Galactosemia LB
Speech findings in 13 studies of persons with galactosemia. | Download Table
Galactosemia, a Single Gene Disorder With Epigenetic Consequences | Pediatric Research
Functional analysis of GALT variants found in classic galactosemia patients using a novel cell‐free translation method - Canson - 2019 - JIMD Reports - Wiley Online Library
Screening for galactosemia: is there a place for it? | IJGM
Metabolic Disorders | SpringerLink
Metabolic Disorder | SpringerLink
Galactosemia, a Single Gene Disorder With Epigenetic Consequences | Pediatric Research
pediatrics Flashcards | Quizlet
The natural history of classic galactosemia: lessons from the GalNet registry | Orphanet Journal of Rare Diseases | Full Text
What Is Galactosemia? — Galactosemia Foundation
PDF) Newborn Screening for Galactosemia in the United States: Looking Back, Looking Around, and Looking Ahead
Milk or no milk? Study fills long‑time knowledge gap on babies with genetic disorder – WSU Insider
Galactosemia (GALT deficiency) – newbornscreening.info
Primary ovarian insufficiency in classic galactosemia: current understanding and future research opportunities | SpringerLink
A) Number of male and female cases of galactosemia associated with... | Download Scientific Diagram
Galactosemia causes, symptoms, diagnosis, treatment & galactosemia diet
Galactosemia causes, symptoms, diagnosis, treatment & galactosemia diet
Screening for galactosemia: is there a place for it? | IJGM
Galactosemia case presentation
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
Galactosemia LB
Natural History of Lactic Acidosis after Grand-Mal Seizures — A Model for the Study of an Anion-Gap Acidosis Not Associated with Hyperkalemia | NEJM
Screening for galactosemia: is there a place for it? - Abstract - Europe PMC
