Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Naofumi Imai"'
Autor:
Hirofumi Watanabe, Shin Goto, Michihiro Hosojima, Hideyuki Kabasawa, Naofumi Imai, Yumi Ito, Ichiei Narita
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-3 (2023)
Abstract We present a family of two female Alport syndrome patients with a family history of impaired glucose tolerance. Whole exome sequencing identified a novel heterozygous variant of COL4A5 NM_033380.3: c.2636 C > A (p.S879*) and a rare variant o
Externí odkaz:
https://doaj.org/article/c3a5b6b3fd0143cabf5a829288d4b5c0
Autor:
Takako Saeki, Takashi Kuroha, Yuya Sato, Maasa Tamura, Akira Iguchi, Tomoyuki Ito, Hajime Yamazaki, Yumi Ito, Kazuhiro Yoshita, Naofumi Imai, Ichiei Narita, Hiroyuki Usuda
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Although most cases of tubulointerstitial nephritis in paraproteinemia are monoclonal light chain deposition-mediated, interstitial nephritis as neoplastic interstitial cell infiltration has rarely been described. On the other han
Externí odkaz:
https://doaj.org/article/7e939b55b135437e8a9a6d898d225d68
Autor:
Masanori Sudo, Takuya Wakamatsu, Tomomi Ishikawa, Masato Habuka, Michihiro Hosojima, Suguru Yamamoto, Yumi Ito, Naofumi Imai, Yoshikatsu Kaneko, Akira Shimizu, Ichiei Narita
Publikováno v:
Human Pathology: Case Reports, Vol 15, Iss , Pp 99-104 (2019)
Heavy chain deposition disease (HCDD) is a rare complication of plasma cell dyscrasias, characterized by nonamyloid tissue deposits of incomplete monoclonal heavy chains in renal tissues. We report the case of a 78-year-old female with HCDD who was s
Externí odkaz:
https://doaj.org/article/2f26174e64494d469b1a164bbe277214
Autor:
Masanori Sudo, Yuichi Sakamaki, Michihiro Hosojima, Suguru Yamamoto, Yumi Ito, Naofumi Imai, Yoshikatsu Kaneko, Shin Goto, Chih-Ping Li, Akira Shimizu, Ichiei Narita
Publikováno v:
Human Pathology: Case Reports, Vol 15, Iss , Pp 83-87 (2019)
A 60-year-old male presented with accelerated hypertension, renal insufficiency, proteinuria, and hematuria. Percutaneous kidney biopsy revealed membranoproliferative glomerulonephritis (MPGN) without any immunoglobulin and complement deposition. On
Externí odkaz:
https://doaj.org/article/194cfa13c40d4001a749dd5e3bbb9f65
Autor:
Ryo Koda, Hirofumi Watanabe, Masafumi Tsuchida, Noriaki Iino, Kazuo Suzuki, Go Hasegawa, Naofumi Imai, Ichiei Narita
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Acute tubulointerstitial nephritis (ATIN) has been increasingly recognized as an important manifestation of kidney injury associated with the use of immune checkpoint inhibitors (anti-PD-1 and anti-CTLA-4). While the exact pathoph
Externí odkaz:
https://doaj.org/article/79d619578bca453ba5299d8b6ed88fba
Autor:
Honami Mori, Shinichi Nishi, Mitsuhiro Ueno, Naofumi Imai, Susumu Ookawara, Yoshiyuki Mirishita, Ichiei Narita, Kaoru Tabei
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 27, Iss 5, Pp 885-892 (2016)
We detected an increase in small arterioles around glomeruli, particularly adjacent to tuft adhesive lesions in immunoglobulin A nephropathy (IgAN), for the 1 st time, as far as we know. We labeled these as periglomerular microarterioles (PGMAs). Thi
Externí odkaz:
https://doaj.org/article/08b6f7d3616f4618992be106855392b4
Autor:
Mitsuhiro Kawano, Ichiro Mizushima, Yutaka Yamaguchi, Naofumi Imai, Hitoshi Nakashima, Shinichi Nishi, Satoshi Hisano, Nobuaki Yamanaka, Motohisa Yamamoto, Hiroki Takahashi, Hisanori Umehara, Takao Saito, Takako Saeki
Publikováno v:
International Journal of Rheumatology, Vol 2012 (2012)
Although tubulointerstitial nephritis with IgG4+ plasma cell (PC) infiltration is a hallmark of IgG4-related kidney disease (IgG4-RKD), only a few studies are available about the minimum number of IgG4+ PC needed for diagnosis along with IgG4+/IgG+ P
Externí odkaz:
https://doaj.org/article/6bc492996d1b498d976dbb0530252f50
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 11, p1615-1621, 7p
Autor:
Ichiei Narita, Naofumi Imai, Kota Takahashi, Yutaka Yoshida, Masayuki Tasaki, Yuki Nakagawa, Shoko Ishikawa, Kazuhide Saito, Yoshihiko Tomita, Yumi Ito, Masahiro Ikeda
Publikováno v:
International Journal of Urology. 26:1128-1137
OBJECTIVES To analyze the prevalence of systemic de novo thrombotic microangiopathy in ABO-incompatible kidney transplantation and risk factors associated with this condition. METHODS A total of 201 patients who received living-donor kidney transplan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f681a2cdf90e8f6267e27b98b9a90971
https://doi.org/10.1111/iju.14118
https://doi.org/10.1111/iju.14118
Autor:
Kohei Miura, Takashi Kobayashi, Masanori Sudo, Yumi Ito, Takeshi Yamada, Masahiro Ikeda, Kazuhide Saito, Hiroya Hasegawa, Kota Takahashi, Ichie Narita, Naofumi Imai, Masayuki Tasaki, Yohei Ikezumi, Yoshihiko Tomita, Yuki Nakagawa
Publikováno v:
Transplantation Proceedings. 51:1732-1738
Plasma cell-rich acute rejection (PCAR) and antibody-mediated rejection (ABMR), for which a standard treatment has not yet been established, are associated with poor graft survival after kidney transplantation. Here, we report a case series of 3 Japa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71f8854b7e9b834f08317c847b919a9c
https://doi.org/10.1016/j.transproceed.2019.02.038
https://doi.org/10.1016/j.transproceed.2019.02.038