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日本小児内分泌学会 | 論文
- 137 Transcriptional regulation of 3β-hydroxysteroid dehydrogenase type 2 (3βHSD2)
- 202 Two cases of thyroid disease with atypical initial symptoms
- 106 CLlNICAL DEFINITION OF POLYCYSTIC OVARY SYNDROME(PCOS) IN ADOLESCENCE
- 13 RECENT ADVANCES IN THE TREATMENT OF PEDIATRIC BRAIN TUMORS CONSIDERING ENDOCRINE COMPLICATIONS
- 167 A case of maternal uniparental disomy of chromosome 14 with precocious puberty
- 191 USEFULNESS OF NEW HUMAN TSH RECEPTOR ANTIBODY ASSAY DURING TREATMENT OF GRAVES DISEASE
- 98 DIABETES MELLITUS INDUCED BY HEMOCHROMATOSIS WITH REPEATED BLOOD TRANSFUSION
- 50 ASSOCIATION STUDY OF HUMAN MUT T HOMOLOGUE 1 GENE VAL83MET POLYMORPHISM WITH TYPE 1 DIABETES MELLrrus.
- 206 A CASE OF AUTOIMMUNE THYROIDITIS WITH AUTOIMMUNE HEPATITIS
- 103 A CASE OF SOFT DRINK KETOSIS ASSOCIATED WITH RHBDOMYOLYSIS
- 145 EXPERIENCE OF TREATMENT WITH INSULIN LYSPRO IN PATIENTS WITH TYPE 1 DIABETES MELLITUS
- Insulin-like Growth Factor-1 Polymorphism : Their Physiologic and Clinical Significance
- 212 LOCALIZATION AND PRESENCE OF THYROID CAN BE ASSESSED BY COMPUTED TOMOGRAPHY IN PATIENTS WITH CONGENITAL HYPOTHYROIDSM
- 155 SHOX HAPLOINSUFFICIENCY AND NORMAL OVARIAN FUNCTION VS. SHOX OVERDOSAGE AND GONADAL ESTROGEN DEFICIENCY : LONGITUDINALAUXOLOGICAL STUDY
- 158 TRANSDERMAL DIHYDROTESTOSTERONE TREATMENT FOR THREE PATIENTS WITH STEROID 5α REDUCTASE-2 DEFICIENCY
- 7 GROWTH AND MINERALS : ZINC AND LEAD
- 151 DIABETES MELLITUS As A COMPLICATION OF TREATMENT FOR CHILDREN WITH BLOOD DISORDERS
- 134 DIAGNOSIS OF AN AUTOIMMUNE NEUTROPENIA CASE DURING GROWTH HOERMONE ADMINISTRSTION
- 53 EFFECTS OF MUTANT ALLELES OF THE FORKHEAD TRANSCRIPTION FACTOR Foxo1 ON REGULATION OF HEPATIC INSULIN ACTION AND PANCREATIC β-CELL FUNCTION
- 20 THE IMPORTANCE OF INITIAL EDUCATION FOR JUVENILE-ONSET TYPE 1 DIABETES