The data from histological, biochemical, and mitochondrial DNA (mtDNA) studies of muscle biopsies from 10 patients affected with chronic progressive external ophthalmoplegia (CPEO) were related to dynamic and metabolic parameters of incremental submaximal exercise. Maximum power output was reduced in all patients as compared to controls. Analysis of the venous lactate curve during exercise revealed a lactate threshold at exercise levels ranging from 40 to 50% of the predicted maximal power output. An earlier significant increase in lactate could be detected by calculating the mean δ lactate. Lactate values were inversely correlated with the cytochrome c oxidase (COX) activity of isolated muscle mitochondria. No relationship was found betwee...
Extraocular muscles are primarily involved in many mitochondrial diseases, but no reports exist rega...
A 25-year-old man complained of progressive diplopia and limb weakness for 3 years. Mitochondrial my...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
The data from histological, biochemical, and mitochondrial DNA (mtDNA ) studies of muscle biopsies f...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
We studied skeletal muscles from eight chronic progressive external ophthalmoplegia patients with ra...
We studied muscle biopsies of 5 patients with Kearns-Sayre syndrome and 3 patients with chronic prog...
Lower limb muscle chronic hyperactivity in hereditary spastic paraplegia (HSP) is the consequence of...
This study quantifies the maior electron microscopic changes in limb muscle biopsies from 31 out of ...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
Chronic Progressive External Opthalmoplegia (CPEO) is the most common phenotypic syndrome of the mit...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
BACKGROUND: Patients with respiratory failure have early fatiguability which may be due to limitatio...
textabstractAims: We wished to demonstrate the feasibility of performing diagnostic mitochondrial DN...
Extraocular muscles are primarily involved in many mitochondrial diseases, but no reports exist rega...
A 25-year-old man complained of progressive diplopia and limb weakness for 3 years. Mitochondrial my...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
The data from histological, biochemical, and mitochondrial DNA (mtDNA ) studies of muscle biopsies f...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
We studied skeletal muscles from eight chronic progressive external ophthalmoplegia patients with ra...
We studied muscle biopsies of 5 patients with Kearns-Sayre syndrome and 3 patients with chronic prog...
Lower limb muscle chronic hyperactivity in hereditary spastic paraplegia (HSP) is the consequence of...
This study quantifies the maior electron microscopic changes in limb muscle biopsies from 31 out of ...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
Chronic Progressive External Opthalmoplegia (CPEO) is the most common phenotypic syndrome of the mit...
Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder cha...
BACKGROUND: Patients with respiratory failure have early fatiguability which may be due to limitatio...
textabstractAims: We wished to demonstrate the feasibility of performing diagnostic mitochondrial DN...
Extraocular muscles are primarily involved in many mitochondrial diseases, but no reports exist rega...
A 25-year-old man complained of progressive diplopia and limb weakness for 3 years. Mitochondrial my...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...