スポンサーリンク
Department of Pediatrics, The Jiker university School of Medicine | 論文
- A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene
- Screening for Mutations in the GH-1 Gene by Dideoxy Fingerprinting (ddf)
- Detection of Growth Hormone Gene Defects by Dideoxy Fingerprinting (ddF)
- Successful Intrauterine Therapy for Fetal Goitrous Hypothyroidism during Late Gestation
- Serum glucagon-like peptide-2 levels in neonates : Comparison between extremely low-birthweight infants and normal-term infants
- 11-year-old boy with sarcoidosis and generalized brawny induration of muscle
- A Novel Mutation of the Arginine Vasopressin Receptor 2 Gene in a Patient with Congenital Nephrogenic Diabetes Insipidus
- Pediatric Cerebellar Infarction Caused by Atlantoaxial Subluxation : Case Report
- Peduncular Hallucinosis Associated with Ruptured Basilar-Superior Cerebellar Artery Aneurysm : Case Report