MovDisordV3, Main, Exploration, bibRecord, 001760

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG33 repeat length in the Huntington's disease gene

Identifieur interne : 001760 ( Main/Exploration ); précédent : 001759; suivant : 001761

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG33 repeat length in the Huntington's disease gene

Auteurs : Ferdinando Squitieri [Italie] ; Mouna Esmaeilzadeh [Suède] ; Andrea Ciarmiello [Italie] ; Joseph Jankovic [États-Unis]

Source :

Movement Disorders [ 0885-3185 ] ; 2011-04.

RBID : ISTEX:73410CFAE5ECD2CB9AD61DE55B55829C5C711C04

Descripteurs français

Pascal (Inist)
- Chorée de Huntington, Glucose, Homme, Pathologie du système nerveux.
Wicri :
- topic : Glucose, Homme.

English descriptors

KwdEn :
- Aged, Caudate Nucleus (metabolism), Caudate Nucleus (radionuclide imaging), Fluorodeoxyglucose F18 (diagnostic use), Glucose, Glucose (metabolism), Human, Humans, Huntington Disease (genetics), Huntington Disease (pathology), Huntington Disease (radionuclide imaging), Huntington disease, Male, Nerve Tissue Proteins (genetics), Nervous system diseases, Nuclear Proteins (genetics), Positron-Emission Tomography (methods), Trinucleotide Repeats (genetics).
MESH :
- chemical , diagnostic use : Fluorodeoxyglucose F18.
- genetics : Huntington Disease, Nerve Tissue Proteins, Nuclear Proteins, Trinucleotide Repeats.
- metabolism : Caudate Nucleus, Glucose.
- methods : Positron-Emission Tomography.
- pathology : Huntington Disease.
- radionuclide imaging : Caudate Nucleus, Huntington Disease.
- Aged, Humans, Male.

Url:

https://api.istex.fr/document/73410CFAE5ECD2CB9AD61DE55B55829C5C711C04/fulltext/pdf

DOI: 10.1002/mds.23623

Affiliations:

Le document en format XML

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<author><name sortKey="Esmaeilzadeh, Mouna" sort="Esmaeilzadeh, Mouna" uniqKey="Esmaeilzadeh M" first="Mouna" last="Esmaeilzadeh">Mouna Esmaeilzadeh</name>
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<wicri:regionArea>Stockholm Brain Institute, Department of Clinical Neuroscience, Karolinska Institute, PET Centre, Karolinska University Hospital, Stockholm</wicri:regionArea>
<placeName><settlement type="city">Stockholm</settlement>
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<term>Fluorodeoxyglucose F18 (diagnostic use)</term>
<term>Glucose</term>
<term>Glucose (metabolism)</term>
<term>Human</term>
<term>Humans</term>
<term>Huntington Disease (genetics)</term>
<term>Huntington Disease (pathology)</term>
<term>Huntington Disease (radionuclide imaging)</term>
<term>Huntington disease</term>
<term>Male</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Nervous system diseases</term>
<term>Nuclear Proteins (genetics)</term>
<term>Positron-Emission Tomography (methods)</term>
<term>Trinucleotide Repeats (genetics)</term>
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<term>Nerve Tissue Proteins</term>
<term>Nuclear Proteins</term>
<term>Trinucleotide Repeats</term>
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<term>Glucose</term>
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<term>Huntington Disease</term>
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<term>Humans</term>
<term>Male</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Chorée de Huntington</term>
<term>Glucose</term>
<term>Homme</term>
<term>Pathologie du   système nerveux</term>
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Movement Disorders (revue)

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG33 repeat length in the Huntington's disease gene

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG33 repeat length in the Huntington's disease gene

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.