Zobrazeno 1 - 10
of 893
pro vyhledávání: '"M. Moutsopoulos"'
Autor:
Tae Sung Kim, Niki M. Moutsopoulos
Publikováno v:
Experimental and Molecular Medicine, Vol 56, Iss 5, Pp 1055-1065 (2024)
Abstract Neutrophils perform essential functions in antimicrobial defense and tissue maintenance at mucosal barriers. However, a dysregulated neutrophil response and, in particular, the excessive release of neutrophil extracellular traps (NETs) are i
Externí odkaz:
https://doaj.org/article/5620c10a5662494eb26e593bc6dff10e
Autor:
Vasiliki Koulouri, Athanasios-Dimitrios Bakasis, Nikolaos Marketos, Kyriaki Tavernaraki, Mayra Giannelou, Haralampos M. Moutsopoulos, Clio P. Mavragani
Publikováno v:
Journal of Translational Autoimmunity, Vol 6, Iss , Pp 100183- (2023)
Systemic sclerosis (SSc) has been classically linked to interstitial lung disease (ILD) development, often in association with specific SSc autoantibodies. In the present report, we aimed to estimate the prevalence of SSc autoantibodies in 60 seropos
Externí odkaz:
https://doaj.org/article/c473d23386404d6e9cf1bb406a95b152
Publikováno v:
Arrhythmia & Electrophysiology Review, Vol 10, Iss 1, Pp 17-25 (2021)
Externí odkaz:
https://doaj.org/article/b54ed924a7094c03b7702c262adae6b3
Autor:
Georgios Boutzios, Eleni Koukoulioti, Andreas V. Goules, Ioannis Kalliakmanis, Ilias Giovannopoulos, Panayiotis Vlachoyiannopoulos, Haralampos M. Moutsopoulos, Athanasios G. Tzioufas
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundHashimoto thyroiditis (HT) is an autoimmune disease which may result in extensive damage of the thyroid gland. Chronic atrophic gastritis (CAG), is the most frequent HT-associated disorder, with anti-parietal cell autoantibodies (APCA) bein
Externí odkaz:
https://doaj.org/article/1bd115ffc3e44640bf39f9163000fc46
Genetic Variants of the BAFF Gene and Risk of Fatigue Among Patients With Primary Sjögren’s Syndrome
Autor:
Christina-Maria Flessa, Evangelia Zampeli, Maria-Eleftheria Evangelopoulos, Vasilis Natsis, Iris L. A. Bodewes, Erika Huijser, Marjan A. Versnel, Haralampos M. Moutsopoulos, Clio P. Mavragani
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Background/PurposePrimary Sjögren’s Syndrome (SS) is characterized by B lymphocyte hyperactivity with B cell activating factor (BAFF) acting as an important regulator. Single Nucleotide Polymorphisms (SNPs) of the BAFF gene have been implicated in
Externí odkaz:
https://doaj.org/article/15fb7d63c5604ccfbb1fe214b2e21159
Autor:
Konstantina D. Kourou, Vasileios C. Pezoulas, Eleni I. Georga, Themis Exarchos, Costas Papaloukas, Michalis Voulgarelis, Andreas Goules, Andrianos Nezos, Athanasios G. Tzioufas, Earalampos M. Moutsopoulos, Clio Mavragani, Dimitrios I. Fotiadis
Publikováno v:
IEEE Open Journal of Engineering in Medicine and Biology, Vol 1, Pp 49-56 (2020)
Lymphoma development constitutes one of the most serious clinico-pathological manifestations of patients with Sjögren's Syndrome (SS). Over the last decades the risk for lymphomagenesis in SS patients has been studied aiming to identify novel bioma
Externí odkaz:
https://doaj.org/article/2d633b63df074461851f80840e7a0cf9
Lipoprotein-Associated Phospholipase A2: A Novel Contributor in Sjögren’s Syndrome-Related Lymphoma?
Autor:
Adrianos Nezos, Charalampos Skarlis, Anna Psarrou, Konstantinos Markakis, Panagiotis Garantziotis, Asimina Papanikolaou, Fotini Gravani, Michael Voulgarelis, Athanasios G. Tzioufas, Michael Koutsilieris, Haralampos M. Moutsopoulos, Eleni Kotsifaki, Clio P. Mavragani
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundB-cell non-Hodgkin’s lymphoma (B-NHL) is one of the major complications of primary Sjögren’s syndrome (SS). Chronic inflammation and macrophages in SS minor salivary glands have been previously suggested as significant predictors for l
Externí odkaz:
https://doaj.org/article/a76ab592f8a348f4aaddce5cf22d429b
Autor:
Laurie Brenchley, Elise M. N. Ferré, Monica M. Schmitt, Pamela J. Gardner, Michail S. Lionakis, Niki M. Moutsopoulos
Publikováno v:
Frontiers in Dental Medicine, Vol 2 (2021)
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), also known as autoimmune polyglandular syndrome type 1 (APS-1), is a rare genetic disorder caused most often by biallelic mutations in the AIRE gene. Classic clinical findings o
Externí odkaz:
https://doaj.org/article/178aa349bec14c4495acd79ac0799228
Autor:
Haralampos M. Moutsopoulos
Publikováno v:
Journal of Translational Autoimmunity, Vol 4, Iss , Pp 100129- (2021)
Until the etiopathogenic factor(s) of autoimmune and autoinflammatory rheumatic disorders will be identified, their classification into entities will continue. However, their similar clinical manifestations, overlapping syndromes, evolution from one
Externí odkaz:
https://doaj.org/article/a794941b412c4a3fa15cdd29f74541ae
Autor:
Andreas V. Goules, Ourania D. Argyropoulou, Vasileios C. Pezoulas, Loukas Chatzis, Elena Critselis, Saviana Gandolfo, Francesco Ferro, Marco Binutti, Valentina Donati, Sara Zandonella Callegher, Aliki Venetsanopoulou, Evangelia Zampeli, Maria Mavrommati, Paraskevi V. Voulgari, Themis Exarchos, Clio P. Mavragani, Chiara Baldini, Fotini N. Skopouli, Dimitrios I. Fotiadis, Salvatore De Vita, Haralampos M. Moutsopoulos, Athanasios G. Tzioufas
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
ObjectivesTo study the clinical, serological and histologic features of primary Sjögren’s syndrome (pSS) patients with early (young ≤35 years) or late (old ≥65 years) onset and to explore the differential effect on lymphoma development.Methods
Externí odkaz:
https://doaj.org/article/481d5fea16b740e09ceceae1d046e364