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Chihiro Terai

Explore the profile of Chihiro Terai including associated specialties, affiliations and a list of published articles. Areas
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Articles 34
Citations 218
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Recent Articles
1.
Kurihara I, Terai C, Yabe H, Sugawara H
Am J Case Rep . 2022 Nov; 23:e937201. PMID: 36336892
BACKGROUND Nephrotic syndrome caused by minimal mesangial lupus nephritis is considered rare. Nephrotic syndrome can be caused by minimal mesangial lupus nephritis with diffuse epithelial foot-process effacement and lupus podocytopathy....
2.
Watanabe E, Kato K, Gono T, Chiba E, Terai C, Kotake S
Rheumatology (Oxford) . 2020 Aug; 60(1):322-332. PMID: 32770187
Objectives: Galectin-3 is involved in various biological activities, including immune activations and fibrosis. Idiopathic inflammatory myopathies (IIMs) are autoimmune diseases of unknown aetiology, often complicated by interstitial lung disease (ILD)....
3.
Watanabe E, Gono T, Kuwana M, Terai C
Rheumatology (Oxford) . 2019 Aug; 59(3):586-593. PMID: 31410476
Objective: The aim of this study was to clarify predictive factors for sustained remission in adult patients with PM/DM, particularly focusing on stratification by myositis-specific autoantibodies (MSAs). Methods: A total...
4.
Watanabe E, Tanaka A, Sugawara H, Nishina K, Yabe H, Gono T, et al.
Am J Case Rep . 2019 Jun; 20:886-895. PMID: 31230060
BACKGROUND Systemic vasculitides constitute heterogenous conditions affecting many organs and systems through blood vessel inflammation. Although there are some classifications for vasculitis, several vasculitides are "unclassified" because they cannot be...
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Kaneko S, Watanabe E, Abe M, Watanabe S, Yabe H, Kojima S, et al.
J Med Case Rep . 2019 Mar; 13(1):74. PMID: 30890184
Background: Segmental arterial mediolysis is a rare nonarteriosclerotic and noninflammatory vascular disease that may cause intraperitoneal bleeding. Scleroderma renal crisis is a rare complication of systemic sclerosis, leading to severe...
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Watanabe S, Gono T, Nishina K, Sugitani N, Watanabe E, Yabe H, et al.
BMC Immunol . 2017 Dec; 18(1):53. PMID: 29262790
Background: Some patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) also have positivity of rheumatoid factor (RF). However, the clinical significance of this occurrence remains unknown in AAV patients. The...
8.
Hasegawa S, Yabe H, Kaneko N, Watanabe E, Gono T, Terai C
Intern Med . 2017 Sep; 56(20):2779-2783. PMID: 28924111
We herein report a rare case of a 66-year-old woman who had synovitis-acne-pustulosis-hyperostosis-osteitis (SAPHO) syndrome with marked sternal osteitis and bilateral pleural effusions. SAPHO syndrome was diagnosed based on the...
9.
Watanabe E, Sugawara H, Yamashita T, Ishii A, Oda A, Terai C
Case Rep Med . 2016 Oct; 2016:5656320. PMID: 27688774
We report the case of a 71-year-old Japanese woman with adult-onset Still's disease (AOSD) in whom macrophage activation syndrome (MAS) developed despite therapy with oral high-dose prednisolone and intravenous methylprednisolone...
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Migita K, Agematsu K, Yazaki M, Nonaka F, Nakamura A, Toma T, et al.
Medicine (Baltimore) . 2014 May; 93(3):158-164. PMID: 24797171
Familial Mediterranean fever (FMF) is an autoinflammatory disease caused by MEditerranean FeVer gene (MEFV) mutations. In Japan, patients with FMF have been previously reported, including a mild or incomplete form....