Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
about
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working GroupRecurrent angioedema and the threat of asphyxiation.Pediatric hereditary angioedema due to C1-inhibitor deficiency.Management of hereditary angioedema in pregnant women: a review.Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 geneA Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype AssociationHereditary Angioedema as a Metabolic Liver Disorder: Novel Therapeutic Options and Prospects for Cure.Comprehensive genetic testing for primary immunodeficiency disorders in a tertiary hospital: 10-year experience in Auckland, New ZealandInternational consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema.rhC1INH: a new drug for the treatment of attacks in hereditary angioedema caused by C1-inhibitor deficiency.New therapeutics in C1INH deficiency: a review of recent studies and advances.The new era of C1-esterase inhibitor deficiency therapy.New topics in bradykinin research.Current management options for hereditary angioedema.Therapeutic options for patients with angioedema due to C1-inhibitor deficiencies: from pathophysiology to the clinic.Therapeutic management of hereditary angioedema due to C1 inhibitor deficiency.Genetics of Hereditary Angioedema Revisited.Hereditary Angioedema Attacks: Local Swelling at Multiple Sites.C-reactive protein levels in hereditary angioedema.Outcomes of long term treatments of type I hereditary angioedema in a Turkish family.Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema.The Turkish Hereditary Angioedema Pilot Study (TURHAPS): the first Turkish series of hereditary angioedema.A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
P2860
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P2860
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Mutation screening of C1 inhib ...... nal and structural correlates.
@ast
Mutation screening of C1 inhib ...... nal and structural correlates.
@en
Mutation screening of C1 inhib ...... nal and structural correlates.
@nl
type
label
Mutation screening of C1 inhib ...... nal and structural correlates.
@ast
Mutation screening of C1 inhib ...... nal and structural correlates.
@en
Mutation screening of C1 inhib ...... nal and structural correlates.
@nl
prefLabel
Mutation screening of C1 inhib ...... nal and structural correlates.
@ast
Mutation screening of C1 inhib ...... nal and structural correlates.
@en
Mutation screening of C1 inhib ...... nal and structural correlates.
@nl
P2093
P1433
P1476
Mutation screening of C1 inhib ...... onal and structural correlates
@en
P2093
Attila Tordai
Chiara Suffritti
Emanuela Pappalardo
Lorenza Chiara Zingale
P304
P356
10.1016/J.MOLIMM.2008.05.007
P577
2008-06-30T00:00:00Z