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.

Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look‐alike?

Identifieur interne : 004527 ( Main/Exploration ); précédent : 004526; suivant : 004528

Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look‐alike?

Auteurs : Jason D. Warren [Royaume-Uni] ; Catherine J. Mummery [Royaume-Uni] ; Amir S. Al-Din [Royaume-Uni] ; Peter Brown [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni]

Source :

RBID : ISTEX:DBF49DE948326A4C2BE40E06AF42D905B89DC337

Descripteurs français

English descriptors

Abstract

A 57‐year‐old man with a 5‐year history of progressive left‐sided rigidity and apraxia had extensive bilateral calcification of basal ganglia, centrum semiovale, dentate nuclei, and cerebellar white matter on brain imaging. The case is an example of radiological Fahr's disease accompanying a clinical syndrome of corticobasal degeneration. Possible pathogenetic and nosological implications of this association are discussed. © 2002 Movement Disorder Society

Url:
DOI: 10.1002/mds.10122


Affiliations:


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


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look‐alike?</title>
<author>
<name sortKey="Warren, Jason D" sort="Warren, Jason D" uniqKey="Warren J" first="Jason D." last="Warren">Jason D. Warren</name>
</author>
<author>
<name sortKey="Mummery, Catherine J" sort="Mummery, Catherine J" uniqKey="Mummery C" first="Catherine J." last="Mummery">Catherine J. Mummery</name>
</author>
<author>
<name sortKey="Al In, Amir S" sort="Al In, Amir S" uniqKey="Al In A" first="Amir S." last="Al-Din">Amir S. Al-Din</name>
</author>
<author>
<name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
</author>
<author>
<name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:DBF49DE948326A4C2BE40E06AF42D905B89DC337</idno>
<date when="2002" year="2002">2002</date>
<idno type="doi">10.1002/mds.10122</idno>
<idno type="url">https://api.istex.fr/document/DBF49DE948326A4C2BE40E06AF42D905B89DC337/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003006</idno>
<idno type="wicri:Area/Istex/Curation">003006</idno>
<idno type="wicri:Area/Istex/Checkpoint">002E19</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Warren J:corticobasal:degeneration:syndrome</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:12112208</idno>
<idno type="wicri:Area/PubMed/Corpus">003A50</idno>
<idno type="wicri:Area/PubMed/Curation">003A50</idno>
<idno type="wicri:Area/PubMed/Checkpoint">003B49</idno>
<idno type="wicri:Area/Ncbi/Merge">000801</idno>
<idno type="wicri:Area/Ncbi/Curation">000801</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000801</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Warren J:corticobasal:degeneration:syndrome</idno>
<idno type="wicri:Area/Main/Merge">006533</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:02-0368569</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">002741</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000580</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">002817</idno>
<idno type="wicri:doubleKey">0885-3185:2002:Warren J:corticobasal:degeneration:syndrome</idno>
<idno type="wicri:Area/Main/Merge">006856</idno>
<idno type="wicri:Area/Main/Curation">004527</idno>
<idno type="wicri:Area/Main/Exploration">004527</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look‐alike?</title>
<author>
<name sortKey="Warren, Jason D" sort="Warren, Jason D" uniqKey="Warren J" first="Jason D." last="Warren">Jason D. Warren</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>The National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Mummery, Catherine J" sort="Mummery, Catherine J" uniqKey="Mummery C" first="Catherine J." last="Mummery">Catherine J. Mummery</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>The National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Al In, Amir S" sort="Al In, Amir S" uniqKey="Al In A" first="Amir S." last="Al-Din">Amir S. Al-Din</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Pinderfields General Hospital, Wakefield</wicri:regionArea>
<wicri:noRegion>Wakefield</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>The National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Neurophysiology, Institute of Neurology, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>The National Hospital for Neurology and Neurosurgery, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Neurogenetics Unit, Institute of Neurology, Queen Square, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>New York</pubPlace>
<date type="published" when="2002-05">2002-05</date>
<biblScope unit="vol">17</biblScope>
<biblScope unit="issue">3</biblScope>
<biblScope unit="page" from="563">563</biblScope>
<biblScope unit="page" to="567">567</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">DBF49DE948326A4C2BE40E06AF42D905B89DC337</idno>
<idno type="DOI">10.1002/mds.10122</idno>
<idno type="ArticleID">MDS10122</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Adult</term>
<term>Basal Ganglia Diseases (complications)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Basal Ganglia Diseases (radiography)</term>
<term>Basal ganglion</term>
<term>Calcification</term>
<term>Calcinosis (complications)</term>
<term>Calcinosis (radiography)</term>
<term>Case study</term>
<term>Cerebral cortex</term>
<term>Degeneration</term>
<term>Differential diagnostic</term>
<term>Fahr's disease</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurodegenerative Diseases (complications)</term>
<term>Neurodegenerative Diseases (pathology)</term>
<term>Neurodegenerative Diseases (radiography)</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Pathogenesis</term>
<term>Syndrome</term>
<term>Tomography, X-Ray Computed</term>
<term>corticobasal degeneration</term>
<term>intracranial calcification</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Basal Ganglia Diseases</term>
<term>Calcinosis</term>
<term>Neurodegenerative Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Basal Ganglia Diseases</term>
<term>Neurodegenerative Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="radiography" xml:lang="en">
<term>Basal Ganglia Diseases</term>
<term>Calcinosis</term>
<term>Neurodegenerative Diseases</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Syndrome</term>
<term>Tomography, X-Ray Computed</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Adulte</term>
<term>Calcification</term>
<term>Cortex cérébral</term>
<term>Diagnostic différentiel</term>
<term>Dégénérescence</term>
<term>Etude cas</term>
<term>Fahr maladie</term>
<term>Imagerie RMN</term>
<term>Mâle</term>
<term>Noyau gris central</term>
<term>Pathogénie</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Adulte</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A 57‐year‐old man with a 5‐year history of progressive left‐sided rigidity and apraxia had extensive bilateral calcification of basal ganglia, centrum semiovale, dentate nuclei, and cerebellar white matter on brain imaging. The case is an example of radiological Fahr's disease accompanying a clinical syndrome of corticobasal degeneration. Possible pathogenetic and nosological implications of this association are discussed. © 2002 Movement Disorder Society</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Royaume-Uni</li>
</country>
<region>
<li>Angleterre</li>
<li>Grand Londres</li>
</region>
<settlement>
<li>Londres</li>
</settlement>
</list>
<tree>
<country name="Royaume-Uni">
<region name="Angleterre">
<name sortKey="Warren, Jason D" sort="Warren, Jason D" uniqKey="Warren J" first="Jason D." last="Warren">Jason D. Warren</name>
</region>
<name sortKey="Al In, Amir S" sort="Al In, Amir S" uniqKey="Al In A" first="Amir S." last="Al-Din">Amir S. Al-Din</name>
<name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
<name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
<name sortKey="Mummery, Catherine J" sort="Mummery, Catherine J" uniqKey="Mummery C" first="Catherine J." last="Mummery">Catherine J. Mummery</name>
<name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
<name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004527 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 004527 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:DBF49DE948326A4C2BE40E06AF42D905B89DC337
   |texte=   Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look‐alike?
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024