about
Hereditary Angioedema as a Metabolic Liver Disorder: Novel Therapeutic Options and Prospects for Cure.Hereditary angioedema with a mutation in the plasminogen gene.Single-chain factor XII: a new form of activated factor XII.Emerging Therapies in Hereditary Angioedema.2D-LC-MS/MS to measure cleaved high-molecular-weight kininogen in human plasma as a biomarker for C1-INH-HAE.An ABC of the Warning Signs of Hereditary Angioedema.Endocan: A Novel Marker of Endothelial Dysfunction in C1-Inhibitor-Deficient Hereditary Angioedema.Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight.Immunological Rare Diseases.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
HAE Pathophysiology and Underlying Mechanisms.
@en
type
label
HAE Pathophysiology and Underlying Mechanisms.
@en
prefLabel
HAE Pathophysiology and Underlying Mechanisms.
@en
P2860
P1476
HAE Pathophysiology and Underlying Mechanisms
@en
P2093
Sandra C Christiansen
P2860
P2888
P304
P356
10.1007/S12016-016-8561-8
P577
2016-10-01T00:00:00Z
P6179
1037042389