Goro Takada
Ashikaga Red Cross Hospital(JP)Dokkyo Medical University(JP)
Publications by Year
Research Areas
Congenital Heart Disease Studies, Metabolism and Genetic Disorders, Cardiovascular Function and Risk Factors, Diet, Metabolism, and Disease, Mitochondrial Function and Pathology
Most-Cited Works
- → Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter(1999)557 cited
- → Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene(1993)363 cited
- → De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)(1993)203 cited
- → Genetic Epidemiology of the Carnitine Transporter OCTN2 Gene in a Japanese Population and Phenotypic Characterization in Japanese Pedigrees with Primary Systemic Carnitine Deficiency(1999)177 cited
- → Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy(1990)176 cited
- → Mass production of d-psicose from d-fructose by a continuous bioreactor system using immobilized d-tagatose 3-epimerase(2000)168 cited