MovDisordV3, PubMed, Corpus, bibRecord, 002195

PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.

Identifieur interne : 002195 ( PubMed/Corpus ); précédent : 002194; suivant : 002196

PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.

Auteurs : Joong-Seok Kim ; Jae-Young An ; Kwang-Soo Lee ; Yong-An Chung ; Jin-Soo Choi ; Kwon-Haeng Lee

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.

RBID : pubmed:18546320

English descriptors

KwdEn :
- Adolescent, Adult, Age of Onset, Cerebellum (metabolism), Cerebellum (pathology), Cerebellum (radionuclide imaging), Dysarthria (genetics), Dysarthria (metabolism), Dysarthria (radionuclide imaging), Female, Fluorodeoxyglucose F18 (diagnostic use), Genes, Dominant, Humans, Kv1.1 Potassium Channel (genetics), Magnetic Resonance Imaging, Male, Middle Aged, Myokymia (genetics), Myokymia (metabolism), Myokymia (radionuclide imaging), Occipital Lobe (metabolism), Occipital Lobe (radionuclide imaging), Pedigree, Positron-Emission Tomography, Radioisotopes (diagnostic use), Spinocerebellar Degenerations (genetics), Spinocerebellar Degenerations (metabolism), Spinocerebellar Degenerations (radionuclide imaging), Syndrome.
MESH :
- chemical , diagnostic use : Fluorodeoxyglucose F18, Radioisotopes.
- genetics : Dysarthria, Kv1.1 Potassium Channel, Myokymia, Spinocerebellar Degenerations.
- metabolism : Cerebellum, Dysarthria, Myokymia, Occipital Lobe, Spinocerebellar Degenerations.
- pathology : Cerebellum.
- radionuclide imaging : Cerebellum, Dysarthria, Myokymia, Occipital Lobe, Spinocerebellar Degenerations.
- Adolescent, Adult, Age of Onset, Female, Genes, Dominant, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Pedigree, Positron-Emission Tomography, Syndrome.

DOI: 10.1002/mds.22154
PubMed: 18546320

Links to Exploration step

pubmed:18546320

Le document en format XML

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<author><name sortKey="Kim, Joong Seok" sort="Kim, Joong Seok" uniqKey="Kim J" first="Joong-Seok" last="Kim">Joong-Seok Kim</name>
</author>
<author><name sortKey="An, Jae Young" sort="An, Jae Young" uniqKey="An J" first="Jae-Young" last="An">Jae-Young An</name>
</author>
<author><name sortKey="Lee, Kwang Soo" sort="Lee, Kwang Soo" uniqKey="Lee K" first="Kwang-Soo" last="Lee">Kwang-Soo Lee</name>
</author>
<author><name sortKey="Chung, Yong An" sort="Chung, Yong An" uniqKey="Chung Y" first="Yong-An" last="Chung">Yong-An Chung</name>
</author>
<author><name sortKey="Choi, Jin Soo" sort="Choi, Jin Soo" uniqKey="Choi J" first="Jin-Soo" last="Choi">Jin-Soo Choi</name>
</author>
<author><name sortKey="Lee, Kwon Haeng" sort="Lee, Kwon Haeng" uniqKey="Lee K" first="Kwon-Haeng" last="Lee">Kwon-Haeng Lee</name>
</author>
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<date when="2008">2008</date>
<idno type="doi">10.1002/mds.22154</idno>
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<author><name sortKey="Kim, Joong Seok" sort="Kim, Joong Seok" uniqKey="Kim J" first="Joong-Seok" last="Kim">Joong-Seok Kim</name>
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<author><name sortKey="An, Jae Young" sort="An, Jae Young" uniqKey="An J" first="Jae-Young" last="An">Jae-Young An</name>
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<author><name sortKey="Lee, Kwang Soo" sort="Lee, Kwang Soo" uniqKey="Lee K" first="Kwang-Soo" last="Lee">Kwang-Soo Lee</name>
</author>
<author><name sortKey="Chung, Yong An" sort="Chung, Yong An" uniqKey="Chung Y" first="Yong-An" last="Chung">Yong-An Chung</name>
</author>
<author><name sortKey="Choi, Jin Soo" sort="Choi, Jin Soo" uniqKey="Choi J" first="Jin-Soo" last="Choi">Jin-Soo Choi</name>
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<author><name sortKey="Lee, Kwon Haeng" sort="Lee, Kwon Haeng" uniqKey="Lee K" first="Kwon-Haeng" last="Lee">Kwon-Haeng Lee</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Cerebellum (metabolism)</term>
<term>Cerebellum (pathology)</term>
<term>Cerebellum (radionuclide imaging)</term>
<term>Dysarthria (genetics)</term>
<term>Dysarthria (metabolism)</term>
<term>Dysarthria (radionuclide imaging)</term>
<term>Female</term>
<term>Fluorodeoxyglucose F18 (diagnostic use)</term>
<term>Genes, Dominant</term>
<term>Humans</term>
<term>Kv1.1 Potassium Channel (genetics)</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Myokymia (genetics)</term>
<term>Myokymia (metabolism)</term>
<term>Myokymia (radionuclide imaging)</term>
<term>Occipital Lobe (metabolism)</term>
<term>Occipital Lobe (radionuclide imaging)</term>
<term>Pedigree</term>
<term>Positron-Emission Tomography</term>
<term>Radioisotopes (diagnostic use)</term>
<term>Spinocerebellar Degenerations (genetics)</term>
<term>Spinocerebellar Degenerations (metabolism)</term>
<term>Spinocerebellar Degenerations (radionuclide imaging)</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="diagnostic use" xml:lang="en"><term>Fluorodeoxyglucose F18</term>
<term>Radioisotopes</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dysarthria</term>
<term>Kv1.1 Potassium Channel</term>
<term>Myokymia</term>
<term>Spinocerebellar Degenerations</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cerebellum</term>
<term>Dysarthria</term>
<term>Myokymia</term>
<term>Occipital Lobe</term>
<term>Spinocerebellar Degenerations</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cerebellum</term>
</keywords>
<keywords scheme="MESH" qualifier="radionuclide imaging" xml:lang="en"><term>Cerebellum</term>
<term>Dysarthria</term>
<term>Myokymia</term>
<term>Occipital Lobe</term>
<term>Spinocerebellar Degenerations</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Female</term>
<term>Genes, Dominant</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pedigree</term>
<term>Positron-Emission Tomography</term>
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<Day>05</Day>
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<DateCompleted><Year>2008</Year>
<Month>11</Month>
<Day>18</Day>
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<DateRevised><Year>2013</Year>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.</ArticleTitle>
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<Author ValidYN="Y"><LastName>Chung</LastName>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020385">Myokymia</DescriptorName>
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<QualifierName MajorTopicYN="Y" UI="Q000378">metabolism</QualifierName>
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</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009778">Occipital Lobe</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000378">metabolism</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000531">radionuclide imaging</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010375">Pedigree</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D049268">Positron-Emission Tomography</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013132">Spinocerebellar Degenerations</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000378">metabolism</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000531">radionuclide imaging</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013577">Syndrome</DescriptorName>
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	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)

PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.

PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.

Source :

English descriptors

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

Pour générer des pages wiki