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Department Of Pediatrics Aichi-gakuin University School Of Pharmacology | 論文
- 85 Congenital Cystic Adenomatoid Malformation(CCAM)の5例
- Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Recurrence of Cushing's Disease after Long-term Remission due to Pituitary Apoplexy
- Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics
- Secondary Carnitine Palmitoyltransferase Deficiency in Chronic Renal Failure and Secondary Hyperparathyroidism
- Effect of Carnitine Administration on Glycine Metabolism in Patients with Isovaleric Acidemia : Significance of Acetylcarnitine Determination to Estimate the Proper Carnitine Dose
- Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug
- 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
- Liquid chromatographic-atmospheric pressure chemical ionization mass spectrometric analysis of glycine conjugates and urinary isovalerylglycine in isovaleric acidemia
- Unique Electroencephalographic Change of Acute Encephalopathy in Glutaric Aciduria Type 1
- Evidence for Remarkable Acylation of Carnitine in Skeletal Muscle of a Neonate with Methylmalonic Aciduria
- A new prenatal diagnosis for methylmalonic aciduria by the assay of propionylcarnitine in amniotic fluid
- 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
- 歯科治療中に初発した症状によってラテックスアレルギーが判明した障害児の1例
- Neonatal alkalemia associated with potential hypovolemia in an infant born to a severely dehydrated mother
- Management of acute metabolic decompensation in maple syrup urine disease : A multi-center study