropathy におけるHSP22および27遺伝子異常について (2005)
  • Kijima Kazuki ID: 9000257870330

    Departments of Pediatrics, Yamagata University School of Medicine (2004 from CiNii)

    Articles in CiNii:1

    • Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome (2004)
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