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日本小児内分泌学会 | 論文
- Absence of Heterozygous K83E and R257X Mutations of the AIRE-1 Gene in 46 Children with Type 1 Diabetes and 44 Children with Graves' Disease
- Does Urinary Growth Hormone (uGH), Expressed as pg/mg Creatinine, Correlate with Endogenous Growth Hormone (GH) Secretion?
- Growth Hormone Insensitivity Syndrome (GHIS): Clinical Presentation and Effects of Treatment with Recombinant Human Insulin-like Growth Factor I (rhIGF-I) European Experience
- Growth Hormone Treatment in Achondroplasia: 2 Year Results of a Dose-Response Study
- Immunological Changes with Growth Hormone Therapy
- Analysis of Height Velocity in Twenty Girls with Premature Thelarche
- Bone Maturation during Human Growth Hormone (GH) -treated GH Deficient Boys With and Without Gonadal Suppression Treatment
- Transient Hemolysis during Growth Hormone Therapy in Two Patients with Growth Hormone Deficiency
- Transient Hemolysis during Growth Hormone Therapy
- A Case of Hypo-Responsiveness to Thyroid Hormone
- One-year Growth Hormone (GH) Treatment in Children with Non-endocrine Short Stature
- Bone Age Maturation in Children with Non-Endocrine Short Stature (NESS) -Comparison between Tanner-Whitehouse 2 (TW2) Original Method and Standardized TW2 Method for Japanese Children
- Diurnal Variation of Serum Insulin-like Growth Factor Binding Protein-1 in Three Boys and Fasting Insulin-like Growth Factor Binding Protein-1 Levels in Normal Children
- Three-Year Results of Growth Hormone (GH) Treatment in Children with Non-Endocrine Short Stature
- Growth Hormone (GH), Insulin-like Growth Factor I (IGF-I), GH-Binding Protein (GHBP) and Nutritional Improvement in a Girl with Deprivation Syndrome
- Sex Steroid Actions on Epiphyseal Maturation: Evolving New Concepts
- Immunoenhancement through Growth Hormone Treatment
- Increase in Near-Final Height in Short Non-Growth Hormone Deficient Children Treated with Growth Hormone
- Abnormalities of the Pituitary-specific Transcription Factor-1 Gene and Protein
- Growth Hormone Deficiency with Muscular Dystrophy, Arnold-Chiari Malformation Type I and Syringomyelia