MV2 subtype of sporadic Creutzfeldt‐Jakob disease presenting as corticobasal syndrome
Identifieur interne : 002D59 ( Main/Exploration ); précédent : 002D58; suivant : 002D60MV2 subtype of sporadic Creutzfeldt‐Jakob disease presenting as corticobasal syndrome
Auteurs : Anna Magherini [Italie] ; Roberta Pentore [Italie] ; Giuliana Galassi [Italie] ; Carlo M. Stucchi [Italie] ; Sabina Capellari [Italie] ; Piero Parchi [Italie]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-04-30.
English descriptors
- KwdEn :
- MESH :
- classification : Creutzfeldt-Jakob Syndrome.
- pathology : Cerebellum, Cerebral Cortex, Creutzfeldt-Jakob Syndrome.
- Humans, Male, Middle Aged.
Url:
DOI: 10.1002/mds.21426
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 004032
- to stream Istex, to step Curation: 004032
- to stream Istex, to step Checkpoint: 001867
- to stream PubMed, to step Corpus: 002791
- to stream PubMed, to step Curation: 002791
- to stream PubMed, to step Checkpoint: 002731
- to stream Ncbi, to step Merge: 001B48
- to stream Ncbi, to step Curation: 001B48
- to stream Ncbi, to step Checkpoint: 001B48
- to stream Main, to step Merge: 003C81
- to stream Main, to step Curation: 002D59
Le document en format XML
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<series><title level="j">Movement Disorders</title>
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