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1.
Reduction in hypoxia-reoxygenation-induced myocardial mitochondrial damage with exogenous methane.
J Cell Mol Med
; 25(11): 5113-5123, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33942485
2.
Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome.
J Am Soc Nephrol
; 29(3): 1020-1029, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29282226
3.
Risk factors of non-specific spinal pain in childhood.
Eur Spine J
; 27(5): 1119-1126, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29450642
4.
Structural Basis for the Function of Complement Component C4 within the Classical and Lectin Pathways of Complement.
J Immunol
; 194(11): 5488-96, 2015 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25911760
5.
High rate of in-stent restenosis after coronary intervention in carriers of the mutant mannose-binding lectin allele.
BMC Cardiovasc Disord
; 17(1): 4, 2017 01 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28056798
6.
The major autoantibody epitope on factor H in atypical hemolytic uremic syndrome is structurally different from its homologous site in factor H-related protein 1, supporting a novel model for induction of autoimmunity in this disease.
J Biol Chem
; 290(15): 9500-10, 2015 Apr 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-25659429
7.
Hemolytic uremic syndrome with Mycoplasma pneumoniae infection and membrane cofactor protein mutation case report.
Przegl Lek
; 73(11): 862-4, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-29693967
8.
Novel duplication in the F12 gene in a patient with recurrent angioedema.
Clin Immunol
; 149(1): 142-5, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23994767
9.
Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis.
Br J Haematol
; 160(2): 216-9, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23078005
10.
The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome.
Nephrol Dial Transplant
; 28(9): 2237-45, 2013 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-23787556
11.
Hemolytic uremic syndrome in the setting of COVID-19 successfully treated with complement inhibition therapy: An instructive case report of a previously healthy toddler and review of literature.
Front Pediatr
; 11: 1092860, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36873657
12.
Pregnancy in Complement-Mediated Thrombotic Microangiopathy: Maternal and Neonatal Outcomes.
Kidney Med
; 5(7): 100669, 2023 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-37492116
13.
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema.
Clin Transl Allergy
; 13(11): e12317, 2023 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-38006386
14.
Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups.
Front Immunol
; 14: 1162171, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37051252
15.
ACTH-induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non-functional adrenal incidentaloma.
Clin Endocrinol (Oxf)
; 76(4): 478-84, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21967755
16.
Complement Genetics for the Practicing Allergist Immunologist: Focus on Complement Deficiencies.
J Allergy Clin Immunol Pract
; 10(7): 1703-1711, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35272074
17.
MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy.
Front Immunol
; 13: 985766, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36189289
18.
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema.
Front Allergy
; 3: 836465, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35386643
19.
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency-Experience From the Hungarian Angioedema Center of Reference and Excellence.
Front Allergy
; 3: 860355, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35769571
20.
Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report.
Front Immunol
; 13: 1001366, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36275662