Nakagawa Masanori | Third Department Of Internal Medicine Kagoshima University Faculty Of Medicine

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概要

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著作論文

An Immunohistochemical Analysis of Gastric B-cell Lymphomas : Stromal Cells Exhibit Peculiar Histogenesis in Gastric B-cell Lymphomas
Severe congestive heart failure with cardiac liver cirrhosis 10 years after orthotopic liver transplantation for familial amyloidotic polyneuropathy
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
Clinical Course of HTLV-I-Associated Uveitis
Statistically Significant Differences in the Number of CD24 Positive Muscle Fibers and Satellite Cells between Sarcoglycanopathy and Age-Matched Becker muscular Dystrophy Patients
Immunohistochemical Analysis of the Pathogenicity of Helicobacter pylori Infection : Excess Nitric Oxide Induced Indirectly by Lewis X and Y is the Cause of the Pathogenicity of Helicobacter pylori Infestation in the Stomach
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
Distribution of Geriatric Disease-Related Genotypes in the National Institute for Longevity Sciences, Longitudinal Study of Aging (NILS-LSA)
Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population
Acid maltase deficiency:clinical, morphological and biochemical observation.
Effects of Stage-matched Repeated Individual Counseling on Smoking Cessation : A Randomized Controlled Trial for the High-risk Strategy by Lifestyle Modification (HISLIM) Study(Special Issue)
Natural Killer Activity and Its Changes among Participants in a Smoking Cessation Intervention Program : a Prospective Pilot Study of 6 Months' Duration

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