Ramsay Hunt syndrome, Unverricht‐Lundborg disease, or what?
Identifieur interne : 006434 ( Main/Exploration ); précédent : 006433; suivant : 006435Ramsay Hunt syndrome, Unverricht‐Lundborg disease, or what?
Auteurs : Harding [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 1989.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Cerebellar Ataxia, Epilepsies, Myoclonic, Myoclonic Cerebellar Dyssynergia.
- genetics : Myoclonic Cerebellar Dyssynergia.
- Diagnosis, Differential, Humans.
Url:
DOI: 10.1002/mds.870040105
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Corpus: 005006
- to stream PubMed, to step Curation: 005006
- to stream PubMed, to step Checkpoint: 004F67
- to stream Ncbi, to step Merge: 004031
- to stream Ncbi, to step Curation: 004031
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Le document en format XML
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