MovDisordV3, Main, Curation, bibRecord, 004456

Forty‐one year follow‐up of childhood‐onset opsoclonus‐myoclonus‐ataxia: Cerebellar atrophy, multiphasic relapses, and response to IVIG

Identifieur interne : 004456 ( Main/Curation ); précédent : 004455; suivant : 004457

Forty‐one year follow‐up of childhood‐onset opsoclonus‐myoclonus‐ataxia: Cerebellar atrophy, multiphasic relapses, and response to IVIG

Auteurs : Michael R. Pranzatelli [États-Unis] ; Elizabeth D. Tate [États-Unis] ; Marcel Kinsbourne [États-Unis] ; Verne S. Caviness Jr. [États-Unis] ; Bibhuti Mishra [États-Unis]

Source :

Movement Disorders [ 0885-3185 ] ; 2002-11.

RBID : ISTEX:2AFDE518A95D227143DDFE3C079A00475A22D4F0

Descripteurs français

Pascal (Inist)
- Adulte, Ataxie, Cervelet, Chimiothérapie, Etude cas, Evolution, Immunoglobuline, Myoclonie, Opsoclonie, Récidive, Voie intraveineuse.
Wicri :
- topic : Adulte.

English descriptors

KwdEn :
- ACTH, Adolescent, Adrenocorticotropic Hormone (therapeutic use), Adult, Ataxia, Atrophy, Case study, Cerebellar Ataxia (diagnosis), Cerebellar Ataxia (drug therapy), Cerebellum, Cerebellum (pathology), Chemotherapy, Child, Child, Preschool, Evolution, Follow-Up Studies, Humans, IVIG, Immunization, Passive, Immunoglobulins, Infant, Intravenous administration, Kinsbourne syndrome, Magnetic Resonance Imaging, Male, Myoclonus, Neurologic Examination, Neuropsychological Tests, Opsoclonus, Paraneoplastic Syndromes, Nervous System (diagnosis), Paraneoplastic Syndromes, Nervous System (drug therapy), Recurrence, Relapse, Treatment Outcome, cerebellar ataxia, dancing eyes, myoclonus.
MESH :
- chemical , therapeutic use : Adrenocorticotropic Hormone.
- diagnosis : Cerebellar Ataxia, Paraneoplastic Syndromes, Nervous System.
- drug therapy : Cerebellar Ataxia, Paraneoplastic Syndromes, Nervous System.
- pathology : Cerebellum.
- Adolescent, Adult, Atrophy, Child, Child, Preschool, Follow-Up Studies, Humans, Immunization, Passive, Infant, Magnetic Resonance Imaging, Male, Neurologic Examination, Neuropsychological Tests, Recurrence, Treatment Outcome.

Abstract

We report on an adult with opsoclonus‐myoclonus‐ataxia syndrome experiencing widely spaced neurological relapses, who was followed for 41 years. His responses to treatment are described. © 2002 Movement Disorder Society

Url:

https://api.istex.fr/document/2AFDE518A95D227143DDFE3C079A00475A22D4F0/fulltext/pdf

DOI: 10.1002/mds.10283

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Le document en format XML

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<front><div type="abstract" xml:lang="en">We report on an adult with opsoclonus-myoclonus-ataxia syndrome experiencing widely spaced neurological relapses, who was followed for 41 years. His responses to treatment are described.</div>
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<author><name sortKey="Mishra, Bibhuti" sort="Mishra, Bibhuti" uniqKey="Mishra B" first="Bibhuti" last="Mishra">Bibhuti Mishra</name>
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<idno type="doi">10.1002/mds.10283</idno>
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<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Forty‐one year follow‐up of childhood‐onset opsoclonus‐myoclonus‐ataxia: Cerebellar atrophy, multiphasic relapses, and response to IVIG</title>
<author><name sortKey="Pranzatelli, Michael R" sort="Pranzatelli, Michael R" uniqKey="Pranzatelli M" first="Michael R." last="Pranzatelli">Michael R. Pranzatelli</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>The National Pediatric Myoclonus Center, Departments of Neurology and Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois</wicri:regionArea>
<placeName><region type="state">Illinois</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Tate, Elizabeth D" sort="Tate, Elizabeth D" uniqKey="Tate E" first="Elizabeth D." last="Tate">Elizabeth D. Tate</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>The National Pediatric Myoclonus Center, Departments of Neurology and Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois</wicri:regionArea>
<placeName><region type="state">Illinois</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Kinsbourne, Marcel" sort="Kinsbourne, Marcel" uniqKey="Kinsbourne M" first="Marcel" last="Kinsbourne">Marcel Kinsbourne</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>New School University and Tufts University, Winchester, Massachusetts</wicri:regionArea>
<placeName><region type="state">Massachusetts</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Caviness Jr, Verne S" sort="Caviness Jr, Verne S" uniqKey="Caviness Jr V" first="Verne S." last="Caviness Jr.">Verne S. Caviness Jr.</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Massachusetts General Hospital, Boston, Massachusetts</wicri:regionArea>
<placeName><region type="state">Massachusetts</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Mishra, Bibhuti" sort="Mishra, Bibhuti" uniqKey="Mishra B" first="Bibhuti" last="Mishra">Bibhuti Mishra</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Temple University, Philadelphia, Pennsylvania</wicri:regionArea>
<placeName><region type="state">Pennsylvanie</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="2002-11">2002-11</date>
<biblScope unit="vol">17</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="1387">1387</biblScope>
<biblScope unit="page" to="1390">1390</biblScope>
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<idno type="ISSN">0885-3185</idno>
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<idno type="DOI">10.1002/mds.10283</idno>
<idno type="ArticleID">MDS10283</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>ACTH</term>
<term>Adolescent</term>
<term>Adrenocorticotropic Hormone (therapeutic use)</term>
<term>Adult</term>
<term>Atrophy</term>
<term>Cerebellar Ataxia (diagnosis)</term>
<term>Cerebellar Ataxia (drug therapy)</term>
<term>Cerebellum (pathology)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>IVIG</term>
<term>Immunization, Passive</term>
<term>Infant</term>
<term>Kinsbourne syndrome</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
<term>Neuropsychological Tests</term>
<term>Paraneoplastic Syndromes, Nervous System (diagnosis)</term>
<term>Paraneoplastic Syndromes, Nervous System (drug therapy)</term>
<term>Recurrence</term>
<term>Treatment Outcome</term>
<term>cerebellar ataxia</term>
<term>dancing eyes</term>
<term>myoclonus</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Adrenocorticotropic Hormone</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cerebellar Ataxia</term>
<term>Paraneoplastic Syndromes, Nervous System</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Cerebellar Ataxia</term>
<term>Paraneoplastic Syndromes, Nervous System</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cerebellum</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Atrophy</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Immunization, Passive</term>
<term>Infant</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
<term>Neuropsychological Tests</term>
<term>Recurrence</term>
<term>Treatment Outcome</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We report on an adult with opsoclonus‐myoclonus‐ataxia syndrome experiencing widely spaced neurological relapses, who was followed for 41 years. His responses to treatment are described. © 2002 Movement Disorder Society</div>
</front>
</TEI>
</ISTEX>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Forty‐one year follow‐up of childhood‐onset opsoclonus‐myoclonus‐ataxia: Cerebellar atrophy, multiphasic relapses, and response to IVIG

Forty‐one year follow‐up of childhood‐onset opsoclonus‐myoclonus‐ataxia: Cerebellar atrophy, multiphasic relapses, and response to IVIG

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