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日本小児内分泌学会 | 論文
- Guidelines for Diagnosing Steroid 21-Hydroxylase Deficiency
- A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
- Decreased Response to Growth Hormone after Interruption of Therapy
- Insulin-like Growth Factor Binding Protein-3 (IGFBP-3) Measurements in the Diagnosis of Growth Hormone Insufficiency and Comparison with IGF-I Measurements
- Multiple Hormonal Regulation of IGF Binding Protein (IGFBP) -4 in TM-3 Cells
- Clinical Utility of Newly Developed Plasma Free Insulin-like Growth Factor I (IGF-I) Measurements by Immunoradiometric Assay (IRMA) -Preliminary Results in Growth Hormone Deficiency (GHD) Adults and Pregnant Women
- A Novel Mutation of the Steroidogenic Acute Regulatory Protein (StAR) Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
- Spinal and Femoral Bone Mineral Density in Patients with Sexual Precocity, Delayed Adolescence and Hypogonadism: Comparison With Normal Controls
- Octreotide in Acromegaly with Dilated Cardiomyopathy
- Hypoglycemic Effect of Insulin-like Growth Factor II (IGF-II) Is Mediated Mainly through Insulin and/or IGF-I Receptor but not IGF-II Receptor
- Pathogenic Characteristics at Diagnosis in Young Children with Type 1 Diabetes Presenting Prior to 5 Years of Age
- Central Hypothyroidism with Severely Delayed Myelination in a Boy Born to a Mother with Untreated Graves' Disease
- Management Challenges in a Child with Hyperinsulinemic Hypoglycemia
- Severe Failure to Thrive in an Infant Born to a Mother with Albright Hereditary Osteodysplasia (AHO)
- Measurement of Urinary Gonadotropins Using Immuno-fluorometric Assay
- The Effect of Combined Gonadal Suppression and Growth Hormone (GH) Treatment on Bone Maturation in Boys with Non-endocrine Short Stature (NESS)
- Klinefelter Syndrome with Short Stature
- Urinary Excretion of Pyridinoline and Deoxypyridinoline in Children
- Sustained High Insulin-Like Growth Factor-Binding Protein 3 Levels after Suppression of Gonadal Steroids in Central Idiopathic Precocious Puberty
- Molecular Pathology of Congenital Pituitary Hypothyroidism