Search Results1-19 of  19

  • SHISHIKURA Keiko ID: 9000001501615

    Department of Pediatrics, Tokyo Women's Medical University, School of Medicine (2009 from CiNii)

    Articles in CiNii:2

    • A 1-year-old infant with McArdle disease associated with hyper-creatine kinase-emia during febrile episodes (2003)
    • Benefits of FK 506 for refractory eye symptoms in a young child with ocular myasthenia gravis (2009)
  • SHISHIKURA Keiko ID: 9000002425790

    Department of Pediatrics, Tokyo Women's Medical University, School of Medicine (2013 from CiNii)

    Articles in CiNii:53

    • Monozygotic Twins with Suspected Hereditary Sensory and Autonomic Neuropathy (HSAN) Type V (1999)
    • A Two-Year-Old Infant with a Myopathic Form of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (2003)
    • Early diagnotic view points in infantile neuroaxonal dystrophy (2003)
  • SHISHIKURA Keiko ID: 9000006635171

    朋診療所 (2012 from CiNii)

    Articles in CiNii:6

    • 小児期をこえた障害者 (1998)
    • Carry Over : Practical Experience of Persons with Severe Motor and Intellectual Disabilities (2005)
    • At the stand of view of the person with severe motor and intellectual disabilities at home and at care home (2012)
  • SHISHIKURA Keiko ID: 9000253305387

    Department of Pediatrics, Tokyo Womens Medical College (1986 from CiNii)

    Articles in CiNii:1

    • Respiratory failure with drastic elevation of serum CPK after the repair of meningomyelocele. (1986)
  • Shishikura Keiko ID: 9000018810008

    Tomo Clinic for Handicapped (2009 from CiNii)

    Articles in CiNii:1

    • Perceptions of the Caregiving Role among Mothers of Children with Severe Motor and Intellectual Disabilities and its Impact on the Mothers' Well-being (2009)
  • Shishikura Keiko ID: 9000255729488

    Department of Pediatrics, Tokyo Women's Medical College (1989 from CiNii)

    Articles in CiNii:1

    • Genetic studies of duchenne muscular dystrophy families using the dystrophin cDNA. (1989)
  • Shishikura Keiko ID: 9000256113266

    Department of Pediatrics, Yokohama City University School of Medicine (1980 from CiNii)

    Articles in CiNii:1

    • A Case of Incontinentia Pigmenti Achromians with Intractable Seizure (1980)
  • Shishikura Keiko ID: 9000256113642

    Departments of Pathology Yokohama City University School of Medicine|Divisions of Pathology Kanagawa Children's Medical Center|Department of Pediatrics, Tokyo Women's Medical College (1982 from CiNii)

    Articles in CiNii:1

    • Neuropathological Study of Werdnig-Hoffmann Disease with Special Remarks on Thalamus and Posterior Roots (1982)
  • Shishikura Keiko ID: 9000256113768

    Department of Pediatrics, Tokyo Women's Medical College (1983 from CiNii)

    Articles in CiNii:1

    • A Histological Study of Mitochondrial Myopathy in Patients Having Partial Deficiency of Pyruvate Dehydrogenase Complex (1983)
  • Shishikura Keiko ID: 9000256113852

    Department of Pediatrics, Tokyo Women's Medical College (1983 from CiNii)

    Articles in CiNii:1

    • Muscle Pathology in a Case of Progressive Myoclonus Epilepsy (Lafora Body Form) (1983)
  • Shishikura Keiko ID: 9000256115357

    Department of Pediatrics, Tokyo Women's Medical College (1988 from CiNii)

    Articles in CiNii:1

    • Home-stay respiratory menagement of a child with nemaline myopathy by means of a negative pressure-controlled respirator. (1988)
  • Shishikura Keiko ID: 9000256115733

    Department of Pediatrics, Tokyo Women's Medical College (1989 from CiNii)

    Articles in CiNii:1

    • Dramatic effects of high-dose intravenous gammaglobulin in each patient with intractable dermatomyositis and polymyositis. (1989)
  • Shishikura Keiko ID: 9000256115808

    Departments of Pediatrics Tokyo Women's Medical College (1990 from CiNii)

    Articles in CiNii:1

    • Skeletal muscle CT scan and ultrasound imaging in two siblings with central core disease. (1990)
  • Shishikura Keiko ID: 9000256116304

    Department of Pediatrics, Tokyo Women's Medical College (1991 from CiNii)

    Articles in CiNii:1

    • Hypothalamic GH Deficiency and Gelastic Seizures in a 10-Year-Old Girl with MELAS. (1991)
  • Shishikura Keiko ID: 9000256118660

    Department of Pediatrics, Tokyo Women's Medical College (1999 from CiNii)

    Articles in CiNii:1

    • Monozygotic Twins with Suspected Hereditary Sensory and Autonomic Neuropathy(HSAN) Type V. (1999)
  • Shishikura Keiko ID: 9000256119880

    Department of Pediatrics, Tokyo Women's Medical University, School of Medicine (2003 from CiNii)

    Articles in CiNii:1

    • A Two-Year-Old Infant with a Myopathic Form of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (2003)
  • Shishikura Keiko ID: 9000256120239

    Tomo Clinic for Handicapped (2005 from CiNii)

    Articles in CiNii:1

    • Child neurologist and medical practice after adolescence Carry Over: Practical Experience of Persons with Severe Motor and Intellectual Disabilities (2005)
  • Shishikura Keiko ID: 9000256852533

    Department of Pediatrics, Tokyo Women's Medical College (1985 from CiNii)

    Articles in CiNii:1

    • Radionuclide study for cardiac lesion in Duchenne muscular dystrophy (1985)
  • Shishikura Keiko ID: 9000402241234

    Tomo-Clinic, Yokohama, Kanagawa (2016 from CiNii)

    Articles in CiNii:1

    • Study on the expectations for the future of their child, and quality of life of mothers of persons with severe motor and intellectual disabilities living at home and related factors. (2016)
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