SHINAGAWA TAKASHI | Department of Endocrinology and Metabolism, National Research Institute for Child Health and Develop

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著作論文

Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
Japanese Familial Patients with Male-Limited Precocious Puberty
Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
Relationship between Receiving a Workplace Oral Health Examination Including Oral Health Instruction and Oral Health Status in the Japanese Adult Population

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