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Department Of Pediatrics Neonatology And Congenital Disorders Nagoya City University Graduate School | 論文
- 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
- Detection of Hepatitis B Virus DNA by Nested PCR in Serial sera of Infants Born to Hepatitis Be Antigen-Positive Carrier Mothers
- 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
- 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