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Department Of Pediatrics Hokkaido University School Of Medicine | 論文
- Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
- Prolonged Bone Marrow Failure With Monosomy 7 After Engraftment Failure Following Bone Marrow Transplantation
- Gene Amplification as a Common Cause of lnherted Thyroxine-Binding Globulin Excess: Analysis of One Familial and Two Sporadic Cases
- Effective treatment of cyclic thrombocytopenia with cepharanthin
- 27 A RELATIONSHIP BETWEEN ADIPONECTIN AND SEX HORMONES IN OBESE CHILDREN
- Endocrine Functions in Children with Suprasellar Germinoma
- 内示情報を用いた未達率指標による生産計画システムの提案（II） : ―未達率指標の特性解析と基点在庫方策との比較
- Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
- 内示情報を用いた生産計画システムの分類と活用手順--企業間連携における先行需要情報の活用
- 内示情報を用いた未達率指標による生産計画システムの提案
- Detection of Serum Antibody against Arrestin from Patients with Acute Disseminated Encephalomyelitis
- Measles encephalomyelitis in a patient with a history of vaccination
- Extremely Thickened Media of Small Pulmonary Arteries in Fatal Pulmonary Hypertension With Congenital Heart Disease : A Morphometric and Clinicopathological Study
- A Novel PAX4 Mutation in a Japanese Patient with Maturity-Onset Diabetes of the Young
- Determination of Organophosphorus Pesticides in Biological Samples of Acute Poisoning by HPLC with Diode-Array Detector
- 39 SIBLING CASES OF HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA
- 112 METABOLIC SYNDROME IN SURVIVORS OF CHILDHOOD BRAIN TUMORS WITH ENDOCRINE COMPLICATIONS
- 18 Sporadic haploinsufficiency of the HESX1 gene causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient
- 117 Molecular analysis of PHEX and FGF23 gene in hypophosphatemic rickets
- Impaired GH Secretion due to Prolonged Treatment with Cyproterone Acetate