Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fae Suzuki"'
Autor:
Hideki Nomura, Kazuyuki Suzuki, Takeshi Zoshima, Mitsuhiro Kawano, Fae Suzuki, Ichiro Mizushima, Hiroshi Fujii, Keishi Mizuguchi, Kiyoaki Ito, Satoshi Hara
Publikováno v:
Clinical and experimental nephrology. 24(11)
Although crescentic glomerulonephritis is a hallmark of ANCA-associated nephritis, the clinicopathological features of ANCA-associated nephritis without crescent formation remain to be elucidated. We enrolled 146 Japanese ANCA-associated vasculitis (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dce2fee304e6ae24300e485c2cfb5fc
https://pubmed.ncbi.nlm.nih.gov/32651749
https://pubmed.ncbi.nlm.nih.gov/32651749
Autor:
Hiroshi Fujii, Mitsuhiro Kawano, Y. Fujisawa, Ichiro Mizushima, S Tsuge, Satoshi Hara, Kiyoaki Ito, Kazunori Yamada, Fae Suzuki
Publikováno v:
Rheumatology.
Objectives In IgG4-related disease (IgG4-RD), relapse including recurrent organ involvement (ROI) and de novo organ involvement (DNOI) occurs frequently during the clinical course. This study aimed to clarify the differences between the risk factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd0d20d0e5b9f8c3b1e3738a59126b3
https://doi.org/10.1093/rheumatology/kez321
https://doi.org/10.1093/rheumatology/kez321
Publikováno v:
Poster Presentations.
Background: The most typical histopathological feature of ANCA-associated glomerulonephritis (ANCA-GN) is crescentic GN. However, ANCA-GN is also complicated by other renal lesions, including vascular ones (arteritis and arteriolitis) and tubulointer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca6706964d1aabf7363031cae1d591e
https://doi.org/10.1136/annrheumdis-2019-eular.4486
https://doi.org/10.1136/annrheumdis-2019-eular.4486
Autor:
Fae Suzuki, Mitsuhiro Kawano, S Tsuge, Kazunori Yamada, Y. Fujisawa, Satoshi Hara, Hiroshi Fujii, Ichiro Mizushima, Kiyoaki Ito
Publikováno v:
Poster Presentations.
Background IgG4-related disease (IgG4-RD) is a recently recognized systemic inflammatory disorder that can affect many organs [1]. In IgG4-RD, relapse including recurrence of existing organ involvement (REOI) and new development of organ involvement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df10ea0ee4ad4d93c23890e82ab67956
https://doi.org/10.1136/annrheumdis-2017-eular.2425
https://doi.org/10.1136/annrheumdis-2017-eular.2425
Autor:
Ichiro Mizushima, Hiroshi Fujii, S Tsuge, Mitsuhiro Kawano, Y. Fujisawa, Fae Suzuki, Kazunori Yamada, Satoshi Hara, Kiyoaki Ito
Publikováno v:
Poster Presentations.
Background Immunoglobulin G4-related disease (IgG4-RD) is a recently recognized systemic inflammatory disease with multi-organ involvement [1]. Diagnostically, two of the most important hallmarks of IgG4-RD are high IgG4-positive plasma cell (PC) cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16356baf6533f6b18a9520658ee7c75a
https://doi.org/10.1136/annrheumdis-2017-eular.4170
https://doi.org/10.1136/annrheumdis-2017-eular.4170
Autor:
Kazunori Yamada, Kiyoaki Ito, Ichiro Mizushima, Mitsuhiro Kawano, Y. Fujisawa, Fae Suzuki, Satoshi Hara, S Tsuge, H. Fuji
Publikováno v:
Poster Presentations.
Background IgG4-related kidney disease (IgG4-RKD) is a comprehensive term for renal lesions associated with IgG4-related disease [1]. IgG4-RKD is frequently complicated by hypocomplementemia [1, 2, 3], but its clinical significance and mechanisms hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a938fc61af1378c390e2143b3f4a117
https://doi.org/10.1136/annrheumdis-2017-eular.4257
https://doi.org/10.1136/annrheumdis-2017-eular.4257