スポンサーリンク
Department Of Pediatrics Hokkaido University School Of Medicine | 論文
- Studies of Very Severe Short Stature with Severe GH Deficiency : From the Data Registered with the Foundation for Growth Science
- Serum Levels of 20-Kilodalton Human Growth Hormone (GH) in Children with Simple Obesity
- The Comparison of the Effects of Short-Term Growth Hormone Treatment in Patients with Achondroplasia and with Hypochondroplasia
- Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children ; Relations to Total IGF-I, IGF Binding Protein (IGFBP)-1, IGFBP-3, and Acid Labile Subunit (ALS)
- Elevated serum levels of soluble interleukin-2 receptor in juvenile dermatomyositis
- Insulin-Like Growth Factors (IGFs) and IGF-Binding Proteins (IGFBP-1, -2 and -3) in Diabetic Pregnancy:Relationship to Macrosomia
- Elevated Serum Bisphenol A Levels under Hyperandrogenic Conditions may be Caused by Decreased UDP-glucuronosyltransferase Activity
- Differences in Serum Bisphenol A Concentrations in Premenopausal Normal Women and Women with Endometrial Hyperplasia
- A Case of Female Pseudohermaphroditism Caused by Aromatase Deficiency
- Viriizing Adrenocortical Carcinoma Invading the Right Atrium with Histological High-Grade Malignancy and p53 Mutation in a 3-Year-Old Child : Indication of Post Operative Adjuvant Chemotherapy
- Disorders of the Hypothalamic-Pituitary-Adrenal Axis Caused by Overdosed Anti-Allergic Drug : A Case Report
- A Ten-Year Old Male with Bromocriptine Resistant PRL and GH-Producing Huge Pituitary Adenoma
- Growth Hormone (GH) Binding Protein in Children with Intrauterine Growth Retardation Treated with High Dose GH
- Japanese Familial Patients with Male-Limited Precocious Puberty
- Genetic and Endocrinological Evaluations of Three 46, XX Patients with Congenital Lipoid Adrenal Hyperplasia Previously Reported as Having Presented Spontaneous Puberty
- Final Height in Girls with Turner Syndrome after Growth Hormone Treatment ; Experience at National Children's Hospital
- Two Children with Xanthogranuloma of the Sellar Region
- Familial hypomagnesemia with hypercalciuria and nephrocalcinosis : unusual clinical associations and novel claudin16 mutation in an Egyptian family
- A Novel V2 Vasopressin Receptor Mutation with X-Linked Nephrogenic Diabetes Insipidus
- Two Japanese Patients with Gitelman Syndrome