PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.
Identifieur interne : 002195 ( PubMed/Corpus ); précédent : 002194; suivant : 002196PET 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 LeeSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.
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:18546320Le 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>
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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>
</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>
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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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<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>
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<author><name sortKey="Chung, Yong An" sort="Chung, Yong An" uniqKey="Chung Y" first="Yong-An" last="Chung">Yong-An Chung</name>
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<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>
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<keywords scheme="MESH" type="chemical" qualifier="diagnostic use" xml:lang="en"><term>Fluorodeoxyglucose F18</term>
<term>Radioisotopes</term>
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<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>
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<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>
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<Month>11</Month>
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<DateRevised><Year>2013</Year>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.</ArticleTitle>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020385">Myokymia</DescriptorName>
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<QualifierName MajorTopicYN="N" UI="Q000531">radionuclide imaging</QualifierName>
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