MovDisordV3, Ncbi, Merge, bibRecord, 003D09

Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.

Identifieur interne : 003D09 ( Ncbi/Merge ); précédent : 003D08; suivant : 003D10

Leukodystrophies 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 Schöls

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:23926051

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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to stream PubMed, to step Checkpoint: 000955

Links to Exploration step

pubmed:23926051

Le document en format XML

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<author><name sortKey="Muller Vom Hagen, Jennifer" sort="Muller Vom Hagen, Jennifer" uniqKey="Muller Vom Hagen J" first="Jennifer" last="Müller Vom Hagen">Jennifer Müller Vom Hagen</name>
<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>
<placeName><region type="land" nuts="1">Bade-Wurtemberg</region>
<region type="district" nuts="2">District de Tübingen</region>
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<author><name sortKey="Synofzik, Matthis" sort="Synofzik, Matthis" uniqKey="Synofzik M" first="Matthis" last="Synofzik">Matthis Synofzik</name>
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<author><name sortKey="Schicks, Julia" sort="Schicks, Julia" uniqKey="Schicks J" first="Julia" last="Schicks">Julia Schicks</name>
</author>
<author><name sortKey="Kr Geloh Mann, Ingeborg" sort="Kr Geloh Mann, Ingeborg" uniqKey="Kr Geloh Mann I" first="Ingeborg" last="Kr Geloh-Mann">Ingeborg Kr Geloh-Mann</name>
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<author><name sortKey="Schols, Ludger" sort="Schols, Ludger" uniqKey="Schols L" first="Ludger" last="Schöls">Ludger Schöls</name>
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<author><name sortKey="Kr Geloh Mann, Ingeborg" sort="Kr Geloh Mann, Ingeborg" uniqKey="Kr Geloh Mann I" first="Ingeborg" last="Kr Geloh-Mann">Ingeborg Kr Geloh-Mann</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Adult</term>
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<term>Cognition Disorders (etiology)</term>
<term>Female</term>
<term>Hereditary Central Nervous System Demyelinating Diseases (complications)</term>
<term>Hereditary Central Nervous System Demyelinating Diseases (pathology)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Nerve Fibers, Myelinated (pathology)</term>
<term>Phenotype</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Ataxia</term>
<term>Hereditary Central Nervous System Demyelinating Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Cognition Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hereditary Central Nervous System Demyelinating Diseases</term>
<term>Nerve Fibers, Myelinated</term>
</keywords>
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<term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
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<Month>12</Month>
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<DateCompleted><Year>2014</Year>
<Month>07</Month>
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<Issue>14</Issue>
<PubDate><Year>2013</Year>
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</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.</ArticleTitle>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Müller Vom Hagen</LastName>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.

Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki