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Cranial magnetic resonance imaging in genetically proven myotonic dystrophy type 1 and 2

✍ Scribed by Cornelia Kornblum; Jürgen Reul; Wolfram Kress; Christoph Grothe; Niki Amanatidis; Thomas Klockgether; Rolf Schröder


Publisher
Springer
Year
2004
Tongue
English
Weight
281 KB
Volume
251
Category
Article
ISSN
0340-5354

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## Abstract The objective of this study was to investigate cerebellar metabolism in patients with autosomal dominant cerebellar ataxia type 1 (ADCA‐I) carrying two distinct mutations of spinocerebellar ataxia (SCA). Non‐invasive image‐guided proton magnetic resonance spectroscopy imaging (1H‐MRSI)