Kondo Ikuko | Department Of Hygiene Ehime University School Of Medicine

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概要

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著作論文

Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms
Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech
Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome
Polymorphism of the Monocyte Chemoattractant Protein (MCP-1) Gene Is Associated with the Plasma Level of MCP-1 But Not with Carotid Intima-Media Thickness
Effect of Genetic Polymorphism of OATP-C (SLCO1B1) on Lipid-Lowering Response to HMG-CoA Reductase Inhibitors
Classic Rett syndrome in a boy with R133C mutation of MECP2
Characteristic evoked potentials in childhood-onset dentatorubral-pallidoluysian atrophy
Proton magnetic resonance spectroscopy on childhood-onset dentatorubral-pallidoluysian atrophy (DRPLA)
An association of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and common carotid atherosclerosis
An Association between an Antibody against Chlamydia pneumoniae and Common Carotid Atherosclerosis
Angiotensin-Converting Enzyme Gene Deletion Allele Disappear Brachial-Carotid Pulse Pressure Amplification
レビー小体型痴呆症におけるアポリポ蛋白E4型の関与
Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"
Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I
Commentary to the paper entitled 'Non-radioactive DNA diagnosis for the fragile X syndrome in Japanese mentally retarded males' by Nanba et al.
Hypotension Associated with Prone Body Position : A Possible Overlooked Postural Hypotension
The-4,752 C/T Polymorphism in the Presenilin 1 Gene Increases the Risk of Alzheimer's Disease in Apolipoprotein E4 Carriers
Home Blood Pressure Is a Better Predictor of Carotid Atherosclerosis than Office Blood Pressure in Community-Dwelling Subjects
An AciI polymorphism in the 3' untranslated region of the human phosphomannomutase 2 (PMM2) gene
Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms

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