スポンサーリンク
Department Of Pediatrics Chiba University School Of Medicine | 論文
- Characterization of Genes Encoding the Pancreatic β-cell ATP-sensitive K^+ Channel in Persistent Hyperinsulinemic Hypoglycemia of Infancy in Japanese Patients
- Analyses of Fatal Cases of Kawasaki Disease in Japan Using Vital Statistical Data over 27 Years
- 41 Pseudohypoparathyroidism type Ib with atypical features : the relationship with DNA methylation pattern in XLαs region of GNAS1 gene
- Different patterns of dipole source localization in gelastic seizure with or without a sense of mirth
- Clinical Utility of Thyroid Ultrasonography in the Diagnosis of Congenital Hypothyroidism
- Characterization of children with Mycoplasma pneumoniae infection detected by rapid polymerase chain reaction technique
- Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
- Abnormal DNA synthesis induction in X-ray-irradiated Gorlin fibroblast cells
- Intradural spinal meningioma in a 5-year-old female
- Retrocerebellar arachnoid cysts in siblings with mental retardation and undescended testis
- Empty sella syndrome in nevoid basal cell carcinoma syndrome
- γ-Irradiation Deregulates Cell Cycle Control and Apoptosis in Nevoid Basal Cell Carcinoma Syndrome-derived Cells
- A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible : A case report
- Changes in Glycemic Control and Quality of Life in Pediatric Type 1 Diabetics with Continuous Subcutaneous Insulin Infusion of Insulin Aspart Following Multiple Daily Injection Therapy
- Direct demonstration of humorally mediated inhibition of the transcription of phosphate transporter in XLH patients
- Delirious behavior in influenza is associated with a reversible splenial lesion
- Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
- Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene : a novel source of genomic instability
- Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum
- Fulminant ulcerative colitis associated with both masseter muscle myositis and immunoglobulin M nephropathy