Objective. To investigate the ratios of creatine kinase (CK) to aminotransferases as biomarkers of acute liver injury in dystrophinopathy. Methods. C57 and mdx (dystrophic) mice were treated with a hepatotoxic reagent D-galactosamine (D-GalN). The degrees of liver and muscle injury were assessed using histological examinations. To examine whether serum CK-adjusted aminotransferase levels could indicate liver status in dystrophic mice, the CK/alanine aminotransferase (ALT) and CK/aspartate aminotransferase (AST) ratios were analyzed. Furthermore, we enrolled 658 male patients with dystrophinopathy and 378 male patients without muscle and liver injury as control, whose serum ALT, AST, and CK levels were examined. Results. Animal experiments i...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
International audienceDystrophin absence in Duchenne muscular dystrophy (DMD) causes severe muscle d...
Serum Creatine Kinase analysis in mouse models of muscular dystrophy. SOP (ID) Number MD_M.2.2.001 V...
Serum activities of alanine and aspartate aminotransferases (ALT and AST) are used as gold standard ...
Five male children are reported in whom incidental recognition of elevated serum alanine aminotransf...
Creatine kinase (CK, EC 2.7.3.2) assays usually contain thiol-reducing compounds to restore the enzy...
BACKGROUND: Duchenne muscular dystrophy (DMD) consists of a lack in the expression of the subsarcole...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
Duchennen lihasdystrofia (engl. Duchenne muscular dystrophy, DMD) on lähes pelkästään pojilla ilmene...
Background: Duchenne muscular dystrophy is a highly complex multi-system disease caused by primary a...
Purpose: Histone Deacetylase inhibitors (DI) ameliorates dystrophic muscle regeneration restoring mu...
Serum creatine kinase (CK) was first used as a diagnostic aid in progressive muscular dystrophy in 1...
Abstract Background Duchenne muscular dystrophy is a highly complex multi-system disease caused by p...
BACKGROUND: Many muscular dystrophies currently remain untreatable. Recently, dietary ribitol has be...
BACKGROUND: Many muscular dystrophies currently remain untreatable. Recently, dietary ribitol has be...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
International audienceDystrophin absence in Duchenne muscular dystrophy (DMD) causes severe muscle d...
Serum Creatine Kinase analysis in mouse models of muscular dystrophy. SOP (ID) Number MD_M.2.2.001 V...
Serum activities of alanine and aspartate aminotransferases (ALT and AST) are used as gold standard ...
Five male children are reported in whom incidental recognition of elevated serum alanine aminotransf...
Creatine kinase (CK, EC 2.7.3.2) assays usually contain thiol-reducing compounds to restore the enzy...
BACKGROUND: Duchenne muscular dystrophy (DMD) consists of a lack in the expression of the subsarcole...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
Duchennen lihasdystrofia (engl. Duchenne muscular dystrophy, DMD) on lähes pelkästään pojilla ilmene...
Background: Duchenne muscular dystrophy is a highly complex multi-system disease caused by primary a...
Purpose: Histone Deacetylase inhibitors (DI) ameliorates dystrophic muscle regeneration restoring mu...
Serum creatine kinase (CK) was first used as a diagnostic aid in progressive muscular dystrophy in 1...
Abstract Background Duchenne muscular dystrophy is a highly complex multi-system disease caused by p...
BACKGROUND: Many muscular dystrophies currently remain untreatable. Recently, dietary ribitol has be...
BACKGROUND: Many muscular dystrophies currently remain untreatable. Recently, dietary ribitol has be...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
International audienceDystrophin absence in Duchenne muscular dystrophy (DMD) causes severe muscle d...
Serum Creatine Kinase analysis in mouse models of muscular dystrophy. SOP (ID) Number MD_M.2.2.001 V...