Biochemical findings in the first Filipino child confirmed to have nonketotic hyperglycinemia: A case report
พ.ศ. 2559
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
Hematuria, an unusual systemic toxicity, in formic acid ingestion: a case report
Haddad syndrome: A case report in a Filipino infant
พ.ศ. 2560
Clinical presentation of congenital adrenal hyperplasia in selected multiethnic paediatric population
Universiti Putra Malaysia พ.ศ. 2558
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
พ.ศ. 2560
Delayed diagnosis of congenital hypothyroidism in an adolescent results in avoidable complications: a case report
พ.ศ. 2560
Acute intermittent porphyria: A rare cause of hyponatraemia
พ.ศ. 2562
Late infantile neuronal ceroid lipofuscinosis in a Filipino child with epilepsy and progressive neurodegeneration