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Departoment Of Neurology And Geriatrics Kagoshima University Graduate School Of Medical And Dental S | 論文
- The Severity of Minamata Disease Declined in 25 Years : Temporal Profile of the Neurological Findings Analyzed by Multiple Logistic Regression Model
- Clinical Investigation of the Lesions Responsible for Sensory Disturbance in Minamata Disease
- Clinical Course of HTLV-I-Associated Uveitis
- ASSESSMENT OF MITOCHONDRIAL GENE IN PROLIFERATIVE VITREORETINAL TISSUES FROM PATIENTS WITH FAMILIAL DIABETES MELLITUS
- Statistically Significant Differences in the Number of CD24 Positive Muscle Fibers and Satellite Cells between Sarcoglycanopathy and Age-Matched Becker muscular Dystrophy Patients
- Sequence analysis, gene expression, and chromosomal assignment of mouse Borg4 gene and its human orthologue
- LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY : LECTIN HISTOCHEMICAL STUDIES
- Logistic Model Analysis of Neurological Findings in Minamata Disease and the Predicting Index
- Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution
- Facioscapulohumeral Muscular Dystrophy: Clinical Diversity and Genetic Abnormalities in Japanese Patients
- Nationwide Survey of Neurologic Manifestations of Acquired Immunodeficiency Syndrome in Japan
- A Hemophiliac with Human Immunodeficiency Virus (HIV)-1-Associated Dementia Complex
- IMMUNOHISTOCHEMICAL STUDY OF CYTOCHROME C OXIDASE WITH A MONOCLONAL ANTIBODY IN MITOCHONDRIAL MYOPATHY
- Molecular Analysis of Hereditary Deficiency of the Third Component of Complement (C3) in TWO Sisters
- Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant Connexin 32 (GJB1)
- Familial Skeletal Myopathy with Atrioventricular Block
- An Autopsy Case of Peripheral Neuroepithelioma in Posterior Mediastinum with p53 Point Mutation
- Antigenic structures recognized by anti-β2-glycoprotein I auto-antibodies
- Anti-β_2-glycoprotein I antibodies in children with atopic dermatitis
- Immunologic characterization and functional properties of murine antibodies raised against deleted mutants of human β_2-glycoprotein I