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.

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.

Identifieur interne : 003153 ( PubMed/Corpus ); précédent : 003152; suivant : 003154

Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.

Auteurs : Masahiko Suzuki ; Nobutaka Hattori ; Satoshi Orimo ; Nobuyoshi Fukumitsu ; Masahiro Abo ; Yu Kono ; Renpei Sengoku ; Akira Kurita ; Hidehiko Honda ; Kiyoharu Inoue

Source :

RBID : pubmed:15704207

English descriptors

Abstract

A decrease in myocardial uptake of iodine-123-labeled metaiodobenzylguanidine (123I-MIBG) has been reported in idiopathic Parkinson's disease (PD) using 123I-MIBG myocardial scintigraphy. However, the patient with autosomal recessive juvenile parkinsonism (AR-JP), caused by the parkin gene, presented here showed normal 123I-MIBG myocardial uptake, suggesting that AR-JP is a distinct disease entity from PD. Although the clinical features of AR-JP are sometimes quite similar to those of late-onset idiopathic PD, 123I-MIBG myocardial scintigraphy may be a powerful tool to differentiate PD from other parkinsonian syndromes, including AR-JP.

DOI: 10.1002/mds.20384
PubMed: 15704207

Links to Exploration step

pubmed:15704207

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.</title>
<author>
<name sortKey="Suzuki, Masahiko" sort="Suzuki, Masahiko" uniqKey="Suzuki M" first="Masahiko" last="Suzuki">Masahiko Suzuki</name>
<affiliation>
<nlm:affiliation>Department of Neurology, The Jikei University School of Medicine, Tokyo, Japan. suzukimd@jikei.ac.jp</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Hattori, Nobutaka" sort="Hattori, Nobutaka" uniqKey="Hattori N" first="Nobutaka" last="Hattori">Nobutaka Hattori</name>
</author>
<author>
<name sortKey="Orimo, Satoshi" sort="Orimo, Satoshi" uniqKey="Orimo S" first="Satoshi" last="Orimo">Satoshi Orimo</name>
</author>
<author>
<name sortKey="Fukumitsu, Nobuyoshi" sort="Fukumitsu, Nobuyoshi" uniqKey="Fukumitsu N" first="Nobuyoshi" last="Fukumitsu">Nobuyoshi Fukumitsu</name>
</author>
<author>
<name sortKey="Abo, Masahiro" sort="Abo, Masahiro" uniqKey="Abo M" first="Masahiro" last="Abo">Masahiro Abo</name>
</author>
<author>
<name sortKey="Kono, Yu" sort="Kono, Yu" uniqKey="Kono Y" first="Yu" last="Kono">Yu Kono</name>
</author>
<author>
<name sortKey="Sengoku, Renpei" sort="Sengoku, Renpei" uniqKey="Sengoku R" first="Renpei" last="Sengoku">Renpei Sengoku</name>
</author>
<author>
<name sortKey="Kurita, Akira" sort="Kurita, Akira" uniqKey="Kurita A" first="Akira" last="Kurita">Akira Kurita</name>
</author>
<author>
<name sortKey="Honda, Hidehiko" sort="Honda, Hidehiko" uniqKey="Honda H" first="Hidehiko" last="Honda">Hidehiko Honda</name>
</author>
<author>
<name sortKey="Inoue, Kiyoharu" sort="Inoue, Kiyoharu" uniqKey="Inoue K" first="Kiyoharu" last="Inoue">Kiyoharu Inoue</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2005">2005</date>
<idno type="doi">10.1002/mds.20384</idno>
<idno type="RBID">pubmed:15704207</idno>
<idno type="pmid">15704207</idno>
<idno type="wicri:Area/PubMed/Corpus">003153</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.</title>
<author>
<name sortKey="Suzuki, Masahiko" sort="Suzuki, Masahiko" uniqKey="Suzuki M" first="Masahiko" last="Suzuki">Masahiko Suzuki</name>
<affiliation>
<nlm:affiliation>Department of Neurology, The Jikei University School of Medicine, Tokyo, Japan. suzukimd@jikei.ac.jp</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Hattori, Nobutaka" sort="Hattori, Nobutaka" uniqKey="Hattori N" first="Nobutaka" last="Hattori">Nobutaka Hattori</name>
</author>
<author>
<name sortKey="Orimo, Satoshi" sort="Orimo, Satoshi" uniqKey="Orimo S" first="Satoshi" last="Orimo">Satoshi Orimo</name>
</author>
<author>
<name sortKey="Fukumitsu, Nobuyoshi" sort="Fukumitsu, Nobuyoshi" uniqKey="Fukumitsu N" first="Nobuyoshi" last="Fukumitsu">Nobuyoshi Fukumitsu</name>
</author>
<author>
<name sortKey="Abo, Masahiro" sort="Abo, Masahiro" uniqKey="Abo M" first="Masahiro" last="Abo">Masahiro Abo</name>
</author>
<author>
<name sortKey="Kono, Yu" sort="Kono, Yu" uniqKey="Kono Y" first="Yu" last="Kono">Yu Kono</name>
</author>
<author>
<name sortKey="Sengoku, Renpei" sort="Sengoku, Renpei" uniqKey="Sengoku R" first="Renpei" last="Sengoku">Renpei Sengoku</name>
</author>
<author>
<name sortKey="Kurita, Akira" sort="Kurita, Akira" uniqKey="Kurita A" first="Akira" last="Kurita">Akira Kurita</name>
</author>
<author>
<name sortKey="Honda, Hidehiko" sort="Honda, Hidehiko" uniqKey="Honda H" first="Hidehiko" last="Honda">Hidehiko Honda</name>
</author>
<author>
<name sortKey="Inoue, Kiyoharu" sort="Inoue, Kiyoharu" uniqKey="Inoue K" first="Kiyoharu" last="Inoue">Kiyoharu Inoue</name>
</author>
</analytic>
<series>
<title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2005" type="published">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>3-Iodobenzylguanidine (diagnostic use)</term>
<term>3-Iodobenzylguanidine (pharmacokinetics)</term>
<term>Exons (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Myocardium (metabolism)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Parkinsonian Disorders (radionuclide imaging)</term>
<term>Radionuclide Imaging</term>
<term>Radiopharmaceuticals (diagnostic use)</term>
<term>Radiopharmaceuticals (pharmacokinetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="diagnostic use" xml:lang="en">
<term>3-Iodobenzylguanidine</term>
<term>Radiopharmaceuticals</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en">
