H
Hitoshi Ogawa
Researcher at St. Marianna University School of Medicine
Publications - 4
Citations - 157
Hitoshi Ogawa is an academic researcher from St. Marianna University School of Medicine. The author has contributed to research in topics: Dermatomyositis & Anti-neutrophil cytoplasmic antibody. The author has an hindex of 4, co-authored 4 publications receiving 133 citations.
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Journal ArticleDOI
Longterm survival and associated risk factors in patients with adult-onset idiopathic inflammatory myopathies and amyopathic dermatomyositis: experience in a single institute in Japan.
Yoshioki Yamasaki,Hidehiro Yamada,Michiko Ohkubo,Masaomi Yamasaki,Kohei Azuma,Hitoshi Ogawa,Machiko Mizushima,Shoichi Ozaki +7 more
TL;DR: Survival of clinically ADM and primary DM was low, mainly due to fatal ILD, compared to primary PM, and establishing therapeutic strategy for ILD may improve the survival in the patient population.
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Clinical subsets associated with different anti-aminoacyl transfer RNA synthetase antibodies and their association with coexisting anti-Ro52.
Yoshioki Yamasaki,Minoru Satoh,Minoru Satoh,Machiko Mizushima,Takahiro Okazaki,Hiroko Nagafuchi,Seido Ooka,Tomohiko Shibata,Hiromasa Nakano,Hitoshi Ogawa,Kohei Azuma,Akihiko Maeda,Kumiko Tonooka,Hiroshi Ito,Yukiko Takakuwa,Makoto Inoue,Hirofumi Mitomi,Tomofumi Kiyokawa,Kosei Tsuchida,Hiromi Matsushita,Hidenori Mikage,Yoshihiko Murakami,Jason Y F Chan,Shoichi Ozaki,Hidehiro Yamada +24 more
TL;DR: Patients with different anti-ARS in combination with anti-Ro52 appear to be associated with distinctive clinical subsets.
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Cutaneous manifestations in patients with microscopic polyangiitis: two case reports and a minireview.
Tamihiro Kawakami,Yoshinao Soma,Chihiro Saito,Hitoshi Ogawa,Yuko Nagahuchi,Takahiro Okazaki,Shoichi Ozaki,Masako Mizoguchi +7 more
TL;DR: The initial cutaneous manifestations of microscopic polyangiitis are important in early diagnosis of possible ANCA-associated vasculitides with elevated ANCA titres.
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Cutaneous polyarteritis nodosa associated with HLA-B39-positive undifferentiated spondyloarthritis in a Japanese patient
Hiromasa Nakano,Seido Ooka,Tomohiko Shibata,Hitoshi Ogawa,Hiroshi Ito,Yukiko Takakuwa,Kumiko Tonooka,Akihiko Maeda,Yoshioki Yamasaki,Tomofumi Kiyokawa,Hiroko Nagafuchi,Hidehiro Yamada,Shoichi Ozaki +12 more
TL;DR: The case of a 43-year-old man diagnosed with HLA-B39-positive spondyloarthritis who developed cutaneous lesions consistent with cutaneous polyarteritis nodosa (CPN) was presented, suggesting that CPN may also occur in association with forms of HLA.