Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children.
about
Natural history of mevalonate kinase deficiency: a literature reviewNeonatal hepatitis as first manifestation of hyperimmunoglobulinemia d syndromeInheritance of autoinflammatory diseases: shifting paradigms and nomenclature.Current advances in the understanding and treatment of mevalonate kinase deficiency.Geoepidemiology and Immunologic Features of Autoinflammatory Diseases: a Comprehensive Review.Febrile attacks triggered by milk allergy in an infant with mevalonate kinase deficiency.Anti-inflammatory and cytoprotective effects of a squalene synthase inhibitor, TAK-475 active metabolite-I, in immune cells simulating mevalonate kinase deficiency (MKD)-like condition.Splicing mutation in MVK is a cause of porokeratosis of Mibelli.Hyper Immunoglobulin D syndrome (HIDS): understanding what it is like to live with this rare condition.
P2860
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P2860
Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Incidence and clinical feature ...... mutations in German children.
@en
type
label
Incidence and clinical feature ...... mutations in German children.
@en
prefLabel
Incidence and clinical feature ...... mutations in German children.
@en
P2093
P2860
P1476
Incidence and clinical feature ...... mutations in German children.
@en
P2093
R von Kries
S Stojanov
P2860
P2888
P304
P356
10.1007/S00296-011-2180-8
P577
2011-10-30T00:00:00Z
P5875
P6179
1009585700