スポンサーリンク
Department of Pediatrics, Jichi Medical University School of Medicine | 論文
- Diagnosis of Arteriovenous Malformation of the Internal Iliac Vessels by Color Doppler Ultrasonography : A Case Report
- Ehlers-Danlos type IV in pregnancy with a history of myocardial infarction
- Differential T-cell response in a young child and neonates with toxic shock syndrome
- Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy
- Elevated CSF IL-6 in a patient with respiratory syncytial virus encephalopathy
- 特発性ステロイド感受性ネフローゼ症候群にMIP-1βとIL-8は関与する
- Volume measurement of a pediatric ventricular phantom model using three-dimensional echocardiography
- Volume Measurement of Small Ventricular Model by Real-time Three-dimensional Echocardiography
- Efficacy of Iodine-123-15-(p-iodophenyl)-3-R, S-Methylpentadecanoic Acid Single Photon Emission Computed Tomography Imaging in Detecting Myocardial Ischemia in Children With Kawasaki Disease
- Inhalation of nebulized nitroglycerin in dogs with experimental pulmonary hypertension induced by U46619
- Progressive Infundibular Stenosis after Balloon Pulmonary Valvuloplasty in Pulmonary Atresia with Intact Ventricular Septum in An Infant Who Underwent Brock Operation
- Sequential Interventional Cardiac Catheterization Treatment of Combined Coarctation of the Aorta and Patent Ductus Arteriosus
- Autonomic Function in Adolescents with Orthostatic Dysregulation Measured by Heart Rate Variability
- Autonomic function in Kawasaki disease with myocardial infarction : Usefulness of monitoring heart rate variability
- Expression analysis and mutation detection of DLX5 and DLX6 in autism
- Colonization process of the root endophytic fungus Heteroconium chaetospira in roots of Chinese cabbage
- Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay-Sachs disease
- Mutation analysis of methyl-CpG binding protein family genes in autistic patients
- Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
- RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes