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Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.

par Reetz, Kathrin;Costa, Ana Sofia;Mirzazade, Shahram;Lehmann, Anna;Juzek, Agnes;Rakowicz, Maria;Boguslawska, Romana;Schöls, Lüdger;Linnemann, Christoph;Mariotti, Caterina;Grisoli, Marina;Dürr, Alexandra;van de Warrenburg, Bart P;Timmann, Dagmar;Pandolfo, Massimo ;Bauer, Peter;Jacobi, Heike;Hauser, Till-Karsten;Klockgether, Thomas;Schulz, Jörg Bernhard;axia Study Group Investigators,
Référence Brain, 136, Pt 3, page (905-917)
Publication Publié, 2013-03

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Titre:	Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Auteur:	Reetz, Kathrin; Costa, Ana Sofia; Mirzazade, Shahram; Lehmann, Anna; Juzek, Agnes; Rakowicz, Maria; Boguslawska, Romana; Schöls, Lüdger; Linnemann, Christoph; Mariotti, Caterina; Grisoli, Marina; Dürr, Alexandra; van de Warrenburg, Bart P; Timmann, Dagmar; Pandolfo, Massimo; Bauer, Peter; Jacobi, Heike; Hauser, Till-Karsten; Klockgether, Thomas; Schulz, Jörg Bernhard; axia Study Group Investigators,
Informations sur la publication:	Brain, 136, Pt 3, page (905-917)
Statut de publication:	Publié, 2013-03
Sujet CREF:	Neurologie
MeSH keywords:	Adult
	Atrophy -- pathology
	Brain -- pathology
	Disease Progression
	Female
	Genotype
	Humans
	Magnetic Resonance Imaging
	Male
	Middle Aged
	Spinocerebellar Ataxias -- complications -- genetics -- pathology
Note générale:	Journal Article
	Research Support, Non-U.S. Gov't
	SCOPUS: ar.j
Langue:	Anglais
Identificateurs:	urn:issn:0006-8950
	info:doi/10.1093/brain/aws369
	info:pii/aws369
	info:scp/84874913811
	info:pmid/23423669