Detalhe da pesquisa
1.
Deregulated cellular circuits driving immunoglobulins and complement consumption associate with the severity of COVID-19 patients.
Eur J Immunol
; 51(3): 634-647, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33251605
2.
Complement as a diagnostic tool in immunopathology.
Semin Cell Dev Biol
; 85: 86-97, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29292221
3.
Complement Factor D (adipsin) Levels Are Elevated in Acquired Partial Lipodystrophy (Barraquer-Simons syndrome).
Int J Mol Sci
; 22(12)2021 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34205507
4.
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
Hum Mutat
; 41(1): 38-57, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31517426
5.
Novel homozygous variants in the SERPING1 gene in two Turkish families with hereditary angioedema of recessive inheritance.
Immunol Cell Biol
; 98(8): 693-699, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445210
6.
Elevated factor H-related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy.
Kidney Int
; 92(4): 953-963, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28637589
7.
Multimarker risk stratification approach at multiple sclerosis onset.
Clin Immunol
; 181: 43-50, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28578025
8.
Mechanisms Involved in Hypersensitivity Reactions to Polysulfone Hemodialysis Membranes.
Artif Organs
; 41(11): E285-E295, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28722144
9.
Testing the Activity of Complement Convertases in Serum/Plasma for Diagnosis of C4NeF-Mediated C3 Glomerulonephritis.
J Clin Immunol
; 36(5): 517-27, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27146825
10.
Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation.
BMC Nephrol
; 16: 40, 2015 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886501
11.
Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3.
J Immunol
; 189(4): 1858-67, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22786770
12.
Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene.
Pediatr Nephrol
; 29(1): 149-53, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23982707
13.
Eculizumab in dense-deposit disease after renal transplantation.
Pediatr Nephrol
; 29(10): 2055-9, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24908321
14.
Human plasma C3 is essential for the development of memory B, but not T, lymphocytes.
J Allergy Clin Immunol
; 141(3): 1151-1154.e14, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29113906
15.
Clinical Characteristics of Patients With Acquired Partial Lipodystrophy: A Multicenter Retrospective Study.
J Clin Endocrinol Metab
; 109(3): e932-e944, 2024 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38061004
16.
Characterization and Clinical Association of Autoantibodies Against Perilipin 1 in Patients With Acquired Generalized Lipodystrophy.
Diabetes
; 72(1): 71-84, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35771980
17.
Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance.
Kidney Int
; 81(1): 56-63, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21881555
18.
Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation.
Kidney Int
; 82(10): 1084-92, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22854646
19.
Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants.
Am J Kidney Dis
; 59(5): 707-10, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22196848
20.
Clinical, biochemical, and genetic characterization of type III hereditary angioedema in 13 Northwest Spanish families.
Ann Allergy Asthma Immunol
; 109(3): 195-200.e2, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22920075