Background: A deficiency of muscle phosphofructokinase (PFKM) causes a rare metabolic muscle disease, the Tarui disease (Glycogen storage disease type VII, GSD VII) characterized by exercise intolerance with myalgia due to an inability to use glucose as an energy resource. No medical treatment for GSD VII currently exists. The aim of this study was to determine whether a dietary intervention with excessive fat intake would benefit GSD VII.Patient and Methods: A ketogenic diet (KD) intervention implemented as a modified Atkins diet was established for one patient with PFKM deficiency, with a low late lactate response and very high ammonia levels associated with exercise. We recorded the KD intervention for a total of 5 years with clinical an...
HALLER. Abnormal uxidative metabolism and O2 transport in muscle phosphofructokinase deficiency. J. ...
Background: Individuals with glycogen storage disease IIIa (GSD IIIa) (OMIM #232400) experience musc...
Mitochondrial myopathy (MM) with progressive external ophthalmoplegia (PEO) is a common manifestatio...
Background: A deficiency of muscle phosphofructokinase (PFKM) causes a rare metabolic muscle disease...
Introduction: Glycogen storage disease V (GSDV, McArdle disease) and GSDVII (Tarui disease) are the ...
Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by...
Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by...
Glycogen storage disease type IIIa (GSDIIIa) is an inherited disorder of glycogen degradation caused...
Skeletal muscle disorders of glycogenolysis and glycolysis account for most of the conditions collec...
A maladaptive shift from fat to carbohydrate (CHO) oxidation during exercise is thought to underlie ...
Glycogen disease type III (GSDIII), a rare incurable autosomal recessive disorder due to glycogen de...
Patients with glycogen storage disease type V (GSDV), also known as McArdle disease, have blocked gl...
Introduction: Glycogen storage diseases (GSDs) are rare inborn errors of carbohydrate metabolism typ...
BACKGROUND: Movement disorders are a prominent feature of glucose transporter-1 (GLUT1) deficiency s...
HALLER. Abnormal uxidative metabolism and O2 transport in muscle phosphofructokinase deficiency. J. ...
Background: Individuals with glycogen storage disease IIIa (GSD IIIa) (OMIM #232400) experience musc...
Mitochondrial myopathy (MM) with progressive external ophthalmoplegia (PEO) is a common manifestatio...
Background: A deficiency of muscle phosphofructokinase (PFKM) causes a rare metabolic muscle disease...
Introduction: Glycogen storage disease V (GSDV, McArdle disease) and GSDVII (Tarui disease) are the ...
Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by...
Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by...
Glycogen storage disease type IIIa (GSDIIIa) is an inherited disorder of glycogen degradation caused...
Skeletal muscle disorders of glycogenolysis and glycolysis account for most of the conditions collec...
A maladaptive shift from fat to carbohydrate (CHO) oxidation during exercise is thought to underlie ...
Glycogen disease type III (GSDIII), a rare incurable autosomal recessive disorder due to glycogen de...
Patients with glycogen storage disease type V (GSDV), also known as McArdle disease, have blocked gl...
Introduction: Glycogen storage diseases (GSDs) are rare inborn errors of carbohydrate metabolism typ...
BACKGROUND: Movement disorders are a prominent feature of glucose transporter-1 (GLUT1) deficiency s...
HALLER. Abnormal uxidative metabolism and O2 transport in muscle phosphofructokinase deficiency. J. ...
Background: Individuals with glycogen storage disease IIIa (GSD IIIa) (OMIM #232400) experience musc...
Mitochondrial myopathy (MM) with progressive external ophthalmoplegia (PEO) is a common manifestatio...