Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2003-7-8
pubmed:abstractText
The authors carried out clinical, histopathologic, immunocytochemical, electrophysiologic, and imaging investigations and molecular genetic analysis in seven patients with distal myopathy belonging to a Finnish family.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
8
pubmed:volume
61
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
87-92
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:12847162-Adult, pubmed-meshheading:12847162-Age of Onset, pubmed-meshheading:12847162-Aged, pubmed-meshheading:12847162-Biopsy, pubmed-meshheading:12847162-Creatine Kinase, pubmed-meshheading:12847162-Disease Progression, pubmed-meshheading:12847162-Electrodiagnosis, pubmed-meshheading:12847162-Family, pubmed-meshheading:12847162-Female, pubmed-meshheading:12847162-Finland, pubmed-meshheading:12847162-Genes, Dominant, pubmed-meshheading:12847162-Genetic Linkage, pubmed-meshheading:12847162-Hand, pubmed-meshheading:12847162-Humans, pubmed-meshheading:12847162-Leg, pubmed-meshheading:12847162-Magnetic Resonance Imaging, pubmed-meshheading:12847162-Male, pubmed-meshheading:12847162-Middle Aged, pubmed-meshheading:12847162-Muscle, Skeletal, pubmed-meshheading:12847162-Muscle Weakness, pubmed-meshheading:12847162-Muscular Dystrophies, pubmed-meshheading:12847162-Pedigree, pubmed-meshheading:12847162-Phenotype, pubmed-meshheading:12847162-Tomography, X-Ray Computed
pubmed:year
2003
pubmed:articleTitle
A distinct phenotype of distal myopathy in a large Finnish family.
pubmed:affiliation
Department of Neurology, Oulu University Hospital, Finland. ibrahim.mahjneh@vshp.fi
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't