COLUMBIA PRESBYTERIAN MED CTR, H HOUSTON MERRITT CLIN RES CTR MUSCULAR DYSTROPHY, NEW YORK, NY 10032 USAFED UNIV PARANA, CURITIBA, BRAZILNATL CTR NEUROL & PSYCHIAT, TOKYO, JAPANYESHIVA UNIV ALBERT EINSTEIN COLL MED, BRONX, NY 10461 USAUNIV CALGARY, CALGARY T2N 1N4, ALBERTA, CANADAESCOLA PAULISTA MED, BR-04023 São Paulo, SP, BRAZILHOSP UNIV PENN, PHILADELPHIA, PA 19104 USAUNIV WISCONSIN, MADISON, WI 53706 USAUNIV CATTOLICA SACRO CUORE, I-00168 ROME, ITALYESCOLA PAULISTA MED, BR-04023 São Paulo, SP, BRAZILWeb of Scienc
Single deletions of mitochondrial DNA (mtDNA) are associated with three major clinical conditions: K...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
Progressive external ophthalmoplegia (PEO), Kearns-Sayre syndrome (KSS) and Pearson syndrome are the...
We investigated the correlations of deletions of mitochondrial DNA in skeletal muscle with clinical ...
We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among ...
We studied muscle biopsies of 5 patients with Kearns-Sayre syndrome and 3 patients with chronic prog...
The rapidly expanding list of human diseases due to lesions of mitochondrial DNA includes myopathies...
The phenotypes of Kearns-Sayre syndrome (KSS) and chronic progressive external ophthalmoplegia (CPEO...
Clinical features associated with mtDNA deletions Most patients with chronic progressive external op...
By using a combination of Southern blot hybridization analysis, polymerase–chain reaction amplificat...
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...
Depletion and multiple deletions of mitochondrial DNA (mtDNA) have been associated with a number of ...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
AbstractThe deletions in the mitochondrial DNA from skeletal muscle samples of two oculopharyngeal m...
Single deletions of mitochondrial DNA (mtDNA) are associated with three major clinical conditions: K...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
Progressive external ophthalmoplegia (PEO), Kearns-Sayre syndrome (KSS) and Pearson syndrome are the...
We investigated the correlations of deletions of mitochondrial DNA in skeletal muscle with clinical ...
We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among ...
We studied muscle biopsies of 5 patients with Kearns-Sayre syndrome and 3 patients with chronic prog...
The rapidly expanding list of human diseases due to lesions of mitochondrial DNA includes myopathies...
The phenotypes of Kearns-Sayre syndrome (KSS) and chronic progressive external ophthalmoplegia (CPEO...
Clinical features associated with mtDNA deletions Most patients with chronic progressive external op...
By using a combination of Southern blot hybridization analysis, polymerase–chain reaction amplificat...
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...
Depletion and multiple deletions of mitochondrial DNA (mtDNA) have been associated with a number of ...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
AbstractThe deletions in the mitochondrial DNA from skeletal muscle samples of two oculopharyngeal m...
Single deletions of mitochondrial DNA (mtDNA) are associated with three major clinical conditions: K...
We studied a large family with a dominantly inherited mitochondrial myopathy characterized by progre...
Progressive external ophthalmoplegia (PEO), Kearns-Sayre syndrome (KSS) and Pearson syndrome are the...