Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Yohei Ikezumi"'
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-3 (2022)
Abstract Alport syndrome is a hereditary disorder characterized by renal impairment, hearing loss, and ocular symptoms and is caused by COL4A3, COL4A4, and COL4A5 mutations. Here, we report the case of 3-year-old boy with isolated hematuria detected
Externí odkaz:
https://doaj.org/article/59c3734fca294fc28699f1cef5a054a7
Autor:
Yuji Matsumoto, Yohei Ikezumi, Tomomi Kondo, Yoko Nakajima, Yasuto Yamamoto, Masashi Morooka, Satoru Kisohara, Tetsuya Ito, Tetsushi Yoshikawa
Publikováno v:
Fujita Medical Journal, Vol 4, Iss 1, Pp 17-22 (2018)
Objective: We previously reported that macrophages contribute to the pathogenesis of refractory nephrotic syndrome (NS). To elucidate the mechanism behind macrophage accumulation and to identify a predictive biomarker of steroid responsiveness, we co
Externí odkaz:
https://doaj.org/article/2c999dd64c2b4efca2dd1399172b0127
Autor:
Yuji Matsumoto, Yohei Ikezumi, Tomomi Kondoh, Katsuyuki Yokoi, Yoko Nakajima, Naonori Kumagai, Takema Kato, Hiroki Kurahashi, Tetsuya Ito
Publikováno v:
The Tohoku Journal of Experimental Medicine. 258:183-193
Autor:
Yohei Ikezumi
Publikováno v:
Japanese journal of pediatric nephrology. 35:71-78
Publikováno v:
The Tohoku Journal of Experimental Medicine. 257:73-76
Type 3 renal tubular acidosis is a pathological condition characterized by the simultaneous occurrence of distal renal tubular acidosis, which causes urinary acidification disorders, and proximal renal tubular acidosis, which causes impaired reabsorp
Autor:
Yohei Ikezumi, Masatoshi Yoshikane, Tomomi Kondoh, Yuji Matsumoto, Naonori Kumagai, Masahiro Kaneko, Hiroya Hasegawa, Takeshi Yamada, Toshiaki Suzuki, David J. Nikolic-Paterson
Publikováno v:
Pediatric nephrology (Berlin, Germany).
The immunosuppressant mizoribine (Miz) can reduce progression of childhood IgA nephropathy (IgAN). This study examined whether Miz affects CD163A retrospective cohort of 90 children with IgAN were divided into groups treated with prednisolone (PSL) a
Steroid treatment promotes an M2 anti-inflammatory macrophage phenotype in childhood lupus nephritis
Autor:
David J. Nikolic-Paterson, Yohei Ikezumi, Tomomi Kondoh, Naonori Kumagai, Yuji Matsumoto, Utako Kaneko, Hiroya Hasegawa, Takeshi Yamada, Masahiro Kaneko
Publikováno v:
Pediatric Nephrology. 36:349-359
M1-type proinflammatory macrophages (MΦ) promote glomerular injury in lupus nephritis (LN). However, whether this phenotype is altered by steroid therapy is unclear. Therefore, we investigated the effect of steroid treatment on MΦ phenotype in LN.
Autor:
Yuri Kawai, Tomomi Kondoh, Naoya Fujita, Yuji Matsumoto, Satoshi Hibino, Yohei Ikezumi, Masafumi Miyata, Naonori Kumagai, Kazuki Tanaka
Publikováno v:
The Tohoku Journal of Experimental Medicine. 252:9-14
Renal tubular dysgenesis (RTD) is the absence or poor development of the renal proximal tubules caused by gene mutations in the renin-angiotensin system. Although RTD has been considered fatal, improving neonatal intensive care management has enhance
Autor:
Yohei Ikezumi
Publikováno v:
Qeios.
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