A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy-Reference-Cited by-同舟云学术

A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy

Published:2015 Issue:1 Volume:10 Page:11
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Zanichelli Andrea,Arcoleo Francesco,Barca Maria,Borrelli Paolo,Bova Maria,Cancian Mauro,Cicardi Marco,Cillari Enrico,De Carolis Caterina,De Pasquale Tiziana,Del Corso Isabella,Di Rocco Paola,Guarino Maria,Massaro Ilaria,Minale Paola,Montinaro Vincenzo,Neri Sergio,Perricone Roberto,Pucci Stefano,Quattrocchi Paolina,Rossi Oliviero,Triggiani Massimo,Zanierato Giuseppina,Zoli Alessandra

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-015-0233-x.pdf

Reference16 articles.

1. Hereditary Angioneurotic Edema: Two Genetic Variants

2. Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

3. Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema

4. Bradykinin-Mediated Angioedema

5. C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress

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