De novo FTL mutation: a clinical, neuroimaging, and molecular study.
Identifieur interne : 000A37 ( Main/Exploration ); précédent : 000A36; suivant : 000A38De novo FTL mutation: a clinical, neuroimaging, and molecular study.
Auteurs : Eugenia Storti ; Francesca Cortese ; Roberto Di Fabio ; Chiara Fiorillo ; Alberto Pierallini ; Alessandra Tessa ; Annamaria Valleriani ; Francesco Pierelli ; Filippo M. Santorelli ; Carlo CasaliSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Adult, Brain (pathology), Cholinergic Antagonists (therapeutic use), Dopamine Agonists (therapeutic use), Humans, Iron Metabolism Disorders (genetics), Iron Metabolism Disorders (pathology), Iron Metabolism Disorders (psychology), Magnetic Resonance Imaging, Male, Movement Disorders (genetics), Movement Disorders (pathology), Mutation (genetics), Neuroaxonal Dystrophies (genetics), Neuroaxonal Dystrophies (pathology), Neuroaxonal Dystrophies (psychology), Neuroimaging, Pyridones (therapeutic use), Treatment Failure, Tremor (etiology), Vascular Endothelial Growth Factor Receptor-1 (genetics).
- MESH :
- chemical , genetics : Vascular Endothelial Growth Factor Receptor-1.
- chemical , therapeutic use : Cholinergic Antagonists, Dopamine Agonists, Pyridones.
- etiology : Tremor.
- genetics : Iron Metabolism Disorders, Movement Disorders, Mutation, Neuroaxonal Dystrophies.
- pathology : Brain, Iron Metabolism Disorders, Movement Disorders, Neuroaxonal Dystrophies.
- psychology : Iron Metabolism Disorders, Neuroaxonal Dystrophies.
- Adult, Humans, Magnetic Resonance Imaging, Male, Neuroimaging, Treatment Failure.
DOI: 10.1002/mds.25275
PubMed: 23239021
Affiliations:
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Le document en format XML
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