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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2008-10-15
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pubmed:abstractText |
Pediatric essential thrombocythemia (ET) is a rare and heterogenous disease entity. While several recent studies have focused on the role of the JAK2 V617F mutation in pediatric ET, the frequency of pediatric ET cases with this mutation and the associated clinical features remain unclear.
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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 |
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/CD177 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/GPI-Linked Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Isoantigens,
http://linkedlifedata.com/resource/pubmed/chemical/JAK2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Janus Kinase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1545-5017
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
802-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18802948-Adolescent,
pubmed-meshheading:18802948-Biological Markers,
pubmed-meshheading:18802948-Child,
pubmed-meshheading:18802948-Child, Preschool,
pubmed-meshheading:18802948-Cohort Studies,
pubmed-meshheading:18802948-Exons,
pubmed-meshheading:18802948-Female,
pubmed-meshheading:18802948-GPI-Linked Proteins,
pubmed-meshheading:18802948-Humans,
pubmed-meshheading:18802948-Infant,
pubmed-meshheading:18802948-Isoantigens,
pubmed-meshheading:18802948-Janus Kinase 2,
pubmed-meshheading:18802948-Male,
pubmed-meshheading:18802948-Membrane Glycoproteins,
pubmed-meshheading:18802948-Mutation,
pubmed-meshheading:18802948-Neutrophils,
pubmed-meshheading:18802948-Polymerase Chain Reaction,
pubmed-meshheading:18802948-Receptors, Cell Surface,
pubmed-meshheading:18802948-Thrombocythemia, Essential
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pubmed:year |
2008
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pubmed:articleTitle |
Frequency and clinical features of the JAK2 V617F mutation in pediatric patients with sporadic essential thrombocythemia.
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pubmed:affiliation |
Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
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pubmed:publicationType |
Journal Article
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