Education History
| Fellowship |
Greenwood Genetic Center |
Fellow |
|---|---|---|
| Postdoctoral Fellowship |
University of Oklahoma Health Sciences Center, Department of Biochemistry and Molecular Biology |
Postdoctoral Fellow |
| Doctoral Training |
Federico II University |
PhD |
| Professional Medical |
Federico II University |
MD |
Selected Publications
Journal Article
- De Biase I, Miller M, Zuromski LM, Anderson KJ, Cole SL, Vachali PP, Yuzyuk T (2026). Determination of age-specific reference intervals for ethanolamine plasmalogen species in red blood cells using liquid chromatography tandem mass spectrometry. Clin Chim Acta, 588, 120993.
- Yuzyuk T, McDonald CM, Balogun K, Zuromski LM, De Biase I, Williams N, Meihls S, Asfour F (2026). Persistent plasma and RBC fatty acid abnormalities in children and adolescents with cystic fibrosis on highly effective CFTR modulators. J Cyst Fibros, 25(1), 38-46.
- Duque Lasio ML, Zaitsev M, Hobert JA, De Biase I, Pasquali M, Yuzyuk T (2025). C4OH-carnitine: an important marker of ketosis in patients with and without inborn errors of metabolism. Mol Genet Metab, 145(4), 109160.
- Prinzi J, Pasquali M, Hobert JA, Palmquist R, Wong KN, Francis S, De Biase I (2023). Diagnosing X-Linked Adrenoleukodystrophy after Implementation of Newborn Screening: A Reference Laboratory Perspective. Int J Neonatal Screen, 9(4).
- Yuzyuk T, McDonald CM, Zuromski LM, De Biase I, Johnson L, Williams N, Meihls S, Asfour F (2023). Improvement of lipid and lipoprotein profiles in children and adolescents with cystic fibrosis on CFTR modulator therapy. J Cyst Fibros, 22(6), 1027-1035.
- De Biase I, Yuzyuk T, Cui W, Zuromski LM, Moser AB, Braverman NE (2023). Quantitative analysis of ethanolamine plasmalogen species in red blood cells using liquid chromatography tandem mass spectrometry for diagnosing peroxisome biogenesis disorders. Clin Chim Acta, 542, 117295.
Case Report
- Coody TK, De Biase I, Porter JM, Pasquali M, Shayota BJ (2025). Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism. Mol Genet Metab Rep, 45, 101258.
- De Biase I, de Dios K, Brose SA, Hobert JA (2024). Autism Spectrum Disorder and Mild Developmental Delay in a Patient with a Rare Inborn Error of Metabolism. Clin Chem, 70(6), 882-884.
Abstract
- Cusmano-Ozog K, De Biase I, Cottle B, Young S, Miller M (2026). Interlaboratory performance of amino acid and acylcarnitine quantitation: CAP BGL2 AND BGL4 program findings. [Abstract]. 148(1), 109980.
- Nelson HA, De Biase I, Balogun K, McDonald CM, Meihls S, Asfour F, Yuzyuk T (2023). CFTR Modulator Therapy Increases Plasma Concentrations of Vitamin A in Patients with Cystic Fibrosis [Abstract]. 69(1, Supplement), A-340.
Other
- De Biase I, LoPiccolo M, Thompson L, King M (2026). Introduction to Inborn Errors of Metabolism.