Kodama Hiroko | Department Of Community Health And Clinical Epidemiology St. Mary's College

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著作論文

Smoking, drinking, sleeping habits, and other lifestyle factors and the risk of systemic lupus erythematosus in Japanese females : findings from the KYSS study
Role of Prehypertension in the Development of Coronary Atherosclerosis in Japan
Role of Hypertension, Dyslipidemia and Diabetes Mellitus in the Development of Coronary Atherosclerosis in Japan
Expression and Copper-binding Activity of Mammalian Cox17p
Pathophysiology of the transient temporal lobe lesion in a patient with Menkes disease
Copper Metabolism and Copper Transport Disorders
The first reported case of Menkes disease caused by an Alu insertion mutation
Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association
Combination treatment with penicillamine and trientine in a patient with Wilson's disease
Direct Analysis of Ceruloplasmin in Human Blood Serum by HPLC/Inductively Coupled Plasma-Mass Spectrometry for the Diagnosis of Wilson Disease
Prenatal diagnosis of Menkes disease by genetic analysis and copper measurement
Abnormality of vascular elastic fibers in the macular mouse and a patient with Menkes' disease : ultrastructural and immunohistochemical study
Intravenous Arginine Dramatically Improved Hyperammonemia in a Patient with Late-onset Ornithine Transcarbamylase Deficiency
Infantile convulsions with mild gastroenteritis
Genetic Variation in ATP7B Promotor and 5' UTR in Han Chinese Patients with Wilson's Disease
Apolipoprotein E genotype analysis in Chinese Han ethnic children with Wilson's disease, with a concentration on those homozygous for R778L
Transient temporal lobe changes and a novel mutation in a patient with Menkes disease
Molecular genetics and pathophysiology of Menkes disease
Clinical manifestations and treatment of Menkes disease and its variants
Development of antirotavirus agents in Asia
症例報告 Long-term Treatment with High-dose Zinc Sulphate in 36 Children with Wilson's Disease
Cox17p Plays a Key Role for Maintenance of Cellular Copper Homeostasis
Mammalian Cox17p contributes to maintain the cellular and mitochondrial copper homeostasis
Structural and functional analysis of mammalian copper chaperone Cox17p
The Serum Levels of Calcium and Trace Elements in Low Birth Weight Infants
Effective prophylactic therapy for cyclic vomiting syndrome in children using valproate
Genotype-Phenotype Analysis of Mutation R778L in the ATP7B Gene
ヨウ素欠乏による甲状腺機能低下症と経腸栄養剤のヨウ素濃度の検討
Pathology, clinical features and treatments of congenital copper metabolic disorders-Focus on neurologic aspects

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