Biomolecules | Free Full-Text | A Great Catch for Investigating Inborn Errors of Metabolism—Insights Obtained from Zebrafish
Using a Personal Glucose Meter and Alkaline Phosphatase for Point‐of‐Care Quantification of Galactose‐1‐Phosphate Uridyltransferase in Clinical Galactosemia Diagnosis - Zhang - 2015 - Chemistry – An Asian Journal - Wiley Online Library
Screening for galactosemia: is there a place for it? | IJGM
Developmental Outcomes in Duarte Galactosemia | Pediatrics | American Academy of Pediatrics
Galactosemia by Farshid Mokhberi
PDF] Newborn screening for galactosemia: a review of 5 years of data and audit of a revised reporting approach. | Semantic Scholar
Metabolic Disorders | SpringerLink
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Screening for galactosemia: is there a place for it? | IJGM
Milk or no milk? Study fills long‑time knowledge gap on babies with genetic disorder – WSU Insider
Fragment Screening Reveals Starting Points for Rational Design of Galactokinase 1 Inhibitors to Treat Classic Galactosemia | ACS Chemical Biology
PDF) Language production and working memory in classic galactosemia from a cognitive neuroscience perspective: future research directions | Bernadette Jansma - Academia.edu
Galactosemia : A Genetic Disease of Leloir Pathway | Semantic Scholar