Movement Disorders (revue)

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Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.

Identifieur interne : 002105 ( Ncbi/Merge ); précédent : 002104; suivant : 002106

Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.

Auteurs : Hélio A G. Teive ; Renato P. Munhoz ; Juliano A. Muzzio ; Rosana H. Scola ; Cláudia K. Kay ; Salmo Raskin ; Lineu C. Werneck ; Helene Bruhn

Source :

RBID : pubmed:18412280

English descriptors


DOI: 10.1002/mds.21990
PubMed: 18412280

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pubmed:18412280

Le document en format XML

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<title xml:lang="en">Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.</title>
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<name sortKey="Teive, Helio A G" sort="Teive, Helio A G" uniqKey="Teive H" first="Hélio A G" last="Teive">Hélio A G. Teive</name>
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<name sortKey="Munhoz, Renato P" sort="Munhoz, Renato P" uniqKey="Munhoz R" first="Renato P" last="Munhoz">Renato P. Munhoz</name>
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<name sortKey="Muzzio, Juliano A" sort="Muzzio, Juliano A" uniqKey="Muzzio J" first="Juliano A" last="Muzzio">Juliano A. Muzzio</name>
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<name sortKey="Scola, Rosana H" sort="Scola, Rosana H" uniqKey="Scola R" first="Rosana H" last="Scola">Rosana H. Scola</name>
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<name sortKey="Raskin, Salmo" sort="Raskin, Salmo" uniqKey="Raskin S" first="Salmo" last="Raskin">Salmo Raskin</name>
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<name sortKey="Werneck, Lineu C" sort="Werneck, Lineu C" uniqKey="Werneck L" first="Lineu C" last="Werneck">Lineu C. Werneck</name>
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<term>Alleles</term>
<term>Atrophy</term>
<term>Biopsy</term>
<term>Cerebellar Ataxia (diagnosis)</term>
<term>Cerebellar Ataxia (genetics)</term>
<term>Cerebellum (pathology)</term>
<term>DNA, Mitochondrial (genetics)</term>
<term>Dysarthria (diagnosis)</term>
<term>Dysarthria (genetics)</term>
<term>Head and Neck Neoplasms (diagnosis)</term>
<term>Head and Neck Neoplasms (genetics)</term>
<term>Humans</term>
<term>Lipoma (diagnosis)</term>
<term>Lipoma (genetics)</term>
<term>MERRF Syndrome (diagnosis)</term>
<term>MERRF Syndrome (genetics)</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Muscle, Skeletal (pathology)</term>
<term>Myoclonus (diagnosis)</term>
<term>Myoclonus (genetics)</term>
<term>Neurologic Examination</term>
<term>Point Mutation</term>
<term>RNA, Transfer, Lys (genetics)</term>
<term>Tomography, X-Ray Computed</term>
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<term>DNA, Mitochondrial</term>
<term>RNA, Transfer, Lys</term>
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<term>Cerebellar Ataxia</term>
<term>Dysarthria</term>
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<term>Lipoma</term>
<term>MERRF Syndrome</term>
<term>Myoclonus</term>
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<term>Cerebellar Ataxia</term>
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<term>Lipoma</term>
<term>MERRF Syndrome</term>
<term>Myoclonus</term>
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<term>Muscle, Skeletal</term>
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<term>Alleles</term>
<term>Atrophy</term>
<term>Biopsy</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
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<name sortKey="Munhoz, Renato P" sort="Munhoz, Renato P" uniqKey="Munhoz R" first="Renato P" last="Munhoz">Renato P. Munhoz</name>
<name sortKey="Muzzio, Juliano A" sort="Muzzio, Juliano A" uniqKey="Muzzio J" first="Juliano A" last="Muzzio">Juliano A. Muzzio</name>
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