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Mathieu Jablonski

Explore the profile of Mathieu Jablonski including associated specialties, affiliations and a list of published articles. Areas
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Articles 15
Citations 477
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Recent Articles
1.
Pellefigues C, Dema B, Lamri Y, Saidoune F, Chavarot N, Loheac C, et al.
Nat Commun . 2018 Feb; 9(1):725. PMID: 29463843
In systemic lupus erythematosus (SLE), autoantibody production can lead to kidney damage and failure, known as lupus nephritis. Basophils amplify the synthesis of autoantibodies by accumulating in secondary lymphoid organs....
2.
Dauvergne M, Moktefi A, Rabant M, Vigneau C, Kofman T, Burtey S, et al.
Medicine (Baltimore) . 2015 Jul; 94(30):e1243. PMID: 26222864
The association between membranous nephropathy (MN) and immunological disorder-related liver disease has not been extensively investigated, and the specific features of this uncommon association, if any, remain to be determined.We...
3.
Papista C, Lechner S, Ben Mkaddem S, LeStang M, Abbad L, Bex-Coudrat J, et al.
Kidney Int . 2015 Mar; 88(2):276-85. PMID: 25807036
IgA1 complexes containing deglycosylated IgA1, IgG autoantibodies, and a soluble form of the IgA receptor (sCD89), are hallmarks of IgA nephropathy (IgAN). Food antigens, notably gluten, are associated with increased...
4.
Dema B, Charles N, Pellefigues C, Ricks T, Suzuki R, Jiang C, et al.
J Exp Med . 2014 Oct; 211(11):2159-68. PMID: 25267791
The (patho)physiological role of IgE in nonallergic inflammatory diseases is not well understood. Here, we explored the effect of IgE deficiency on the inflammatory response in FcγRIIB-deficient mice as well...
5.
Marinozzi M, Vergoz L, Rybkine T, Ngo S, Bettoni S, Pashov A, et al.
J Am Soc Nephrol . 2014 Mar; 25(9):2053-65. PMID: 24652797
Atypical hemolytic uremic syndrome (aHUS) is a genetic ultrarare renal disease associated with overactivation of the alternative pathway of complement. Four gain-of-function mutations that form a hyperactive or deregulated C3...
6.
Dema B, Pellefigues C, Hasni S, Gault N, Jiang C, Ricks T, et al.
PLoS One . 2014 Mar; 9(2):e90424. PMID: 24587356
The presence of autoantibodies in systemic lupus erythematosus, particularly those of the IgG subclass, have long been associated with disease onset and activity. Here we explored the prevalence of autoreactive...
7.
Bienaime F, Dragon-Durey M, Regnier C, Nilsson S, Kwan W, Blouin J, et al.
Kidney Int . 2009 Dec; 77(4):339-49. PMID: 20016463
Genetic studies have shown that mutations of complement inhibitors such as membrane cofactor protein, Factors H, I, or B and C3 predispose patients to atypical hemolytic uremic syndrome (aHUS). Factor...
8.
Roumenina L, Jablonski M, Hue C, Blouin J, Dimitrov J, Dragon-Durey M, et al.
Blood . 2009 Jul; 114(13):2837-45. PMID: 19584399
Complement is a major innate immune defense against pathogens, tightly regulated to prevent host tissue damage. Atypical hemolytic uremic syndrome (aHUS) is characterized by endothelial damage leading to renal failure...
9.
Yahiaoui Y, Jablonski M, Hubert D, Mosnier-Pudar H, Noel L, Stern M, et al.
Clin J Am Soc Nephrol . 2009 May; 4(5):921-8. PMID: 19406970
Background And Objectives: Clinically relevant kidney involvement is uncommonly described in adult patients with cystic fibrosis (CF). We sought to report on a series of patients with CF and kidney...
10.
Fakhouri F, Jablonski M, Lepercq J, Blouin J, Benachi A, Hourmant M, et al.
Blood . 2008 Jul; 112(12):4542-5. PMID: 18658028
The HELLP syndrome, defined by the existence of hemolysis, elevated liver enzymes, and low platelet count, is a serious complication of pregnancy-related hypertensive disorders and shares several clinical and biologic...