Ukezono N | Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center
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概要
Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center | 論文
- A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17α-Hydroxylase/17m,20-Lyase Deficiency, but without Obvious CYP17 Gene Mutations
- Abnormal steroidogenesis in three patients with Antley-Bixler syndrome : Apparent decreased activity of 17α-hydroxylase, 17,20-lyase and 21-hydroxylase
- Bone Mineral Density and Bone Metabolic Markers in Children with Hyperthyroidism Before and During Treatment