Zobrazeno 1 - 10
of 33 494
pro vyhledávání: '"Systemic Sclerosis"'
Autor:
Beomgu Lee, Jong Seong Roh, Hoim Jeong, Yerin Kim, Jihyeon Lee, Changun Yun, Jiyoung Park, Da-sol Kim, Jungsoo Lee, Min Wook So, Aran Kim, Dong Hyun Sohn, Seung-Geun Lee
Publikováno v:
Animal Cells and Systems, Vol 28, Iss 1, Pp 152-160 (2024)
ABSTRACTSystemic sclerosis (SSc) is a chronic autoimmune disease characterized by skin and internal organ fibrosis and obliterative vasculopathy. Few effective treatments are currently available for fibrosis in SSc, therefore, demand persists for nov
Externí odkaz:
https://doaj.org/article/2bf7767d0625499d8c5425daca7c30e5
Publikováno v:
BMC Biotechnology, Vol 24, Iss 1, Pp 1-15 (2024)
Abstract Background Exploration of whether circRNAs in the skin of systemic sclerosis (SSc) model mice interact with 4E-BP1 protein to mediate the mTOR signaling pathway to regulate SSc fibrosis is crucial to identify homologous human circRNAs as mar
Externí odkaz:
https://doaj.org/article/09b0f8a7f9784e689299f7e9d32dd373
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Objectives were to assess the mouth opening ability (MOA) among patients with systemic sclerosis (SSc) in comparison to a healthy control population. The impact of microstomia (decrease in any of the MOA parameters) on physical pe
Externí odkaz:
https://doaj.org/article/44f833996cc34563b0506f1494f9fb53
Autor:
Xinyu Tong, Huilin He, Shihan Xu, Rui Shen, Zihan Ning, Xiaofeng Zeng, Qian Wang, Dong Xu, Zuo-Xiang He, Xihai Zhao
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-11 (2024)
Abstract Background Neuropsychiatric manifestations, such as cognitive impairment, are relatively prevalent in systemic sclerosis (SSc) patients. This study aimed to investigate the resting state (RS) functional alternations of SSc patients and the p
Externí odkaz:
https://doaj.org/article/b181f91cc2c4414f9502e026b23d7d0c
Publikováno v:
Clinical Dermatology Review, Vol 8, Iss 4, Pp 371-374 (2024)
Juvenile systemic sclerosis (JSSc) is a highly uncommon, chronic connective tissue disorder that affects multiple systems, marked by progressive deposition of collagen under the dermis, and various deep organs. Delay in diagnosis can cause irreversib
Externí odkaz:
https://doaj.org/article/4bf250131c644e72b22559e1c64260c8
Autor:
Nicoletta Del Papa, Silvia Cavalli, Andrea Rindone, Francesco Onida, Giorgia Saporiti, Antonina Minniti, Maria Rosa Pellico, Claudia Iannone, Giorgia Trignani, Nicoletta D’Angelo, Manuel Sette, Raffaella Greco, Claudio Vitali, Roberto Caporali
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-10 (2024)
Abstract Background Autologous haematopoietic stem cell transplantation (AHSCT) is more effective than conventional immunosuppressive therapies (CIT) in improving the outcome of patients with rapidly progressive diffuse cutaneous systemic sclerosis (
Externí odkaz:
https://doaj.org/article/5c4ae2c1609e4fdc8b9283e078126e30
Autor:
Shyam Nathan, Yifei Wang, Matthew D’ambrosio, Reeba Paul, Huimin Lyu, Denis Delic, Tom Bretschneider, Kimberly Falana, Li Li, Preethi Vijayaraj
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Systemic sclerosis (SSc) is an autoimmune disease characterized by vasculopathy, immune dysregulation, and systemic fibrosis. Research on SSc has been hindered largely by lack of relevant models to study the progressive nature of the disease
Externí odkaz:
https://doaj.org/article/4f95fef11cd74158aa182d9c109c859b
Publikováno v:
Case Reports in Ophthalmology, Vol 15, Iss 1, Pp 710-716 (2024)
This is an observational case report to detail a novel case of scleroderma renal crisis presenting as bilateral exudative retinal detachments in a patient with newly diagnosed systemic sclerosis. An otherwise healthy 58-year-old female presented prim
Externí odkaz:
https://doaj.org/article/4c60ce50ff5c43e08d117d656991cd82
Autor:
Kristine Ivanova, Olga Ribakova, Anna Mihailova, Evelina Mozeitovica, Anda Kadisa, Julija Zepa, Viktorija Kenina, Natalja Kurjane, Inita Bulina
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Systemic sclerosis (SSc) is considered by many to be one of the most severe autoimmune rheumatic diseases with lower prevalence observed in Northern Europe. No previous studies on the prevalence of SSc in Latvia have been conducte
Externí odkaz:
https://doaj.org/article/c540456a22c240b6a63d34e9e2c33b0e
Autor:
Ursula Heilmeier, Daria Feldmann, Andrew Leynes, Magdalena Seng, Ilona Jandova, Marius Keute, Florian Kollert, Reinhard Edmund Voll, Stephanie Finzel
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundVasculopathy is a hallmark of systemic sclerosis (SSc) putting patients at an increased risk of cardiovascular disease. Approximately 20–25% of all SSc patients show prolonged elevated C-reactive protein (CRP) levels and thus signs of chr
Externí odkaz:
https://doaj.org/article/93a5da63fc2e497b8afc0c680613bc19