MovDisordV3, Main, Curation, bibRecord, 006276

Rett syndrome and associated movement disorders

Identifieur interne : 006276 ( Main/Curation ); précédent : 006275; suivant : 006277

Rett syndrome and associated movement disorders

Auteurs : Patricia M. Fitzgerald [États-Unis] ; Jankovic [États-Unis] ; Alan K. Percy [États-Unis]

Source :

Movement Disorders [ 0885-3185 ] ; 1990.

RBID : ISTEX:0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9

Descripteurs français

Pascal (Inist)
- Age, Diagnostic, Enfant, Etude cas, Exploration clinique, Extrapyramidal syndrome, Maladie dégénérative, Mouvement involontaire, Retard psychomoteur, Rett syndrome, Système nerveux pathologie, Trouble comportement, Trouble moteur.
Wicri :
- topic : Enfant.

English descriptors

KwdEn :
- Adolescent, Adult, Age, Behavioral disorder, Bruxism, Case study, Child, Child, Preschool, Chorea, Clinical investigation, Degenerative disease, Diagnosis, Dystonia, Extrapyramidal syndrome, Female, Gait disturbance, Humans, Infant, Involuntary movement, Motor system disorder, Movement Disorders (etiology), Movement Disorders (physiopathology), Myoclonus, Nervous system diseases, Oculogyric crisis, Parkinsonism, Psychomotor retardation, Rett Syndrome (complications), Rett Syndrome (physiopathology), Rett syndrome, Stereotyped Behavior, Stereotypies.
MESH :
- complications : Rett Syndrome.
- etiology : Movement Disorders.
- physiopathology : Movement Disorders, Rett Syndrome.
- Adolescent, Adult, Child, Child, Preschool, Female, Humans, Infant, Stereotyped Behavior.

Abstract

Rett syndrome, a progressive neurodegenerative disorder described only in female subjects, is manifested by a wide spectrum of behavioral and motor abnormalities. We studied 32 patients with this disorder, ages 30 months to 28 years old, and characterized their extrapyramidal disturbance. The most common motor abnormalities were stereotyped movements and gait disturbance, seen in all patients. Bruxism, oculogyric crises, parkinsonism, and dystonia were also common, but myoclonus and choreoathetosis were seen only infrequently. The hyperkinetic movement disorders tended to dominate in younger patients, while bradykinetic disorders were more evident in the older patients. This study provides evidence that movement disorders seen in Rett syndrome reflect age‐related neurodegenerative changes in the basal ganglia.

Url:

https://api.istex.fr/document/0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9/fulltext/pdf

DOI: 10.1002/mds.870050303

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

to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :002099
to stream Istex, to step Curation: Pour aller vers cette notice dans l'étape Curation :002099
to stream Istex, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004365
to stream PubMed, to step Corpus: Pour aller vers cette notice dans l'étape Curation :004E73
to stream PubMed, to step Curation: Pour aller vers cette notice dans l'étape Curation :004E73
to stream PubMed, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004E78
to stream Ncbi, to step Merge: Pour aller vers cette notice dans l'étape Curation :003C67
to stream Ncbi, to step Curation: Pour aller vers cette notice dans l'étape Curation :003C67
to stream Ncbi, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :003C67
to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :009610
to stream PascalFrancis, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003931
to stream PascalFrancis, to step Curation: Pour aller vers cette notice dans l'étape Curation :002E94
to stream PascalFrancis, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :003925
to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :009701

