Detalhe da pesquisa
1.
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2021 revision and update.
Allergy
; 77(7): 1961-1990, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35006617
2.
Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.
J Allergy Clin Immunol
; 148(4): 1041-1048, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33508266
3.
Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor.
N Engl J Med
; 376(12): 1131-1140, 2017 03 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28328347
4.
Hereditary angioedema in children and adolescents - A consensus update on therapeutic strategies for German-speaking countries.
Pediatr Allergy Immunol
; 31(8): 974-989, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32524650
5.
Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
J Dtsch Dermatol Ges
; 18(3): 215-223, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32065705
6.
[Hereditary angioedema]. / Hereditäres Angioödem.
Internist (Berl)
; 60(9): 987-995, 2019 Sep.
Artigo
em Alemão
| MEDLINE | ID: mdl-31363809
7.
Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels.
J Allergy Clin Immunol
; 137(6): 1822-1829.e1, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26395818
8.
Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema.
Int Arch Allergy Immunol
; 170(2): 101-7, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27463190
9.
Efficacy of Different Medical Therapies for the Treatment of Acute Laryngeal Attacks of Hereditary Angioedema due to C1-esterase Inhibitor Deficiency.
J Emerg Med
; 50(4): 567-80.e1, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26826769
10.
Definition, aims, and implementation of GA2 LEN/HAEi Angioedema Centers of Reference and Excellence.
Allergy
; 75(8): 2115-2123, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32248571
11.
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
12.
Efficacy of C1 esterase inhibitor concentrate in treatment of cutaneous attacks of hereditary angioedema.
Allergy Asthma Proc
; 36(3): 218-24, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25803207
13.
Hereditäres Angioödem in einer Familie mit spezifischen Mutationen sowohl im Plasminogen- als auch im SERPING1-Gen.
J Dtsch Dermatol Ges
; 18(3): 215-224, 2020 Mar.
Artigo
em Alemão
| MEDLINE | ID: mdl-32130763
14.
Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin.
Allergy
; 74(12): 2479-2481, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31087670
15.
Genotype-phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency.
Allergy
; 74(5): 1013-1016, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30556912
16.
Antibody-mediated inhibition of FXIIa blocks downstream bradykinin generation.
J Allergy Clin Immunol
; 142(4): 1355-1358, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29936101
17.
Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema.
N Engl J Med
; 363(6): 532-41, 2010 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20818888
18.
Treatment with C1-esterase inhibitor concentrate in type I or II hereditary angioedema: a systematic literature review.
Allergy Asthma Proc
; 34(4): 312-327, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23710659
19.
Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency.
J Allergy Clin Immunol
; 130(3): 692-7, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22841766
20.
Reply.
J Allergy Clin Immunol
; 139(5): 1720-1721, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28318557