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Department Of Neurology Graduate School Of Medical And Pharmaceutical Sciences Kumamoto University | 論文
- Natural Killer Activity and Its Changes among Participants in a Smoking Cessation Intervention Program : a Prospective Pilot Study of 6 Months' Duration
- Severe congestive heart failure with cardiac liver cirrhosis 10 years after orthotopic liver transplantation for familial amyloidotic polyneuropathy
- The Severity of Minamata Disease Declined in 25 Years : Temporal Profile of the Neurological Findings Analyzed by Multiple Logistic Regression Model
- Inhibitory Effect of α-Tocopherol on Methylmercury-Induced Oxidative Steress
- Clinical Investigation of the Lesions Responsible for Sensory Disturbance in Minamata Disease
- Parkinsonian Symptoms as an Initial Manifestation in a Japanese Patient with Acquired Immunodeficiency Syndrome and Toxoplasma Infection
- Statistically Significant Differences in the Number of CD24 Positive Muscle Fibers and Satellite Cells between Sarcoglycanopathy and Age-Matched Becker muscular Dystrophy Patients
- 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
- Complementary Assembly of Heterogenous Peptides into Amyloid Fibrils and Their Catalytic Function
- Comprehensive gene expression profile of human activated T_h1-and T_h2-polarized cells