Detalhe da pesquisa
1.
Alpha-synuclein dynamics bridge Type-I Interferon response and SARS-CoV-2 replication in peripheral cells.
Biol Res
; 57(1): 2, 2024 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38191441
2.
IgM Autoantibodies to Complement Factor H in Atypical Hemolytic Uremic Syndrome.
J Am Soc Nephrol
; 32(5): 1227-1235, 2021 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33712527
3.
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.
Clin Mol Allergy
; 19(1): 3, 2021 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33827715
4.
Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Int J Mol Sci
; 21(13)2020 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32610551
5.
A transcriptomics study of hereditary angioedema attacks.
J Allergy Clin Immunol
; 142(3): 883-891, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29729940
6.
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family.
J Hum Genet
; 61(4): 295-300, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657938
7.
Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop).
J Thromb Thrombolysis
; 50(1): 233-236, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712947
8.
Platelet Microvesicles, Inflammation, and Coagulation Markers: A Pilot Study.
Hematol Rep
; 15(4): 684-695, 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38132277
9.
Anti-C1-Inhibitor Autoantibody Detection by ELISA.
Methods Mol Biol
; 2227: 115-120, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33847936
10.
C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress.
Trends Mol Med
; 15(2): 69-78, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19162547
11.
The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency.
Int Immunopharmacol
; 82: 106304, 2020 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32114411
12.
Circulating endothelial progenitors are increased in COVID-19 patients and correlate with SARS-CoV-2 RNA in severe cases.
J Thromb Haemost
; 18(10): 2744-2750, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32762140
13.
Acid Sphingomyelinase Downregulation Enhances Mitochondrial Fusion and Promotes Oxidative Metabolism in a Mouse Model of Melanoma.
Cells
; 9(4)2020 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32244541
14.
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
Mol Immunol
; 45(13): 3536-44, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18586324
15.
Current and emerging biologics for the treatment of hereditary angioedema.
Expert Opin Biol Ther
; 19(6): 517-526, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30912460
16.
Alpha-synuclein dynamics bridge Type-I Interferon response and SARS-CoV-2 replication in peripheral cells
Biol. Res
; 57: 2-2, 2024. ilus, graf
Artigo
em Inglês
| LILACS | ID: biblio-1550057
17.
Recombinant human C1 esterase inhibitor (Conestat alfa) for prophylaxis to prevent attacks in adult and adolescent patients with hereditary angioedema.
Expert Rev Clin Immunol
; 14(9): 707-718, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30021471
18.
Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency.
J Allergy Clin Immunol Pract
; 11(3): 963-965.e1, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36379410
19.
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight.
Sci Rep
; 8(1): 977, 2018 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29343682
20.
Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency.
J Allergy Clin Immunol Pract
; 5(5): 1307-1313, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28284781