スポンサーリンク
Department Of Neurology Kumamoto University School Of Medicine | 論文
- 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
- Absence of Gallium Uptake in Unicentric and Multicentric Castleman's Disease
- Multicentric Castleman's Disease Manifesting in the Lung : Clinical, Radiographic, and Pathologic Findings and Successful Treatment with Corticosteroid and Cyclophosphamide
- Distribution of Dystrophin and Dystrophin-Associated Protein 43DAG(β-dystroglycan) in the Central Nervous System of Normal Controls and Patients with Duchenne Muscular Dystrophy
- Nitric Oxide Generation from Hydroxyurea via Copper-catalyzed Peroxidation and Implications for Pharmacological Actions of Hydroxyurea
- Bradykinin Generation Triggered by Pseudomonas Proteases Facilitates Invasion of the Systemic Circulation by Pseudomonas aeruginosa
- Expression of constitutively activated EGFRvlll in non-small cell lung cancer
- Nitric Oxide Synthase Activity in Human Lung Cancer
- Familial Multiple Trichoepithelioma Associated With Subclavian-Pulmonary Collateral Vessels and Cerebral Aneurysm
- Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)
- Significant Correlation of Nitric Oxide Synthase Activity and p53 Gene Mutation in Stage I Lung Adenocarcinoma
- Two Cases of Hemiballism-hemichorea with T1-weighted MR Image Hyperintensities in Patients with Hyperglycemia
- Progress of Diagnosis of Acute Stroke
- A Unique Case of Sporadic Creutzfeldt-Jacob Disease Presenting as Progressive Supranuclear Palsy
- Recanalization of the middle cerebral artery after treatment with tissue plasminogen activator in a patient with embolic occlusion detected by transcranial color-flow imaging
- Rapid Screening for Japanese Dysferlinopathy by Fluorescent Primer Extension
- Late onset type I familial amyloidotic polyneuropathy : Presentation of three autopsy cases in comparison with 19 autopsy cases of the ordinary type
- Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan