Ito Tetsuya | Department Of Pediatrics Gifu Prefectural Tajimi Hospital

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著作論文

早産児における急性期離脱後一過性循環不全と後期脳室周囲白質軟化症の関係
IL-10 and RANTES are Elevated in Nasopharyngeal Secretions of Children with Respiratory Syncytial Virus Infection
High postnatal oxidative stress in neonatal cystic periventricular leukomalacia
Prevalence and features of migraine in Japanese junior high school students aged 12-15yr
Cardiac Vagal Activation by Adrenocorticotropic Hormone Treatment in Infants with West Syndrome
Periventricular Leukomalacia with Late-Onset Circulatory Dysfunction of Premature Infants : Correlation with Severity of Magnetic Resonance Imaging Findings and Neurological Outcomes
Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
Late circulatory dysfunction and decreased cerebral blood flow volume in infants with periventricular leukomalacia
Reduction in cerebral blood flow volume in infants complicated with hypoxic ischemic encephalopathy resulting in cerebral palsy
The Absolute Number of Peripheral Blood CD34+ Cells Predicts a Timing for Apheresis and Progenitor Cell Yield in Patients with Hematologic Malignancies and Solid Tumors
Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics
Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency
Effect of Carnitine Administration on Glycine Metabolism in Patients with Isovaleric Acidemia : Significance of Acetylcarnitine Determination to Estimate the Proper Carnitine Dose
Evaluation of Hematological Reconstitution Potential of Autologous Peripheral Blood Progenitor Cells Cryopreserved by a Simple Controlled-Rate Freezing Method
A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy
Long follow up of betaine therapy in two Japanese siblings with cystathionine β-synthase deficiency
Novel mutations in the cytochrome P450 2C19 gene : a pitfall of the PCR-RFLP method for identifying a common mutation
A Simple Quantitative Assay for Urinary Adenosine Using Column-Switching High-Performance Liquid Chromatography
Urinary uracil in female patients with ornithine transcarbamylase deficiency
Multiple sclerosis with onset of cerebellar ataxia in an 18-month-old girl
Vitamin B_6-Responsive Ornithine Aminotransferase Deficiency with a Novel Mutation G237D
Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy : Two sibling cases
Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency : A case report
Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis
Determination of 3-hydroxyisovalerylcarnitine and other acylcarnitine levels using liquid chromatography-tandem mass spectrometry in serum and urine of a patient with multiple carboxylase deficiency

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