Clinical Profiles and Outcomes of the Most Common Inherited Metabolic Diseases in the Philippines: A Review of the National Institutes of Health – Institute of Human Genetics Metabolic Registry
พ.ศ. 2563
ACCURACY OF A POINT-OF-CARE AMMONIA ANALYZER FOR SCREENING OF BLOOD AMMONIA IN PEDIATRIC PATIENTS WITH INBORN ERROR OF METABOLISM
A review of the results of the very long chain fatty acid analyses for X-linked adrenoleukodystrophy at the biochemical genetics laboratory of the institute of human genetics-National Institutes of Health, Manila