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Taio Naniwa

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Articles 60
Citations 335
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Recent Articles
11.
Naniwa T, Yamabe T, Ohmura S, Uehara K, Tamechika S, Maeda S, et al.
Int J Rheum Dis . 2022 Jun; 25(9):1003-1012. PMID: 35719030
Aim: Macrophage activation syndrome (MAS), a severe complication of systemic adult-onset Still's disease (AOSD), has been reported to occur during interleukin-6 (IL-6) inhibitor treatment. However, predictors for MAS development are...
12.
Ohmura S, Tamechika S, Miyamoto T, Kunieda K, Naniwa T
Int J Rheum Dis . 2022 Jun; 25(8):897-909. PMID: 35678075
Objective: To investigate the impact of dysphagia on long-term survival and swallowing function outcomes in patients with idiopathic inflammatory myopathy other than inclusion body myositis. Methods: We retrospectively evaluated consecutive...
13.
Azuma T, Misaki K, Kusaoi M, Suzuki Y, Higa S, Kumon Y, et al.
Mod Rheumatol . 2022 Apr; 33(2):271-278. PMID: 35389481
Objectives: We performed post-hoc analyses of the ORIGAMI study to investigate whether concomitant methotrexate (MTX) influences the clinical outcomes of abatacept in biologic-naïve patients with rheumatoid arthritis. Methods: Enrolled patients...
14.
Nishiyama H, Tajiri T, Yamabe T, Yasukawa T, Takeda N, Fukumitsu K, et al.
Intern Med . 2021 Jun; 60(22):3631-3634. PMID: 34092731
Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophilic cytoplasm antibody (ANCA)-associated vasculitis characterized by asthma and eosinophilia. Although EGPA involves multiple organs, ocular involvement is infrequent and often carries a...
15.
Tamechika S, Isogai S, Maeda S, Naniwa T, Niimi A
Case Rep Rheumatol . 2021 Apr; 2021:5561762. PMID: 33859858
A case of eosinophilic granulomatosis with polyangiitis (EGPA) in which chronic rhinosinusitis (CRS) was improved with a reduction in the myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA) titer after the addition of mepolizumab...
16.
Yamabe T, Ohmura S, Uehara K, Naniwa T
Mod Rheumatol . 2021 Mar; 32(1):169-176. PMID: 33719871
Objectives: Macrophage activation syndrome (MAS) developed under tocilizumab treatment poses a diagnostic challenge. This study aims to demonstrate the frequency and the clinical features of MAS developed in patients with...
17.
Gono T, Masui K, Nishina N, Kawaguchi Y, Kawakami A, Ikeda K, et al.
Arthritis Rheumatol . 2020 Oct; 73(4):677-686. PMID: 33118321
Objective: To establish predictive models for mortality in patients with polymyositis/dermatomyositis-associated interstitial lung disease (PM/DM-ILD) using a combination of initial serum biomarker levels. Methods: The Multicenter Retrospective Cohort of Japanese...
18.
Ohmura S, Uehara K, Yamabe T, Tamechika S, Maeda S, Naniwa T
Mod Rheumatol Case Rep . 2020 Oct; 4(2):202-207. PMID: 33086994
Macrophage activation syndrome (MAS) is a form of secondary hemophagocytic lymphohistiocytosis (HLH) and is a life-threatening complication of adult-onset Still disease. MAS has been usually treated with high-dose glucocorticoid with...
19.
Naniwa T, Uehara K, Yamabe T, Ohmura S
Mod Rheumatol Case Rep . 2020 Sep; 5(2):360-364. PMID: 32883165
Macrophage activation syndrome (MAS) is a form of secondary hemophagocytic lymphohistiocytosis and is a rapidly progressive, life-threatening complication of adult-onset Still's disease (AOSD). An anti-IL-6 receptor monoclonal antibody, tocilizumab, has...
20.
Ohmura S, Yamabe T, Naniwa T
Mod Rheumatol Case Rep . 2020 Sep; 5(1):76-81. PMID: 32867615
Anti-melanoma differentiation-associated gene 5 (MDA-5) antibodies have widely known to be associated with amyopathic dermatomyositis with rapidly progressive interstitial lung disease (ILD). Although the triple combination therapy with high-dose glucocorticoids,...