Movement Disorders (revue)

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Hyperhomocysteinaemia in treated patients with Huntington's disease homocysteine in HD

Identifieur interne : 003C95 ( Main/Exploration ); précédent : 003C94; suivant : 003C96

Hyperhomocysteinaemia in treated patients with Huntington's disease homocysteine in HD

Auteurs : Jürgen Andrich [Allemagne] ; Carsten Saft [Allemagne] ; Anneliese Arz [Allemagne] ; Birgit Schneider [Allemagne] ; Markus W. Agelink [Allemagne] ; Peter H. Kraus [Allemagne] ; Wilfried Kuhn [Allemagne] ; Thomas Müller [Allemagne]

Source :

RBID : ISTEX:4BAF0240DD74950C3471FB24A5DF43A7F144CB77

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English descriptors

Abstract

Significantly increased plasma total homocysteine levels (t‐Hcys) appeared in treated Huntington disease (HD) patients compared to controls and untreated HD subjects. Because the protein Huntingtin interacts with the homocysteine metabolism modulating enzyme cystathionine β‐synthase, we hypothesize that homocysteine promotes neurodegeneration in HD. © 2003 Movement Disorder Society

Url:
DOI: 10.1002/mds.10629


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Significantly increased plasma total homocysteine levels (t‐Hcys) appeared in treated Huntington disease (HD) patients compared to controls and untreated HD subjects. Because the protein Huntingtin interacts with the homocysteine metabolism modulating enzyme cystathionine β‐synthase, we hypothesize that homocysteine promotes neurodegeneration in HD. © 2003 Movement Disorder Society</div>
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