Report from a U.S. conference on essential tremor
Identifieur interne : 003207 ( Main/Exploration ); précédent : 003206; suivant : 003208Report from a U.S. conference on essential tremor
Auteurs : Rodger J. Elble [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2006-12.
Descripteurs français
- Wicri :
- geographic : États-Unis.
English descriptors
- KwdEn :
- MESH :
- geographic : United States.
- genetics : Essential Tremor.
- pathology : Essential Tremor.
- physiopathology : Essential Tremor.
- Congresses as Topic, Humans, International Cooperation.
Abstract
Seventy researchers met in Washington, DC, on 20–21 October 2005 to identify and discuss the most pressing research issues in essential tremor (ET). The conference attendees concluded that the following six objectives are of immediate and overriding importance: (1) a collaborative network of research centers; (2) an international committee for developing a standard protocol for the diagnosis and quantification of ET; (3) the identification of one or more genes for ET; (4) a centralized repository of DNA and, ideally, immortalized cell lines from well‐characterized ET families and healthy controls; (5) a reliable and efficient repository of optimally prepared and categorized brain samples for hypothesis‐driven neuropathological examinations in well‐characterized ET patients; and (6) animal models of ET for screening promising drugs. The conference attendees hope that this statement from the United States will engender international collaboration in finding a cure for ET. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.21157
Affiliations:
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Le document en format XML
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<term>clinical trials</term>
<term>essential tremor</term>
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<front><div type="abstract" xml:lang="fr">Seventy researchers met in Washington, DC, on 20–21 October 2005 to identify and discuss the most pressing research issues in essential tremor (ET). The conference attendees concluded that the following six objectives are of immediate and overriding importance: (1) a collaborative network of research centers; (2) an international committee for developing a standard protocol for the diagnosis and quantification of ET; (3) the identification of one or more genes for ET; (4) a centralized repository of DNA and, ideally, immortalized cell lines from well‐characterized ET families and healthy controls; (5) a reliable and efficient repository of optimally prepared and categorized brain samples for hypothesis‐driven neuropathological examinations in well‐characterized ET patients; and (6) animal models of ET for screening promising drugs. The conference attendees hope that this statement from the United States will engender international collaboration in finding a cure for ET. © 2006 Movement Disorder Society</div>
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