Deletions of mitochondrial DNA (mtDNA) are reported in 19 of 56 patients with mitochondrial myopathy examined in the Department of Neurology and Neuromuscular Research Laboratory, Mayo Clinic, Rochester, MN
Clinical features associated with mtDNA deletions Most patients with chronic progressive external op...
Recent studies have identified a group of patients with cytochrome oxidase (COX) deficiency presenti...
We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among ...
Five children with mitochondrial myopathy associated with depletion of muscle mtDNA are reported fro...
mitochondrial myopathy Abstract—The authors studied seven patients with mitochondrial DNA (mtDNA) my...
Mitochondria are unique among intracellular organelles because they contain their own DNA, which can...
Mitochondria are unique among intracellular organelles because they contain their own DNA, which can...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
Forty per cent of patients with mitochondrial myopathies, a diverse group of multisystem diseases pr...
In situ hybridization combined with immunohistochemical techniques has been applied to study patient...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
We investigated the correlations of deletions of mitochondrial DNA in skeletal muscle with clinical ...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
DELETIONS of muscle mitochondrial DNA (mtDNA) have recently been found in patients with mitochondria...
Clinical features associated with mtDNA deletions Most patients with chronic progressive external op...
Recent studies have identified a group of patients with cytochrome oxidase (COX) deficiency presenti...
We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among ...
Five children with mitochondrial myopathy associated with depletion of muscle mtDNA are reported fro...
mitochondrial myopathy Abstract—The authors studied seven patients with mitochondrial DNA (mtDNA) my...
Mitochondria are unique among intracellular organelles because they contain their own DNA, which can...
Mitochondria are unique among intracellular organelles because they contain their own DNA, which can...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
Forty per cent of patients with mitochondrial myopathies, a diverse group of multisystem diseases pr...
In situ hybridization combined with immunohistochemical techniques has been applied to study patient...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
We investigated the correlations of deletions of mitochondrial DNA in skeletal muscle with clinical ...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
DELETIONS of muscle mitochondrial DNA (mtDNA) have recently been found in patients with mitochondria...
Clinical features associated with mtDNA deletions Most patients with chronic progressive external op...
Recent studies have identified a group of patients with cytochrome oxidase (COX) deficiency presenti...
We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among ...