<term>3-Iodobenzylguanidine</term>
<term>Radiopharmaceuticals</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Exons</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Myocardium</term>
</keywords>
<keywords scheme="MESH" qualifier="radionuclide imaging" xml:lang="en">
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Radionuclide Imaging</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A decrease in myocardial uptake of iodine-123-labeled metaiodobenzylguanidine (123I-MIBG) has been reported in idiopathic Parkinson's disease (PD) using 123I-MIBG myocardial scintigraphy. However, the patient with autosomal recessive juvenile parkinsonism (AR-JP), caused by the parkin gene, presented here showed normal 123I-MIBG myocardial uptake, suggesting that AR-JP is a distinct disease entity from PD. Although the clinical features of AR-JP are sometimes quite similar to those of late-onset idiopathic PD, 123I-MIBG myocardial scintigraphy may be a powerful tool to differentiate PD from other parkinsonian syndromes, including AR-JP.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Owner="NLM" Status="MEDLINE">
<PMID Version="1">15704207</PMID>
<DateCreated>
<Year>2005</Year>
<Month>05</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted>
<Year>2005</Year>
<Month>09</Month>
<Day>01</Day>
</DateCompleted>
<DateRevised>
<Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>20</Volume>
<Issue>5</Issue>
<PubDate>
<Year>2005</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.</ArticleTitle>
<Pagination>
<MedlinePgn>634-6</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText>A decrease in myocardial uptake of iodine-123-labeled metaiodobenzylguanidine (123I-MIBG) has been reported in idiopathic Parkinson's disease (PD) using 123I-MIBG myocardial scintigraphy. However, the patient with autosomal recessive juvenile parkinsonism (AR-JP), caused by the parkin gene, presented here showed normal 123I-MIBG myocardial uptake, suggesting that AR-JP is a distinct disease entity from PD. Although the clinical features of AR-JP are sometimes quite similar to those of late-onset idiopathic PD, 123I-MIBG myocardial scintigraphy may be a powerful tool to differentiate PD from other parkinsonian syndromes, including AR-JP.</AbstractText>
<CopyrightInformation>Copyright 2005 Movement Disorder Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Suzuki</LastName>
<ForeName>Masahiko</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, The Jikei University School of Medicine, Tokyo, Japan. suzukimd@jikei.ac.jp</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hattori</LastName>
<ForeName>Nobutaka</ForeName>
<Initials>N</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Orimo</LastName>
<ForeName>Satoshi</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Fukumitsu</LastName>
<ForeName>Nobuyoshi</ForeName>
<Initials>N</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Abo</LastName>
<ForeName>Masahiro</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Kono</LastName>
<ForeName>Yu</ForeName>
<Initials>Y</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Sengoku</LastName>
<ForeName>Renpei</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Kurita</LastName>
<ForeName>Akira</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Honda</LastName>
<ForeName>Hidehiko</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Inoue</LastName>
<ForeName>Kiyoharu</ForeName>
<Initials>K</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D019275">Radiopharmaceuticals</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>35MRW7B4AD</RegistryNumber>
<NameOfSubstance UI="D019797">3-Iodobenzylguanidine</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D019797">3-Iodobenzylguanidine</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000176">diagnostic use</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000493">pharmacokinetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D005091">Exons</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D009206">Myocardium</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000378">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D020734">Parkinsonian Disorders</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000531">radionuclide imaging</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D011877">Radionuclide Imaging</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName MajorTopicYN="N" UI="D019275">Radiopharmaceuticals</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000176">diagnostic use</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000493">pharmacokinetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2005</Year>
<Month>2</Month>
<Day>11</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2005</Year>
<Month>9</Month>
<Day>2</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2005</Year>
<Month>2</Month>
<Day>11</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="doi">10.1002/mds.20384</ArticleId>
<ArticleId IdType="pubmed">15704207</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PubMed/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003153 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 003153 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    PubMed
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:15704207
   |texte=   Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i   -Sk "pubmed:15704207" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a MovDisordV3 

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