Clinically probable multiple system atrophy with predominant parkinsonism associated with myotonic dystrophy type 2.
Identifieur interne : 002679 ( Ncbi/Curation ); précédent : 002678; suivant : 002680Clinically probable multiple system atrophy with predominant parkinsonism associated with myotonic dystrophy type 2.
Auteurs : Shen-Yang Lim ; Pettarusp Wadia ; Gregor K. Wenning ; Anthony E. LangSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2009.
English descriptors
- KwdEn :
- Brain (pathology), Humans, Magnetic Resonance Imaging (methods), Male, Middle Aged, Multiple System Atrophy (complications), Multiple System Atrophy (diagnosis), Multiple System Atrophy (genetics), Myotonic Disorders (complications), Myotonic Disorders (diagnosis), Myotonic Disorders (genetics), Parkinsonian Disorders (complications), Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics), RNA-Binding Proteins (genetics).
- MESH :
- chemical , genetics : RNA-Binding Proteins.
- complications : Multiple System Atrophy, Myotonic Disorders, Parkinsonian Disorders.
- diagnosis : Multiple System Atrophy, Myotonic Disorders, Parkinsonian Disorders.
- genetics : Multiple System Atrophy, Myotonic Disorders, Parkinsonian Disorders.
- methods : Magnetic Resonance Imaging.
- pathology : Brain.
- Humans, Male, Middle Aged.
DOI: 10.1002/mds.22625
PubMed: 19441131
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