MovDisordV3, Main, Exploration, bibRecord, 002413

Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK‐2

Identifieur interne : 002413 ( Main/Exploration ); précédent : 002412; suivant : 002414

Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK‐2

Auteurs : Marianna Amboni [Italie] ; Maria Teresa Pellecchia [Italie] ; Autilia Cozzolino [Italie] ; Marina Picillo [Italie] ; Carmine Vitale [Italie] ; Paolo Barone [Italie] ; Andrea Varrone [Italie] ; Barbara Garavaglia [Italie] ; Simona Gambelli [Italie] ; Antonio Federico [Italie]

Source :

Movement Disorders [ 0885-3185 ] ; 2009-01-30.

RBID : ISTEX:085B7D0855EBCFCDD0999D05E7274E2036AD4E87

English descriptors

KwdEn :
- Adult, Blepharoptosis (etiology), Carbon Radioisotopes (diagnostic use), Cerebellum (physiopathology), Child, Preschool, Corpus Striatum (radionuclide imaging), Heterozygote, Humans, Hypokinesia (etiology), Iodine Radioisotopes (diagnostic use), Male, Mitochondria, Muscle (metabolism), Mitochondria, Muscle (ultrastructure), Muscle Weakness (etiology), Mutation, Missense, Parkinsonian Disorders (complications), Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics), Parkinsonian Disorders (radionuclide imaging), Sequence Deletion, Spinocerebellar Degenerations (etiology), Tropanes (diagnostic use), Ubiquitin-Protein Ligases (deficiency), Ubiquitin-Protein Ligases (genetics).
MESH :
- chemical , deficiency : Ubiquitin-Protein Ligases.
- chemical , diagnostic use : Carbon Radioisotopes, Iodine Radioisotopes, Tropanes.
- complications : Parkinsonian Disorders.
- diagnosis : Parkinsonian Disorders.
- etiology : Blepharoptosis, Hypokinesia, Muscle Weakness, Spinocerebellar Degenerations.
- genetics : Parkinsonian Disorders, Ubiquitin-Protein Ligases.
- metabolism : Mitochondria, Muscle.
- physiopathology : Cerebellum.
- radionuclide imaging : Corpus Striatum, Parkinsonian Disorders.
- ultrastructure : Mitochondria, Muscle.
- Adult, Child, Preschool, Heterozygote, Humans, Male, Mutation, Missense, Sequence Deletion.

Url:

https://api.istex.fr/document/085B7D0855EBCFCDD0999D05E7274E2036AD4E87/fulltext/pdf

DOI: 10.1002/mds.22342

Affiliations:

