Update on dopa-responsive dystonia: locus heterogeneity and biochemical features.
Identifieur interne : 000354 ( Ncbi/Curation ); précédent : 000353; suivant : 000355Update on dopa-responsive dystonia: locus heterogeneity and biochemical features.
Auteurs : Yoshiaki Furukawa [Canada]Source :
- Advances in neurology [ 0091-3952 ] ; 2004.
English descriptors
- KwdEn :
- Antiparkinson Agents (therapeutic use), Brain Chemistry, Dystonia (classification), Dystonia (complications), Dystonia (drug therapy), Dystonia (genetics), Family Health, GTP Cyclohydrolase (deficiency), GTP Cyclohydrolase (genetics), Genetic Heterogeneity, Genetic Linkage, Humans, Levodopa (therapeutic use), Motor Activity, Mutation, Parkinson Disease, Secondary (complications), Parkinson Disease, Secondary (genetics), Phenylketonurias (etiology), Phenylketonurias (genetics), Tyrosine 3-Monooxygenase (genetics).
- MESH :
- chemical , deficiency : GTP Cyclohydrolase.
- chemical , genetics : GTP Cyclohydrolase, Tyrosine 3-Monooxygenase.
- chemical , therapeutic use : Antiparkinson Agents, Levodopa.
- classification : Dystonia.
- complications : Dystonia, Parkinson Disease, Secondary.
- drug therapy : Dystonia.
- etiology : Phenylketonurias.
- genetics : Dystonia, Parkinson Disease, Secondary, Phenylketonurias.
- Brain Chemistry, Family Health, Genetic Heterogeneity, Genetic Linkage, Humans, Motor Activity, Mutation.
PubMed: 14509665
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pubmed:14509665Le document en format XML
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<affiliation wicri:level="1"><nlm:affiliation>Movement Disorders Research Laboratory, Centre for Addiction and Mental Health-Clarke Division, Toronto, Ontario, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
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<term>Dystonia (classification)</term>
<term>Dystonia (complications)</term>
<term>Dystonia (drug therapy)</term>
<term>Dystonia (genetics)</term>
<term>Family Health</term>
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<term>Motor Activity</term>
<term>Mutation</term>
<term>Parkinson Disease, Secondary (complications)</term>
<term>Parkinson Disease, Secondary (genetics)</term>
<term>Phenylketonurias (etiology)</term>
<term>Phenylketonurias (genetics)</term>
<term>Tyrosine 3-Monooxygenase (genetics)</term>
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<term>Tyrosine 3-Monooxygenase</term>
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<term>Parkinson Disease, Secondary</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Dystonia</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Phenylketonurias</term>
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<term>Parkinson Disease, Secondary</term>
<term>Phenylketonurias</term>
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<keywords scheme="MESH" xml:lang="en"><term>Brain Chemistry</term>
<term>Family Health</term>
<term>Genetic Heterogeneity</term>
<term>Genetic Linkage</term>
<term>Humans</term>
<term>Motor Activity</term>
<term>Mutation</term>
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