Linked Life Data

20800251

Source:http://linkedlifedata.com/resource/pubmed/id/20800251

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-2-22
pubmed:abstractText
Hereditary neuralgic amyotrophy (HNA) is a rare condition characterized by recurrent episodes of painful paralysis preferentially affecting the brachial plexus. It is often linked to a mutation in the SEPT9 gene.
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0035-3787
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 Elsevier Masson SAS. All rights reserved.
pubmed:issnType
Print
pubmed:volume
167
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
169-72
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
[Severe form of hereditary neuralgic amyotrophy without SEPT9 gene mutation].
pubmed:affiliation
Service d'explorations et pathologies neuromusculaires, hôpital Jean-Minjoz, CHU, 3, boulevard Fleming, 25030 Besançon cedex, France. acosson@chu-besancon.fr
pubmed:publicationType
Journal Article, English Abstract, Case Reports