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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1989-1-11
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0513-5796
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
278-85
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:3195160-Axons,
pubmed-meshheading:3195160-Child,
pubmed-meshheading:3195160-Demyelinating Diseases,
pubmed-meshheading:3195160-Facial Paralysis,
pubmed-meshheading:3195160-Female,
pubmed-meshheading:3195160-Hereditary Sensory and Motor Neuropathy,
pubmed-meshheading:3195160-Humans,
pubmed-meshheading:3195160-Sural Nerve
|
pubmed:year |
1988
|
pubmed:articleTitle |
A case of progressive hypertrophic neuropathy in childhood with facial diplegia (Dejerine-Sottas disease).
|
pubmed:publicationType |
Journal Article,
Case Reports
|