Cardiomyopathy in Friedreich's ataxia-assessment by cardiac MRI

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 cardiomyopathy are...

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Veröffentlicht in:	Movement disorders 2007-08, Vol.22 (11), p.1615-1622
Hauptverfasser:	Meyer, Chris, Schmid, Gebhard, Görlitz, Sabine, Ernst, Monika, Wilkens, Christian, Wilhelms, Inga, Kraus, Peter H., Bauer, Peter, Tomiuk, Jürgen, Przuntek, Horst, Mügge, Andreas, Schöls, Ludger
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Biological and medical sciences cardiac MRI Cardiomyopathies - etiology Cardiomyopathies - genetics Cardiomyopathies - pathology cardiomyopathy Case-Control Studies Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Echocardiography Female Friedreich Ataxia - complications Friedreich Ataxia - genetics Friedreich's ataxia Heart Septum - pathology Heart Ventricles - pathology Humans Investigative techniques, diagnostic techniques (general aspects) Longitudinal Studies Magnetic Resonance Imaging Medical sciences Middle Aged Myocardium - pathology Nervous system Neurology outcome measure for intervention trials Radiodiagnosis. Nmr imagery. Nmr spectrometry Trinucleotide Repeats - genetics
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