Zobrazeno 1 - 10
of 54
pro vyhledávání: '"anti-MDA5 antibodies"'
Autor:
Siqi Pan, Huaiya Xie, Luo Wang, Yuanzhuo Wang, Menglian Zou, Yan Xu, Xinlun Tian, Junping Fan, Jinglan Wang
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
With the widespread use of immune checkpoint inhibitors to treat various cancers, pulmonary toxicity has become a topic of increasing concern. Anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibodies are strongly associated with rapidly
Externí odkaz:
https://doaj.org/article/bafcfdc553d3498983b96836ba159236
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundClinically amyopathic dermatomyositis (CADM) is a distinct subtype of dermatomyositis (DM) characterized by typical DM cutaneous findings but with minimal or no evidence of myositis. It possesses unique features different from classic DM (C
Externí odkaz:
https://doaj.org/article/caa19f6f04144ff4a95e345c2251863a
Publikováno v:
Diagnostics, Vol 13, Iss 24, p 3621 (2023)
We aimed to dissociate the autoantibody response against the Ro52 protein in patients with anti-synthetase or anti-melanoma differentiation-associated gene 5 (MDA5) antibodies to explore the potential roles of different anti-Ro52 autoantibody respons
Externí odkaz:
https://doaj.org/article/3ff1f4a88a914f0d92ab1cbe6b113f93
Akademický článek
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Autor:
Asami Fujii, Yuki H. Mizutani, Miho Kawamura, Kanako Matusyama, Yoko Mizutani, En Shu, Mariko Seishima
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 4, Iss 3, Pp 50-56 (2021)
Abstract Objectives Dermatomyositis (DM) is an autoimmune disease that presents with a wide variety of clinical manifestations. Patients with DM or clinically amyopathic dermatomyositis (CADM) with antimelanoma differentiation‐associated protein 5
Externí odkaz:
https://doaj.org/article/3cbafb92f5a4488885a6f2d0691e7b46
Publikováno v:
Clinics and Practice, Vol 11, Iss 2, Pp 235-240 (2021)
Anti-MDA5 antibodies-associated amyopathic dermatomyositisis a rare autoimmune disease that involve polyarthritis, cutaneous and pulmonary manifestations. The development of rapidly progressing interstitial lung disease is a life-threatening complica
Externí odkaz:
https://doaj.org/article/913c9402518e4e64a471eb1ca4887ca8
Autor:
Anca Bobirca, Cristina Alexandru, Anca Emanuela Musetescu, Florin Bobirca, Anca Teodora Florescu, Magdalena Constantin, Tiberiu Tebeica, Alesandra Florescu, Sebastian Isac, Mihai Bojinca, Ioan Ancuta
Publikováno v:
Life, Vol 12, Iss 8, p 1108 (2022)
Clinically amyopathic Dermatomyositis (CADM) is a rare subtype of idiopathic inflammatory myositis, associated with no muscular manifestations, which is more frequent in Asian women. Anti-melanoma differentiation-associated gene 5 (MDA5) antibodies a
Externí odkaz:
https://doaj.org/article/af572fb6593b46fa9d09f3c278ef2222
Akademický článek
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Akademický článek
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Autor:
Enrico Fuzzi, Mariele Gatto, Margherita Zen, Chiara Franco, Elisabetta Zanatta, Anna Ghirardello, Andrea Doria
Publikováno v:
Current Opinion in Rheumatology. 34:365-373
This review summarizes the recent developments about anti-MDA5 antibody positive dermatomyositis with a focus on its pathogenesis, clinical features and treatment options of rapidly progressive interstitial lung disease, its most ominous complication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d10a918ab99c7d6bf6d7cd5fc6dae4fe
https://doi.org/10.1097/bor.0000000000000908
https://doi.org/10.1097/bor.0000000000000908