スポンサーリンク
Division of Genomics Research, Life Science Research Center, Gifu University | 論文
- Parents of childhood X-linked adrenoleukodystrophy : High risk for depression and neurosis
- Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies
- Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders
- Epidemiology of X-linked adrenoleukodystrophy in Japan
- Urinary organic acids in peroxisomal disorders : a simple screening method
- The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6
- The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil
- Congenital myotonic dystrophy : report of paternal transmission
- Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans
- Prenatal diagnosis of peroxisomal d-3-hydroxyacyl-CoA dehydratase / d-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency
- A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata
- Epilepsy in Peroxisomal Diseases
- Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect
- INCIDENCE OF PEROXISOMAL DISORDERS IN JAPAN
- Natural history of X-linked adrenoleukodystrophy in Japan
- A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) : molecular genetic study
- Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
- Biochemical and Immunocytochemical Properties of Peroxisomes and Mitochondria in Bovine Chromaffin Cells
- X-linked adrenoleukodystrophy : Diagnostic and follow-up system in Japan