MovDisordV3, Main, Exploration, bibRecord, 001525

Myoclonus‐dystonia in 18p deletion syndrome

Identifieur interne : 001525 ( Main/Exploration ); précédent : 001524; suivant : 001526

Myoclonus‐dystonia in 18p deletion syndrome

Auteurs : Markus C. Kowarik [Allemagne] ; Sabine Langer [Allemagne] ; Corinna Keri [Allemagne] ; Bernhard Hemmer [Allemagne] ; Konrad Oexle [Allemagne] ; Juliane Winkelmann [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2011-02-15.

RBID : ISTEX:6DAC4B10E70D2E94C52E0791F66F76286F1D4656

Descripteurs français

Pascal (Inist)
- Dystonie, Délétion, Myoclonie, Pathologie du système nerveux.

English descriptors

KwdEn :
- Adult, Chromosome Deletion, Chromosome Disorders (complications), Chromosomes, Human, Pair 18, Deletion, Dystonia, Dystonia (etiology), Female, Humans, Karyotyping (methods), Magnetic Resonance Imaging (methods), Myoclonus, Myoclonus (etiology), Nervous system diseases.
MESH :
- complications : Chromosome Disorders.
- etiology : Dystonia, Myoclonus.
- methods : Karyotyping, Magnetic Resonance Imaging.
- Adult, Chromosome Deletion, Chromosomes, Human, Pair 18, Female, Humans.

Url:

https://api.istex.fr/document/6DAC4B10E70D2E94C52E0791F66F76286F1D4656/fulltext/pdf

DOI: 10.1002/mds.23446

Affiliations:

Le document en format XML

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<author><name sortKey="Langer, Sabine" sort="Langer, Sabine" uniqKey="Langer S" first="Sabine" last="Langer">Sabine Langer</name>
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<author><name sortKey="Keri, Corinna" sort="Keri, Corinna" uniqKey="Keri C" first="Corinna" last="Keri">Corinna Keri</name>
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<author><name sortKey="Hemmer, Bernhard" sort="Hemmer, Bernhard" uniqKey="Hemmer B" first="Bernhard" last="Hemmer">Bernhard Hemmer</name>
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<author><name sortKey="Oexle, Konrad" sort="Oexle, Konrad" uniqKey="Oexle K" first="Konrad" last="Oexle">Konrad Oexle</name>
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<author><name sortKey="Winkelmann, Juliane" sort="Winkelmann, Juliane" uniqKey="Winkelmann J" first="Juliane" last="Winkelmann">Juliane Winkelmann</name>
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<term>Dystonia</term>
<term>Dystonia (etiology)</term>
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Movement Disorders (revue)

Myoclonus‐dystonia in 18p deletion syndrome

Myoclonus‐dystonia in 18p deletion syndrome

Source :

Descripteurs français

English descriptors

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

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.