4.8 Editorial Material

The hereditary angioedema syndromes

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Allergy

Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema

Valeria Bafunno et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2018)

Article Medicine, Research & Experimental

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

Jenny Bjoerkqvist et al.

JOURNAL OF CLINICAL INVESTIGATION (2015)

Article Multidisciplinary Sciences

Activation of the factor XII-driven contact system in Alzheimer's disease patient and mouse model plasma

Daria Zamolodchikov et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)

Article Biochemistry & Molecular Biology

Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor

G Dewald et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)

Article Biochemistry & Molecular Biology

Identification and characterization of prolylcarboxypeptidase as an endothelial cell prekallikrein activator

Z Shariat-Madar et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2002)

Article Medicine, General & Internal

Hereditary angioedema with normal C1-inhibitor activity in women

K Bork et al.

LANCET (2000)