Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-3
pubmed:dateCreated
1989-3-29
pubmed:abstractText
Eleven patients of one kindred are described with amyotrophy of the hands or pyramidal features of predominantly the legs or both. Clinical examination indicated neuronal origin of wasting and weakness of the hands, whereas electrophysiological investigations suggested motor neuropathy. It is suggested that both lower and motor neuron signs are segregating as independent autosomal dominant traits.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-510X
pubmed:author
pubmed:issnType
Print
pubmed:volume
88
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
241-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1988
pubmed:articleTitle
Amyotrophy of the hands and pyramidal features of predominantly the legs segregating within one large family.
pubmed:affiliation
Department of Neurology, University of Amsterdam, The Netherlands.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't