16344534

Source:http://linkedlifedata.com/resource/pubmed/id/16344534

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0332281, umls-concept:C1412629, umls-concept:C1865323
pubmed:issue	11
pubmed:dateCreated	2005-12-13
pubmed:abstractText	Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura, differentiated only by motor symptoms, which are absent in BM. Mutations in CACNA1A and ATP1A2 have been found in FHM. The authors detected a novel mutation in the ATP1A2 gene (R548H) in members of a family with BM, suggesting that BM and FHM may be allelic disorders.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ATP1A2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1526-632X
pubmed:author	pubmed-author:AmbrosiniAA, pubmed-author:BuzziM GMG, pubmed-author:D'OnofrioMM, pubmed-author:Di MambroAA, pubmed-author:FortiniDD, pubmed-author:GriecoG SGS, pubmed-author:MontagnaGG, pubmed-author:NappiGG, pubmed-author:NicolettiFF, pubmed-author:PierelliFF, pubmed-author:SancesGG, pubmed-author:SantorelliF MFM, pubmed-author:SchoenenJJ
pubmed:issnType	Electronic
pubmed:day	13
pubmed:volume	65
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1826-8
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:16344534-Adolescent, pubmed-meshheading:16344534-Aged, pubmed-meshheading:16344534-Brain, pubmed-meshheading:16344534-Chromosomes, Human, Pair 1, pubmed-meshheading:16344534-DNA Mutational Analysis, pubmed-meshheading:16344534-Female, pubmed-meshheading:16344534-Genetic Predisposition to Disease, pubmed-meshheading:16344534-Genetic Testing, pubmed-meshheading:16344534-Genotype, pubmed-meshheading:16344534-Humans, pubmed-meshheading:16344534-Italy, pubmed-meshheading:16344534-Male, pubmed-meshheading:16344534-Middle Aged, pubmed-meshheading:16344534-Migraine with Aura, pubmed-meshheading:16344534-Mutation, pubmed-meshheading:16344534-Mutation, Missense, pubmed-meshheading:16344534-Phenotype, pubmed-meshheading:16344534-Point Mutation, pubmed-meshheading:16344534-Sodium-Potassium-Exchanging ATPase
pubmed:year	2005
pubmed:articleTitle	Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
pubmed:affiliation	Headache Clinic, INM Neuromed, Pozzilli, Italy. anna.ambrosini@neuromed.it
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't