スポンサーリンク
Department of Pediatrics, Tohoku University School of Medicine | 論文
- Hypospadias in a Male Patient with 21-hydroxylase Deficiency
- Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers(MERRF):a single-photon emission computed tomographic(SPECT)and electrophysiological study
- Functional and Morphological Abnormalities of Mitochondria in Human Cells Containing Mitochondrial DNA with Pathogenic Point Mutations in tRNA Genes
- Tetralogy of Fallot with Absent Pulmonary Valve : Evaluation with Magnetic Resonance Imaging
- Neonatal-Onset Brainstem Reticular Reflex Myoclonus Following a Prenatal Brain Insult : Generalized Myoclonic Jerk and a Brainstem Lesion
- Pulmonary Interstitial Emphysema during Piston-Type High-Frequency Oscillatory Ventilation
- Gastric epithelial cell turnover and mucosal protection in Japanese children with Helicobacter pylori infection
- Comparison between the ^C-urea breath test and stool antigen test for the diagnosis of childhood Helicobacter pylori infection
- Results of triple eradication therapy in Japanese children : a retrospective multicenter study
- Evaluation of Interhemispheric Time Difference by Magnetoencephalography Before and After Total Callosotomy : Two Case Reports
- Abnormal primary somatosensory function in unilateral polymicrogyria : an MEG study
- II D5 Rolandic discharges : comparison between EEG and MEG findings
- Helicobacter pylori and TT virus prevalence in Japanese children
- Disseminated Fusarium Infection Identified by the Immunohistochemical Staining in a Patient with a Refractory Leukemia
- Acid Sphingomyelinase : Relation of ^Lysine Residue on the Ratio of Intracellular to Secreted Enzyme Activity
- Evaluation of Therapeutic Efficacy of Adjuvant Helicobacter pylori Whole Cell Sonicate in Mice with Chronic H. pylori Infection
- Testosterone-Induced Changes in Markers of Bone Turnover in Adolescent Boys with Testicular Dysfunction
- Ultrasonographic Findings in Neonates Screened for Congenital Hypothyroidism
- Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency
- Growth of Two Children after after Six Months Interruption of GH Therapy