Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
Identifieur interne : 000941 ( Main/Exploration ); précédent : 000940; suivant : 000942Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
Auteurs : Jennifer Müller Vom Hagen [Allemagne] ; Matthis Synofzik ; Julia Schicks ; Ingeborg Kr Geloh-Mann ; Ludger SchölsSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Adolescent, Adult, Aged, Ataxia (complications), Cognition Disorders (etiology), Female, Hereditary Central Nervous System Demyelinating Diseases (complications), Hereditary Central Nervous System Demyelinating Diseases (pathology), Humans, Magnetic Resonance Imaging, Male, Middle Aged, Nerve Fibers, Myelinated (pathology), Phenotype, Young Adult.
- MESH :
- complications : Ataxia, Hereditary Central Nervous System Demyelinating Diseases.
- etiology : Cognition Disorders.
- pathology : Hereditary Central Nervous System Demyelinating Diseases, Nerve Fibers, Myelinated.
- Adolescent, Adult, Aged, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Phenotype, Young Adult.
DOI: 10.1002/mds.25617
PubMed: 23926051
Affiliations:
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Le document en format XML
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