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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2008-1-30
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pubmed:abstractText |
Presenting the case of unusual onset hypokalemic periodic paralysis (HypoPP) where myopathy had developed two years before paralysis occurred.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1896-1126
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
52 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
155-7
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pubmed:dateRevised |
2008-5-15
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pubmed:meshHeading |
pubmed-meshheading:18229654-Adolescent,
pubmed-meshheading:18229654-Age of Onset,
pubmed-meshheading:18229654-Calcium Channels,
pubmed-meshheading:18229654-Child,
pubmed-meshheading:18229654-Child, Preschool,
pubmed-meshheading:18229654-Female,
pubmed-meshheading:18229654-Humans,
pubmed-meshheading:18229654-Male,
pubmed-meshheading:18229654-Mutation,
pubmed-meshheading:18229654-Paralysis, Hyperkalemic Periodic,
pubmed-meshheading:18229654-Pedigree
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pubmed:year |
2007
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pubmed:articleTitle |
Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutation.
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pubmed:affiliation |
Chair and Department of Developmental Neurology, Pozna? University of Medical Sciences, Poland. awwiktor@amp.edu.pl
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pubmed:publicationType |
Journal Article,
Case Reports
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