Detalhe da pesquisa
1.
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
Hum Mutat
; 41(1): 38-57, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31517426
2.
Phospholipase A2 Receptor-Related Membranous Nephropathy and Mannan-Binding Lectin Deficiency.
J Am Soc Nephrol
; 27(12): 3539-3544, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27153925
3.
Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.
Int Arch Allergy Immunol
; 166(2): 114-20, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25790805
4.
Distinct conditions support a novel classification for bradykinin-mediated angio-oedema.
Dermatology
; 230(4): 324-31, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25720836
5.
SERPING1 and F12 combined variants in a hereditary angioedema family.
Ann Allergy Asthma Immunol
; 121(4): 500-502, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29885370
6.
Angioedema: Systemic activation process during prodromes.
Ann Allergy Asthma Immunol
; 121(2): 248-249, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29730014
7.
Complement alternative pathway activation in the course of thrombotic microangiopathy associated with adult-onset Still's disease.
Transfus Apher Sci
; 49(3): 533-4, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23562215
8.
Acquired C1-inhibitor deficiency: 7 patients treated with rituximab.
J Clin Immunol
; 32(5): 936-41, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22526593
9.
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.
Front Allergy
; 3: 835503, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35958943
10.
Benefits of hydroxychloroquine in the treatment of a patient with angioedema due to acquired C1 inhibitor deficiency.
Ann Allergy Asthma Immunol
; 114(1): 68-70, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25457864
11.
Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells.
J Immunol
; 181(7): 5158-66, 2008 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18802120
12.
Metallopeptidase activities in hereditary angioedema: effect of androgen prophylaxis on plasma aminopeptidase P.
J Allergy Clin Immunol
; 121(2): 429-33, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18158172
13.
Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
J Immunol Methods
; 338(1-2): 14-20, 2008 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-18655790
14.
Disease expression in women with hereditary angioedema.
Am J Obstet Gynecol
; 199(5): 484.e1-4, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18554570
15.
Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinoma.
Mol Immunol
; 43(14): 2161-8, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16529817
16.
Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activity.
Mol Immunol
; 85: 120-122, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28222330
17.
Acquired angioedema responding to rituximab.
Acta Derm Venereol
; 91(6): 733-4, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21691703
18.
C1 Inhibitor as a glycoprotein: The influence of polysaccharides on its function and autoantibody target.
Mol Immunol
; 71: 161-165, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26897339
19.
A nationwide study of acquired C1-inhibitor deficiency in France: Characteristics and treatment responses in 92 patients.
Medicine (Baltimore)
; 95(33): e4363, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27537564
20.
[Hereditary angioedema biological diagnosis]. / AngiÅdème héréditaire: diagnostic biologique.
Presse Med
; 44(1): 57-64, 2015 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-25511654