Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-4-23
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1469-8749
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
52
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
103-4
pubmed:meshHeading
pubmed-meshheading:19811514-Alleles, pubmed-meshheading:19811514-Base Sequence, pubmed-meshheading:19811514-Brain, pubmed-meshheading:19811514-Brain Edema, pubmed-meshheading:19811514-Calcium Channels, pubmed-meshheading:19811514-Child, Preschool, pubmed-meshheading:19811514-DNA Mutational Analysis, pubmed-meshheading:19811514-Developmental Disabilities, pubmed-meshheading:19811514-Dominance, Cerebral, pubmed-meshheading:19811514-Epilepsy, Post-Traumatic, pubmed-meshheading:19811514-Exons, pubmed-meshheading:19811514-Female, pubmed-meshheading:19811514-Genetic Testing, pubmed-meshheading:19811514-Head Injuries, Closed, pubmed-meshheading:19811514-Humans, pubmed-meshheading:19811514-Magnetic Resonance Imaging, pubmed-meshheading:19811514-Migraine with Aura, pubmed-meshheading:19811514-Mutation, Missense, pubmed-meshheading:19811514-Neurologic Examination
pubmed:year
2010
pubmed:articleTitle
Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.
pubmed:publicationType
Letter, Case Reports