Cardiomyopathy in Friedreich Ataxia: Clinical Findings and Research
β Scribed by Payne, R. M.; Wagner, G. R.
- Book ID
- 111924979
- Publisher
- SAGE Publications
- Year
- 2012
- Tongue
- English
- Weight
- 589 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0883-0738
No coin nor oath required. For personal study only.
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## Abstract Dysarthria in Friedreich Ataxia (FA) is difficult to quantify. This study evaluated a series of performance measures for speech in 22 patients with genetically confirmed FA and 16 ageβmatched controls. Tests included the PATA examination, the PATAKA examination, the Oral Motor component
## Abstract Cardiomyopathy is an important and frequently life limiting manifestation of Friedreich's ataxia (FA), the most prevalent form of autosomal recessive ataxia. Left ventricular mass is used as primary outcome measure in recent intervention studies but systematic analyses of FA cardiomyopa