Links to Exploration step

ISTEX:0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9

Le document en format XML

<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, Patricia M" sort="Fitzgerald, Patricia M" uniqKey="Fitzgerald P" first="Patricia M." last="Fitzgerald">Patricia M. Fitzgerald</name>
</author>
<author><name sortKey="Jankovic" sort="Jankovic" uniqKey="Jankovic" last="Jankovic">Jankovic</name>
</author>
<author><name sortKey="Percy, Alan K" sort="Percy, Alan K" uniqKey="Percy A" first="Alan K." last="Percy">Alan K. Percy</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9</idno>
<date when="1990" year="1990">1990</date>
<idno type="doi">10.1002/mds.870050303</idno>
<idno type="url">https://api.istex.fr/document/0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002099</idno>
<idno type="wicri:Area/Istex/Curation">002099</idno>
<idno type="wicri:Area/Istex/Checkpoint">004365</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:2388636</idno>
<idno type="wicri:Area/PubMed/Corpus">004E73</idno>
<idno type="wicri:Area/PubMed/Curation">004E73</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004E78</idno>
<idno type="wicri:Area/Ncbi/Merge">003C67</idno>
<idno type="wicri:Area/Ncbi/Curation">003C67</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">003C67</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:Area/Main/Merge">009610</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:91-0247269</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003931</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002E94</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003925</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:Area/Main/Merge">009701</idno>
<idno type="wicri:Area/Main/Curation">006276</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, Patricia M" sort="Fitzgerald, Patricia M" uniqKey="Fitzgerald P" first="Patricia M." last="Fitzgerald">Patricia M. Fitzgerald</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Baylor College of Medicine Department of Neurology, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jankovic" sort="Jankovic" uniqKey="Jankovic" last="Jankovic">Jankovic</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Baylor College of Medicine Department of Neurology, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Percy, Alan K" sort="Percy, Alan K" uniqKey="Percy A" first="Alan K." last="Percy">Alan K. Percy</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pediatrics, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</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>Hoboken</pubPlace>
<date type="published" when="1990">1990</date>
<biblScope unit="vol">5</biblScope>
<biblScope unit="issue">3</biblScope>
<biblScope unit="page" from="195">195</biblScope>
<biblScope unit="page" to="202">202</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9</idno>
<idno type="DOI">10.1002/mds.870050303</idno>
<idno type="ArticleID">MDS870050303</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age</term>
<term>Behavioral disorder</term>
<term>Bruxism</term>
<term>Case study</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Chorea</term>
<term>Clinical investigation</term>
<term>Degenerative disease</term>
<term>Diagnosis</term>
<term>Dystonia</term>
<term>Extrapyramidal syndrome</term>
<term>Female</term>
<term>Gait disturbance</term>
<term>Humans</term>
<term>Infant</term>
<term>Involuntary movement</term>
<term>Motor system disorder</term>
<term>Movement Disorders (etiology)</term>
<term>Movement Disorders (physiopathology)</term>
<term>Myoclonus</term>
<term>Nervous system diseases</term>
<term>Oculogyric crisis</term>
<term>Parkinsonism</term>
<term>Psychomotor retardation</term>
<term>Rett Syndrome (complications)</term>
<term>Rett Syndrome (physiopathology)</term>
<term>Rett syndrome</term>
<term>Stereotyped Behavior</term>
<term>Stereotypies</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Rett Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Movement Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Movement Disorders</term>
<term>Rett Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Stereotyped Behavior</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Age</term>
<term>Diagnostic</term>
<term>Enfant</term>
<term>Etude cas</term>
<term>Exploration clinique</term>
<term>Extrapyramidal syndrome</term>
<term>Maladie dégénérative</term>
<term>Mouvement involontaire</term>
<term>Retard psychomoteur</term>
<term>Rett syndrome</term>
<term>Système nerveux pathologie</term>
<term>Trouble comportement</term>
<term>Trouble moteur</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Enfant</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Rett syndrome, a progressive neurodegenerative disorder described only in female subjects, is manifested by a wide spectrum of behavioral and motor abnormalities. We studied 32 patients with this disorder, ages 30 months to 28 years old, and characterized their extrapyramidal disturbance. The most common motor abnormalities were stereotyped movements and gait disturbance, seen in all patients. Bruxism, oculogyric crises, parkinsonism, and dystonia were also common, but myoclonus and choreoathetosis were seen only infrequently. The hyperkinetic movement disorders tended to dominate in younger patients, while bradykinetic disorders were more evident in the older patients. This study provides evidence that movement disorders seen in Rett syndrome reflect age‐related neurodegenerative changes in the basal ganglia.</div>
</front>
</TEI>
<double idat="0885-3185:1990:Fitzgerald P:rett:syndrome:and"><INIST><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, P M" sort="Fitzgerald, P M" uniqKey="Fitzgerald P" first="P. M." last="Fitzgerald">P. M. Fitzgerald</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J." last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
<placeName><settlement type="city">Houston</settlement>
<region type="state">Texas</region>
</placeName>
<orgName type="university" n="3">Baylor College of Medicine</orgName>
</affiliation>
</author>
<author><name sortKey="Percy, A K" sort="Percy, A K" uniqKey="Percy A" first="A. K." last="Percy">A. K. Percy</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">91-0247269</idno>
<date when="1990">1990</date>
<idno type="stanalyst">PASCAL 91-0247269 INIST</idno>
<idno type="RBID">Pascal:91-0247269</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003931</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002E94</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003925</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:Area/Main/Merge">009701</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, P M" sort="Fitzgerald, P M" uniqKey="Fitzgerald P" first="P. M." last="Fitzgerald">P. M. Fitzgerald</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J." last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
