Detalhe da pesquisa
1.
Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria.
Blood;
141(15): 1812-1816, 2023 04 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36626252
2.
C3 Glomerulopathy With Concurrent Thrombotic Microangiopathy: Clinical and Immunological Features.
Am J Kidney Dis;
82(3): 279-289, 2023 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37061020
3.
Anti-Factor B Antibodies and Acute Postinfectious GN in Children.
J Am Soc Nephrol;
31(4): 829-840, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32034108
4.
Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy.
Am J Hematol;
95(5): 456-464, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31990387
5.
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
J Immunol;
200(7): 2464-2478, 2018 04 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29500241
6.
Atypical and secondary hemolytic uremic syndromes have a distinct presentation and no common genetic risk factors.
Kidney Int;
95(6): 1443-1452, 2019 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30982675
7.
Impact of hypertensive emergency and rare complement variants on the presentation and outcome of atypical hemolytic uremic syndrome.
Haematologica;
104(12): 2501-2511, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30890598
8.
Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.
Blood;
125(15): 2359-69, 2015 Apr 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25608561
9.
Assessing complement blockade in patients with paroxysmal nocturnal hemoglobinuria receiving eculizumab.
Blood;
125(5): 775-83, 2015 Jan 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25477495
10.
Defining the genetics of thrombotic microangiopathies.
Transfus Apher Sci;
54(2): 212-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27177491
11.
Usefulness and analytical performances of complement multiplex assay for measuring complement biomarkers in plasma.
Clin Chim Acta;
554: 117750, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38176523
12.
Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GN.
Clin J Am Soc Nephrol;
18(11): 1435-1445, 2023 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37615951
13.
Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies.
Front Immunol;
10: 1936, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31440263
14.
Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study.
Clin J Am Soc Nephrol;
14(3): 364-377, 2019 03 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30674459
15.
[Complement deficiencies and human diseases]. / Déficits en protéines du complément et pathologies humaines.
Ann Biol Clin (Paris);
72(3): 271-80, 2014.
Artigo
em Francês
| MEDLINE
| ID: mdl-24876138