Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
Identifieur interne : 003D09 ( Ncbi/Curation ); précédent : 003D08; suivant : 003D10Leukodystrophies 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
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pubmed:23926051Le document en format XML
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<affiliation wicri:level="3"><nlm:affiliation>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen</wicri:regionArea>
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