<placeName><settlement type="city">Houston</settlement>
<region type="state">Texas</region>
</placeName>
<orgName type="university" n="3">Baylor College of Medicine</orgName>
</affiliation>
</author>
<author><name sortKey="Percy, A K" sort="Percy, A K" uniqKey="Percy A" first="A. K." last="Percy">A. K. Percy</name>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1990">1990</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Age</term>
<term>Behavioral disorder</term>
<term>Case study</term>
<term>Child</term>
<term>Clinical investigation</term>
<term>Degenerative disease</term>
<term>Diagnosis</term>
<term>Extrapyramidal syndrome</term>
<term>Involuntary movement</term>
<term>Motor system disorder</term>
<term>Nervous system diseases</term>
<term>Psychomotor retardation</term>
<term>Rett syndrome</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Mouvement involontaire</term>
<term>Trouble moteur</term>
<term>Extrapyramidal syndrome</term>
<term>Trouble comportement</term>
<term>Rett syndrome</term>
<term>Retard psychomoteur</term>
<term>Maladie dégénérative</term>
<term>Système nerveux pathologie</term>
<term>Diagnostic</term>
<term>Enfant</term>
<term>Age</term>
<term>Etude cas</term>
<term>Exploration clinique</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Enfant</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Rett syndrome, a progressive neurodegenerative disorder described only in female subjects, is manifested by a wide spectrum of behavioral and motor abnormalities. We studied 32 patients with this disorder, ages 30 months to 28 years old, and characterized their extrapyramidal disturbance</div>
</front>
</TEI>
</INIST>
<ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, Patricia M" sort="Fitzgerald, Patricia M" uniqKey="Fitzgerald P" first="Patricia M." last="Fitzgerald">Patricia M. Fitzgerald</name>
</author>
<author><name sortKey="Jankovic" sort="Jankovic" uniqKey="Jankovic" last="Jankovic">Jankovic</name>
</author>
<author><name sortKey="Percy, Alan K" sort="Percy, Alan K" uniqKey="Percy A" first="Alan K." last="Percy">Alan K. Percy</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9</idno>
<date when="1990" year="1990">1990</date>
<idno type="doi">10.1002/mds.870050303</idno>
<idno type="url">https://api.istex.fr/document/0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002099</idno>
<idno type="wicri:Area/Istex/Curation">002099</idno>
<idno type="wicri:Area/Istex/Checkpoint">004365</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:2388636</idno>
<idno type="wicri:Area/PubMed/Corpus">004E73</idno>
<idno type="wicri:Area/PubMed/Curation">004E73</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004E78</idno>
<idno type="wicri:Area/Ncbi/Merge">003C67</idno>
<idno type="wicri:Area/Ncbi/Curation">003C67</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">003C67</idno>
<idno type="wicri:doubleKey">0885-3185:1990:Fitzgerald P:rett:syndrome:and</idno>
<idno type="wicri:Area/Main/Merge">009610</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Rett syndrome and associated movement disorders</title>
<author><name sortKey="Fitzgerald, Patricia M" sort="Fitzgerald, Patricia M" uniqKey="Fitzgerald P" first="Patricia M." last="Fitzgerald">Patricia M. Fitzgerald</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Baylor College of Medicine Department of Neurology, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jankovic" sort="Jankovic" uniqKey="Jankovic" last="Jankovic">Jankovic</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Baylor College of Medicine Department of Neurology, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Percy, Alan K" sort="Percy, Alan K" uniqKey="Percy A" first="Alan K." last="Percy">Alan K. Percy</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pediatrics, Houston, Texas</wicri:regionArea>
<placeName><region type="state">Texas</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>Hoboken</pubPlace>
<date type="published" when="1990">1990</date>
<biblScope unit="vol">5</biblScope>
<biblScope unit="issue">3</biblScope>
<biblScope unit="page" from="195">195</biblScope>
<biblScope unit="page" to="202">202</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9</idno>
<idno type="DOI">10.1002/mds.870050303</idno>
<idno type="ArticleID">MDS870050303</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Bruxism</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Chorea</term>
<term>Dystonia</term>
<term>Female</term>
<term>Gait disturbance</term>
<term>Humans</term>
<term>Infant</term>
<term>Movement Disorders (etiology)</term>
<term>Movement Disorders (physiopathology)</term>
<term>Myoclonus</term>
<term>Oculogyric crisis</term>
<term>Parkinsonism</term>
<term>Rett Syndrome (complications)</term>
<term>Rett Syndrome (physiopathology)</term>
<term>Rett syndrome</term>
<term>Stereotyped Behavior</term>
<term>Stereotypies</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Rett Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Movement Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Movement Disorders</term>
<term>Rett Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Stereotyped Behavior</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Rett syndrome, a progressive neurodegenerative disorder described only in female subjects, is manifested by a wide spectrum of behavioral and motor abnormalities. We studied 32 patients with this disorder, ages 30 months to 28 years old, and characterized their extrapyramidal disturbance. The most common motor abnormalities were stereotyped movements and gait disturbance, seen in all patients. Bruxism, oculogyric crises, parkinsonism, and dystonia were also common, but myoclonus and choreoathetosis were seen only infrequently. The hyperkinetic movement disorders tended to dominate in younger patients, while bradykinetic disorders were more evident in the older patients. This study provides evidence that movement disorders seen in Rett syndrome reflect age‐related neurodegenerative changes in the basal ganglia.</div>
</front>
</TEI>
</ISTEX>
</double>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Curation

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 006276 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 006276 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Curation
   |type=    RBID
   |clé=     ISTEX:0543E5C43B9E3B4B8134B9F22FDECA0089EFBCA9
   |texte=   Rett syndrome and associated movement disorders
}}

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

	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.

Movement Disorders (revue)

Rett syndrome and associated movement disorders

Rett syndrome and associated movement disorders

Source :

Descripteurs français

English descriptors

Abstract

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

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri