The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in Children. [PDF]
Lipiński P, Doroba A.
europepmc +1 more source
Pompe Disease: Pathogenesis, Molecular Mechanisms, Neurological Aspects, Diagnostics and Modern Therapeutic Approaches. [PDF]
Sharshakova A +6 more
europepmc +1 more source
Genetic diagnosis of Jordanian patients with glycogen storage diseases. [PDF]
Shboul M, El-Khateeb M, Fathallah R.
europepmc +1 more source
Untargeted Proteomics Profiling of Liver and Plasma in Fed and Fasted Liver-Specific Glycogen Storage Disease Type Ia (GSD Ia) Mice: Toward Potential Protein Biomarkers. [PDF]
Xiao R +7 more
europepmc +1 more source
Population Pharmacokinetic/Pharmacodynamic Modeling of Therapeutic Enzymes in Lysosomal Storage Diseases. [PDF]
Barzel I +5 more
europepmc +1 more source
An overview on cardiac involvement in Inborn Errors of Metabolism: from clinical clues to nutritional management strategies. [PDF]
Montanari C +10 more
europepmc +1 more source
Growth impairment in glycogen storage disease type I versus types III/VI/IX: a cross-sectional study. [PDF]
Wu X, Sun Y, Yang M.
europepmc +1 more source
Impact of COVID-19 infection in patients with inherited metabolic diseases: a National Multicenter Study from the French IMDs Healthcare Network for Rare Diseases. [PDF]
Douillard C +24 more
europepmc +1 more source

