Documentos relacionados

1. The Supplement Paradox: Negligible Benefits, Robust Consumption.
2. Molecules interact. But how strong and how much?
3. Long-term complications in classic galactosemia are not progressive.
4. Addition of galactose-1-phosphate measurement enhances newborn screening for classical galactosemia.
5. Galactokinase deficiency: lessons from the GalNet registry.
6. Neonatal classic galactosemia-diagnosis, clinical profile and molecular characteristics in unscreened Turkish population.
7. A multinational study of acute and long-term outcomes of Type 1 galactosemia patients who carry the S135L (c.404C > T) variant of GALT.
8. A novel galactose electrochemical biosensor intended for point-of-care measurement of quantitative liver function using galactose single-point test.
9. A case report of classic galactosemia with a GALT gene variant and a literature review.
10. Classical Hereditary galactosemia: findings in patients and animal models.