The aim was to identify additional noninvasive tools allowing to detect and to quantify the metabolic impairment in patients with mitochondrial myopathies (MM) or McArdle's disease (McA)
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
AbstractThis paper shows how metabolic control analysis (MCA) can help to explain two important feat...
Patients with mitochondrial myopathies (MM) or myophosphorylase deficiency (McArdle's disease, McA) ...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
Metabolic myopathies are a clinically and etiologically heterogeneous group of disorders due to defe...
Impairment of muscle glycogenolysis in McArdle's disease (myophosphorylase deficiency) leads to exer...
Preface VII Part 3 Muscle Biopsy: Metabolic Diseases 83 Chapter 5Evaluation of mitochondrial fu...
: The relevance of translational medicine (bringing basic science methods "to the bed of patients") ...
Mitochondrial diseases (MD) are disorders caused by impairment of the mitochondrial electron transpo...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
Carbohydrates are the main source of body energy and they can be stored in the organism in form of g...
Abstract Mitochondrial disorders (MDs) are inherited multi‐organ diseases with variable phenotypes. ...
PhD ThesisMitochondrial dysfunction occurs in patients with mitochondrial disease, in neurodegenerat...
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
AbstractThis paper shows how metabolic control analysis (MCA) can help to explain two important feat...
Patients with mitochondrial myopathies (MM) or myophosphorylase deficiency (McArdle's disease, McA) ...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
Metabolic myopathies are a clinically and etiologically heterogeneous group of disorders due to defe...
Impairment of muscle glycogenolysis in McArdle's disease (myophosphorylase deficiency) leads to exer...
Preface VII Part 3 Muscle Biopsy: Metabolic Diseases 83 Chapter 5Evaluation of mitochondrial fu...
: The relevance of translational medicine (bringing basic science methods "to the bed of patients") ...
Mitochondrial diseases (MD) are disorders caused by impairment of the mitochondrial electron transpo...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
Carbohydrates are the main source of body energy and they can be stored in the organism in form of g...
Abstract Mitochondrial disorders (MDs) are inherited multi‐organ diseases with variable phenotypes. ...
PhD ThesisMitochondrial dysfunction occurs in patients with mitochondrial disease, in neurodegenerat...
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
AbstractThis paper shows how metabolic control analysis (MCA) can help to explain two important feat...