J Finsterer1. Show Affiliations » 1. fifigs1@yahoo.de
Abstract
Entities: Chemical Disease
Mesh： See more » Carbohydrate Metabolism/physiologyCarbohydrate Metabolism, Inborn Errors/classificationCarbohydrate Metabolism, Inborn Errors/geneticsCarbohydrate Metabolism, Inborn Errors/pathologyFructose-Bisphosphate Aldolase/deficiencyFructose-Bisphosphate Aldolase/geneticsGlycogen/deficiencyGlycogen/metabolismGlycogen Storage Disease Type II/geneticsGlycogen Storage Disease Type II/metabolismGlycogen Storage Disease Type III/geneticsGlycogen Storage Disease Type III/metabolismGlycogen Storage Disease Type IV/geneticsGlycogen Storage Disease Type IV/metabolismGlycogen Storage Disease Type V/geneticsGlycogen Storage Disease Type V/metabolismGlycogen Storage Disease Type VII/geneticsGlycogen Storage Disease Type VII/metabolismGlycogen Storage Disease Type VIII/geneticsGlycogen Storage Disease Type VIII/metabolismHumansL-Lactate Dehydrogenase/deficiencyMitochondrial Myopathies/classificationMitochondrial Myopathies/geneticsMitochondrial Myopathies/pathologyPhosphoglycerate Kinase/deficiencyPhosphoglycerate Mutase/deficiencyPhosphoglycerate Mutase/geneticsPhosphorylase b/deficiency
Substances： See more » GlycogenL-Lactate DehydrogenasePhosphorylase bPhosphoglycerate KinaseFructose-Bisphosphate AldolasePhosphoglycerate Mutase
Year: 2011 PMID： 21989512 DOI： 10.1055/s-0031-1281721
Source DB: PubMed Journal: Fortschr Neurol Psychiatr ISSN： 0720-4299 Impact factor: 0.752