スポンサーリンク
Department of Pediatrics, Nagoya City University Medical School | 論文
- Interleukin-1β induces the expression of lipocortin 1 mRNA in cultured rat cortical astrocytes
- Cloning of a Rat Glia Maturation Factor-γ (rGMFG) cDNA and Expression of Its mRNA and protein in Rat Organs^1
- Identification and Expression of a Missense Mutation (Y446C) in the Acid Sphingomyelinase Gene from a Japanese Patient with Type A Niemann-Pick Disease
- DOOR syndrome concomitant with non-convulsive status epilepticus and hyperintense cerebellar cortex on T2-Weighted imaging
- Automated determination of 5-fluorouracil and its metabolite in urine by high-performance liquid chromatography with column switching
- Secondary Carnitine Palmitoyltransferase Deficiency in Chronic Renal Failure and Secondary Hyperparathyroidism
- Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug
- Hereditary Orotic Aciduria Heterozygotes Accompanied with Neurological Symptoms
- Noncardiogenic Pulmonary Edema as the Chief Manifestation of a Pheochromocytoma : A Case Report of MEN 2A with Pedigree Analysis of the RET Proto-Oncogene
- 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
- Urinary uracil in female patients with ornithine transcarbamylase 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
- Liquid chromatographic-atmospheric pressure chemical ionization mass spectrometric analysis of glycine conjugates and urinary isovalerylglycine in isovaleric acidemia
- Relationship between Human Cytomegalovirus Glycoprotein B Genotype and Serum Alanine Aminotransferase Elevation in Infants
- Detection of PHKA2 Gene Mutation in Four Japanese Patients with Hepatic Phosphorylase Kinase Deficiency
- TT Virus Infection in Japanese Children : Isolates from Genotype 1 are Overrepresented in Patients with Hepatic Dysfunction of Unknown Etiology
- Detection Rates of TT Virus DNA in Serum of Umbilical Cord Blood, Breast Milk and Saliva
- The Prevalence of Serum GB Virus C/Hepatitis G Virus RNA and Anti-E2 in Japanese Children without a History of Blood Transfusion