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期刊名:Journal of rheumatic diseases

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ISSN:2093-940X

e-ISSN:2233-4718

IF/分区:3.8/Q2

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共收录本刊相关文章索引209
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Kyung-Ann Lee,Sooyoung Kim,Ho-Yeon Song et al. Kyung-Ann Lee et al.
Objective: Although the close interactions between the epidermis and dermis of the skin have been widely explored, the skin barrier functions of the stratum corneum (SC) in patients with systemic sclerosis (SSc) and prima...
Vitaly Omelchenko,Elena Letyagina,Maxim Korolev Vitaly Omelchenko
Osteopoikilosis (OPK) is a rare benign congenital genetic-mediated sclerosing skeletal disease, characterized by the formation of osteosclerosis foci. OPK is usually clinically asymptomatic, but some patients (15%~20%) may have arthralgia a...
So-Young Bang,Seung Cheol Shim So-Young Bang
The prevalence of systemic lupus erythematosus (SLE) varies significantly based on ethnicity rather than geographic distribution; thus, the prevalence is higher in Asian, Hispanic, and Black African populations than in European populations....
Eui-Jong Kwon,Youngjae Park,Seung-Ki Kwok et al. Eui-Jong Kwon et al.
Objective: This study aimed to elucidate the clinical and laboratory differences between chronic sclerosing sialadenitis (CSS) and primary Sjögren's syndrome (pSS), highlighting CSS as a distinct pathological entity with...
Jong Gyun Ahn Jong Gyun Ahn
Pediatric vasculitis and adult vasculitis differ in several aspects. While both involve inflammation of blood vessels, pediatric vasculitis tends to present with distinct clinical features and may involve different types of blood vessels co...
Frederico Rajão Martins,Margarida Lucas Rocha,Ana Teodósio Chícharo et al. Frederico Rajão Martins et al.
Hae Ryung Kim,Seon Hee Lim,Ji Soo Park et al. Hae Ryung Kim et al.
Stimulator of interferon gene (STING)-associated vasculopathy with onset in infancy (SAVI) is an extremely rare autoinflammatory disease. We present the case of a female Korean patient with early-onset interstitial lung disease who was init...
Ji Hyoun Kim,Sang Wan Chung,Yun Jong Lee Ji Hyoun Kim
Neuro-Behçet's disease (NBD) represents a significant complication of Behçet's syndrome, potentially leading to elevated mortality and disability rates. The standard treatment for parenchymal NBD typically entails administering high-dose ...