An unusual cytoplasmic organelle of the perineurium in a case of duchenne muscular dystrophy
β Scribed by R. Schober
- Publisher
- Springer-Verlag
- Year
- 1983
- Tongue
- English
- Weight
- 605 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0001-6322
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Twenty-seven boys with Duchenne muscular dystrophy (DMD) entered a double-blind controlled trial of treatment with the calcium antagonist flunarizine. They were matched for age and disability. At monthly intervals, muscle power, functional ability, locomotor score, contractures, and forced vital cap
## Abstract One challenge in the molecular diagnosis of mitochondrial DNA (mtDNA) disorders is detection of a low percentage of mutant heteroplasmy. We report a patient who had a delayed molecular diagnosis of mitochondrial encephalopathy, lactic acidosis, and strokeβlike episodes (MELAS) syndrome