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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
2010-9-14
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pubmed:abstractText |
Hemiplegic migraine (HM) is a rare subtype of migraine with aura that may occur as a familial (FHM) or sporadic condition (SHM). Screening of FHM genes in previous series of patients with SHM detected a very low proportion of mutated patients. In this study, we investigated the FHM genes in patients with an early onset sporadic form of HM (onset before 16 years).
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/ATP1A2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/CACNA1A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase,
http://linkedlifedata.com/resource/pubmed/chemical/sodium channel, voltage-gated...
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1526-632X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
14
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
967-72
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pubmed:dateRevised |
2010-11-24
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pubmed:meshHeading |
pubmed-meshheading:20837964-Adolescent,
pubmed-meshheading:20837964-Adult,
pubmed-meshheading:20837964-Age of Onset,
pubmed-meshheading:20837964-Calcium Channels,
pubmed-meshheading:20837964-Child,
pubmed-meshheading:20837964-Computational Biology,
pubmed-meshheading:20837964-DNA,
pubmed-meshheading:20837964-Female,
pubmed-meshheading:20837964-Gene Frequency,
pubmed-meshheading:20837964-Hemiplegia,
pubmed-meshheading:20837964-Humans,
pubmed-meshheading:20837964-Male,
pubmed-meshheading:20837964-Migraine Disorders,
pubmed-meshheading:20837964-Mutation,
pubmed-meshheading:20837964-Nerve Tissue Proteins,
pubmed-meshheading:20837964-Neuropsychological Tests,
pubmed-meshheading:20837964-Sodium Channels,
pubmed-meshheading:20837964-Sodium-Potassium-Exchanging ATPase,
pubmed-meshheading:20837964-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
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pubmed:affiliation |
Laboratoire de Génétique Moléculaire, APHP-Hôpital Lariboisière, Paris, France. florence.riant@lrb.aphp.fr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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