TOGARI Hajime | Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences

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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
Underlying neurologic disorders and recurrence rates of status epilepticus in childhood
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
IS1-04 Oxidative stress subsides by time after living related liver transplantation in pediatric age(Liver and Biliary ductal system,Share Smiles with Sick Children, Dreams and Innovation for Pediatric Surgery)
Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
Bilateral middle cerebral artery infarctions following mild varicella infection : A case report
Nitric oxide further attenuates pulmonary hypertension in magnesium-treated piglets
Nitric oxide inhalation and nitric oxide synthase inhibitor supplement for endotoxin-induced hypotension
A prospective clinical study on inhaled nitric oxide therapy for neonates in Japan
Reduction in cerebral blood flow volume in infants complicated with hypoxic ischemic encephalopathy resulting in cerebral palsy
Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics
Interleukin-1β induces the expression of lipocortin 1 mRNA in cultured rat cortical astrocytes
Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency
Automated determination of 5-fluorouracil and its metabolite in urine by high-performance liquid chromatography with column switching
Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug
Hereditary Orotic Aciduria Heterozygotes Accompanied with Neurological Symptoms
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
Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency
Multiple sclerosis with onset of cerebellar ataxia in an 18-month-old girl
Urinary pyrimidine analysis in healthy newborns, infants, children, adults and patients with congenital metabolic diseases
Vitamin B_6-Responsive Ornithine Aminotransferase Deficiency with a Novel Mutation G237D
Polymorphisms of the Factor VII Gene Associated with the Low Activities of Vitamin K-Dependent Coagulation Factors in One-Month-Old Infants
Detection of PHKA2 Gene Mutation in Four Japanese Patients with Hepatic Phosphorylase Kinase Deficiency
Screening for Pyrimidine Metabolism Disorders Using Dried Filter-Paper Urine Samples : Method Development and a Pilot Study in Nagoya City, Japan
Correlation between Magnetic Resonance Imaging and Clinical Profiles of Periventricular Leukomalacia
National survey of periventricular leukomalacia in Japan
Dopamine penetrates to the central nervous system in developing rats
Optical imaging reveals cation-Cl^- cotransporter-mediated transient rapid decrease in intracellular Cl^- concentration induced by oxygen-glucose deprivation in rat neocortical slices
Unique Electroencephalographic Change of Acute Encephalopathy in Glutaric Aciduria Type 1
Delayed gyration with pontocerebellar hypoplasia type 1
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

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