Search Results1-20 of  72

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  • Kenzo TAKESHITA ID: 9000400052607

    Articles in CiNii:1

    • Etiology and prevention of cerebral palsy : Central nervous system and congenital malformations (1971)
  • Kenzo TAKESHITA ID: 9000400063106

    Articles in CiNii:1

    • Hypotryptophanemia with Tryptophan Malabsorption and Agenesis of the Septum Pellucidum in Two Siblings (1976)
  • Kenzo TAKESHITA ID: 9000400095970

    Articles in CiNii:2

    • Sister Chromatid Exchanges, Chromosome Aberration and Lymphocyte Proliferative Kinetics in Non-treated and MNNG-treated Lymphocytes from Patients with Tuberous Sclerosis (1984)
    • Children of Epileptic and Psychotic Mothers (1985)
  • Kenzo TAKESHITA ID: 9000400096181

    Articles in CiNii:1

    • Monitoring of Congenital Malformations in Tottori, 1974-1983 (1984)
  • TAKESHITA KENZO ID: 9000001742595

    Division of Child Neurology, Institute of Neurological Sciences (2000 from CiNii)

    Articles in CiNii:1

    • Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion (2000)
  • TAKESHITA Kenzo ID: 9000000435927

    Division of Child Neurology, Department of Neurobiology, School of Life Sciences, Faculty of Medicine, Tottori University (1995 from CiNii)

    Articles in CiNii:1

    • Carbohydrate-deficient glycoprotein syndrome : electrophoretic study of multiple serum glycoproteins (1995)
  • TAKESHITA Kenzo ID: 9000000436187

    Division of Child Neurology,Institute of Neurological Sciences,Faculty of Medicine,Tottori University (1995 from CiNii)

    Articles in CiNii:1

    • Bilateral opercular syndrome: an unusyal complication of perinatal difficulties (1995)
  • TAKESHITA Kenzo ID: 9000000436345

    Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori Yniversity, Yonago 683-8503, Japan (1999 from CiNii)

    Articles in CiNii:6

    • Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males (1995)
    • Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers (1996)
    • Pontine hypoplasia in a child with sensorineural deafiness (1997)
  • TAKESHITA Kenzo ID: 9000000436362

    Division of Child Neurology, Institute of Neurological Sciences, Tottori University School of Medicine (1995 from CiNii)

    Articles in CiNii:1

    • Frequency of the Prader-Willi syndrome in the San-in district, Japan (1995)
  • TAKESHITA Kenzo ID: 9000000436905

    Division of Child Neurology, Institute of Neurological Sciences, Tottori University School of Medicine (1997 from CiNii)

    Articles in CiNii:2

    • Sensorineural deafness in siblings with adenosine deaminase deficiency (1996)
    • Intracraninal calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report (1997)
  • TAKESHITA Kenzo ID: 9000000437186

    Division of Neurology, ustitute of Neurological sciences, Faculty of Medicine, Tottori University (1997 from CiNii)

    Articles in CiNii:1

    • Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case (1997)
  • TAKESHITA Kenzo ID: 9000000457722

    Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University (1998 from CiNii)

    Articles in CiNii:1

    • A case report of remarkable improvement of motor disturbances with _L-dopa in a patient with post-diffuse axonal injury (1998)
  • TAKESHITA Kenzo ID: 9000000491549

    Division of Child Neurology, Institute of Neurological Sciences, Tottori University School of Medicine (1992 from CiNii)

    Articles in CiNii:1

    • A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease (1992)
  • TAKESHITA Kenzo ID: 9000000607647

    Division of Child Neurological, Institute of Neurology Sciences, Faculty of Medicine, Tottori University (1998 from CiNii)

    Articles in CiNii:1

    • Slowly progressive cystic leukoencephalopathy with megalencephaly in a Japanese boy (1998)
  • TAKESHITA Kenzo ID: 9000000608051

    Division of Child Neurology, Institute of Neurological Science, Tottori University Faculty of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis (1999)
  • TAKESHITA Kenzo ID: 9000000830655

    Division of Child Neurology, Institute of Neurological Sciences, Tottori University School of Medicine (1997 from CiNii)

    Articles in CiNii:1

    • IgA and IgG2 Deficiency Associated with Zonisamide Therapy: A Case Report (1997)
  • TAKESHITA Kenzo ID: 9000000929667

    Department of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University (2001 from CiNii)

    Articles in CiNii:1

    • A Japanese girl with leukoencephalopathy with vanishing white matter (2001)
  • TAKESHITA Kenzo ID: 9000000930352

    Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University (2002 from CiNii)

    Articles in CiNii:1

    • Unilateral occlusion of the middle cerebral artery after varicella-zoster virus infection (2002)
  • TAKESHITA Kenzo ID: 9000001075922

    Division of Child Neurology, Institute of Neurological Sciences, Tottori University School of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan (1999)
  • TAKESHITA Kenzo ID: 9000001078583

    Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University (2001 from CiNii)

    Articles in CiNii:1

    • Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X (2001)
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