Italie

Le document en format XML

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<author><name sortKey="Amboni, Marianna" sort="Amboni, Marianna" uniqKey="Amboni M" first="Marianna" last="Amboni">Marianna Amboni</name>
</author>
<author><name sortKey="Pellecchia, Maria Teresa" sort="Pellecchia, Maria Teresa" uniqKey="Pellecchia M" first="Maria Teresa" last="Pellecchia">Maria Teresa Pellecchia</name>
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<author><name sortKey="Cozzolino, Autilia" sort="Cozzolino, Autilia" uniqKey="Cozzolino A" first="Autilia" last="Cozzolino">Autilia Cozzolino</name>
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<author><name sortKey="Picillo, Marina" sort="Picillo, Marina" uniqKey="Picillo M" first="Marina" last="Picillo">Marina Picillo</name>
</author>
<author><name sortKey="Vitale, Carmine" sort="Vitale, Carmine" uniqKey="Vitale C" first="Carmine" last="Vitale">Carmine Vitale</name>
</author>
<author><name sortKey="Barone, Paolo" sort="Barone, Paolo" uniqKey="Barone P" first="Paolo" last="Barone">Paolo Barone</name>
</author>
<author><name sortKey="Varrone, Andrea" sort="Varrone, Andrea" uniqKey="Varrone A" first="Andrea" last="Varrone">Andrea Varrone</name>
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<author><name sortKey="Garavaglia, Barbara" sort="Garavaglia, Barbara" uniqKey="Garavaglia B" first="Barbara" last="Garavaglia">Barbara Garavaglia</name>
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<author><name sortKey="Gambelli, Simona" sort="Gambelli, Simona" uniqKey="Gambelli S" first="Simona" last="Gambelli">Simona Gambelli</name>
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<author><name sortKey="Federico, Antonio" sort="Federico, Antonio" uniqKey="Federico A" first="Antonio" last="Federico">Antonio Federico</name>
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<author><name sortKey="Pellecchia, Maria Teresa" sort="Pellecchia, Maria Teresa" uniqKey="Pellecchia M" first="Maria Teresa" last="Pellecchia">Maria Teresa Pellecchia</name>
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<author><name sortKey="Cozzolino, Autilia" sort="Cozzolino, Autilia" uniqKey="Cozzolino A" first="Autilia" last="Cozzolino">Autilia Cozzolino</name>
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<wicri:regionArea>Department of Neurological Sciences, University of Napoli “Federico II”</wicri:regionArea>
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<author><name sortKey="Picillo, Marina" sort="Picillo, Marina" uniqKey="Picillo M" first="Marina" last="Picillo">Marina Picillo</name>
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<author><name sortKey="Vitale, Carmine" sort="Vitale, Carmine" uniqKey="Vitale C" first="Carmine" last="Vitale">Carmine Vitale</name>
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<author><name sortKey="Barone, Paolo" sort="Barone, Paolo" uniqKey="Barone P" first="Paolo" last="Barone">Paolo Barone</name>
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<author><name sortKey="Garavaglia, Barbara" sort="Garavaglia, Barbara" uniqKey="Garavaglia B" first="Barbara" last="Garavaglia">Barbara Garavaglia</name>
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<author><name sortKey="Gambelli, Simona" sort="Gambelli, Simona" uniqKey="Gambelli S" first="Simona" last="Gambelli">Simona Gambelli</name>
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<author><name sortKey="Federico, Antonio" sort="Federico, Antonio" uniqKey="Federico A" first="Antonio" last="Federico">Antonio Federico</name>
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<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>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Blepharoptosis (etiology)</term>
<term>Carbon Radioisotopes (diagnostic use)</term>
<term>Cerebellum (physiopathology)</term>
<term>Child, Preschool</term>
<term>Corpus Striatum (radionuclide imaging)</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Hypokinesia (etiology)</term>
<term>Iodine Radioisotopes (diagnostic use)</term>
<term>Male</term>
<term>Mitochondria, Muscle (metabolism)</term>
<term>Mitochondria, Muscle (ultrastructure)</term>
<term>Muscle Weakness (etiology)</term>
<term>Mutation, Missense</term>
<term>Parkinsonian Disorders (complications)</term>
<term>Parkinsonian Disorders (diagnosis)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Parkinsonian Disorders (radionuclide imaging)</term>
<term>Sequence Deletion</term>
<term>Spinocerebellar Degenerations (etiology)</term>
<term>Tropanes (diagnostic use)</term>
<term>Ubiquitin-Protein Ligases (deficiency)</term>
<term>Ubiquitin-Protein Ligases (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="diagnostic use" xml:lang="en"><term>Carbon Radioisotopes</term>
<term>Iodine Radioisotopes</term>
<term>Tropanes</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Blepharoptosis</term>
<term>Hypokinesia</term>
<term>Muscle Weakness</term>
<term>Spinocerebellar Degenerations</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinsonian Disorders</term>
<term>Ubiquitin-Protein Ligases</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Mitochondria, Muscle</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Cerebellum</term>
</keywords>
<keywords scheme="MESH" qualifier="radionuclide imaging" xml:lang="en"><term>Corpus Striatum</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>Mitochondria, Muscle</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Child, Preschool</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation, Missense</term>
<term>Sequence Deletion</term>
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<affiliations><list><country><li>Italie</li>
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<tree><country name="Italie"><noRegion><name sortKey="Amboni, Marianna" sort="Amboni, Marianna" uniqKey="Amboni M" first="Marianna" last="Amboni">Marianna Amboni</name>
</noRegion>
<name sortKey="Amboni, Marianna" sort="Amboni, Marianna" uniqKey="Amboni M" first="Marianna" last="Amboni">Marianna Amboni</name>
<name sortKey="Barone, Paolo" sort="Barone, Paolo" uniqKey="Barone P" first="Paolo" last="Barone">Paolo Barone</name>
<name sortKey="Barone, Paolo" sort="Barone, Paolo" uniqKey="Barone P" first="Paolo" last="Barone">Paolo Barone</name>
<name sortKey="Cozzolino, Autilia" sort="Cozzolino, Autilia" uniqKey="Cozzolino A" first="Autilia" last="Cozzolino">Autilia Cozzolino</name>
<name sortKey="Cozzolino, Autilia" sort="Cozzolino, Autilia" uniqKey="Cozzolino A" first="Autilia" last="Cozzolino">Autilia Cozzolino</name>
<name sortKey="Federico, Antonio" sort="Federico, Antonio" uniqKey="Federico A" first="Antonio" last="Federico">Antonio Federico</name>
<name sortKey="Gambelli, Simona" sort="Gambelli, Simona" uniqKey="Gambelli S" first="Simona" last="Gambelli">Simona Gambelli</name>
<name sortKey="Garavaglia, Barbara" sort="Garavaglia, Barbara" uniqKey="Garavaglia B" first="Barbara" last="Garavaglia">Barbara Garavaglia</name>
<name sortKey="Pellecchia, Maria Teresa" sort="Pellecchia, Maria Teresa" uniqKey="Pellecchia M" first="Maria Teresa" last="Pellecchia">Maria Teresa Pellecchia</name>
<name sortKey="Pellecchia, Maria Teresa" sort="Pellecchia, Maria Teresa" uniqKey="Pellecchia M" first="Maria Teresa" last="Pellecchia">Maria Teresa Pellecchia</name>
<name sortKey="Picillo, Marina" sort="Picillo, Marina" uniqKey="Picillo M" first="Marina" last="Picillo">Marina Picillo</name>
<name sortKey="Picillo, Marina" sort="Picillo, Marina" uniqKey="Picillo M" first="Marina" last="Picillo">Marina Picillo</name>
<name sortKey="Varrone, Andrea" sort="Varrone, Andrea" uniqKey="Varrone A" first="Andrea" last="Varrone">Andrea Varrone</name>
<name sortKey="Vitale, Carmine" sort="Vitale, Carmine" uniqKey="Vitale C" first="Carmine" last="Vitale">Carmine Vitale</name>
<name sortKey="Vitale, Carmine" sort="Vitale, Carmine" uniqKey="Vitale C" first="Carmine" last="Vitale">Carmine Vitale</name>
</country>
</tree>
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Movement Disorders (revue)

Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK‐2

Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK‐2

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	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.