Search Results1-6 of  6

  • KUWAJIMA Katsuko ID: 9000000395724

    Department of Pediatrics, Ibaraki Handicapped Children's Hospital, Mito, Ibaraki (FM, KK, KY) (2001 from CiNii)

    Articles in CiNii:7

    • Natutal History of Japanese Williams Syndrome in Childhoob (1997)
    • Clinical Study of Ten Patients with Angelman Syndrome (1997)
    • Gene Analysis of the Neural Cell Adhesion Molecule L1 (L1CAM) in a Japanese Family with X-linked Hydrocephalus (1997)
  • KUWAJIMA Katsuko ID: 9000000608094

    Department of Pediatrics, Ibaraki Handicapped Children's Hospital (1999 from CiNii)

    Articles in CiNii:3

    • Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I (1999)
    • An AciI polymorphism in the 3' untranslated region of the human phosphomannomutase 2 (PMM2) gene (1999)
    • Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms (1998)
  • KUWAJIMA Katsuko ID: 9000001460315

    Department of Pediatrics, Ibaraki Prefectural Handicapped Children's Center (2005 from CiNii)

    Articles in CiNii:1

    • Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms (2005)
  • KUWAJIMA Katsuko ID: 9000001709919

    Department of Pediatrics, Ibaraki Handicapped Children's Hospital (2005 from CiNii)

    Articles in CiNii:1

    • A pediatric case of critical illness polyneuropathy : clinical and pathological findings (2005)
  • KUWAJIMA Katsuko ID: 9000255730733

    Kanagawa Children's Medical Center, Yokohama, Kanagawa (1974 from CiNii)

    Articles in CiNii:1

    • A Hydrocephalic Girl with Progressive Muscular Dystrophy: A case report (1974)
  • Kuwajima Katsuko ID: 9000256119168

    Department of Pediatrics, Ibaraki Handicapped Children's Hospital (2001 from CiNii)

    Articles in CiNii:1

    • A Case of Bilateral Coronal Craniosynostosis with the P250R Mutation in FGFR3 Gene. (2001)
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