Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Ashio YOSHIMURA"'
Autor:
Reiji Takami, Yoshikuni Nagayama, Hiroki Nishiwaki, Toshiharu Ueno, Shigeki Iwasaki, Ashio Yoshimura, Fumihiko Koiwa
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 158-163 (2024)
Introduction: Malakoplakia is a rare and chronic granulomatous disease that is pathologically characterized by the presence of Michaelis-Gutmann bodies and large macrophage clusters. Malakoplakia of the renal parenchyma is especially rare. In this re
Externí odkaz:
https://doaj.org/article/32bc9c5005c045f6aca601fc4635d47f
Publikováno v:
Kidney Medicine, Vol 6, Iss 11, Pp 100896- (2024)
Rationale & Objective: Allopurinol and febuxostat, which are xanthine oxidoreductase inhibitors, have been widely used as uric acid-lowering medications. However, evidence regarding their cardiovascular effects in hemodialysis is insufficient. This s
Externí odkaz:
https://doaj.org/article/339cbec8a00740ddb01c5984b332a710
Autor:
Yoshinori Sato, Hiroyasu Tsukaguchi, Koichiro Higasa, Naoto Kawata, Kiyoko Inui, Tran Nguyen Truc Linh, Tran Thuy Huong Quynh, Inoue Yoshihiko, Fumihiko Koiwa, Ashio Yoshimura
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Although most IgAN cases are sporadic, few show a familial aggregation. However, the prevalence and prognosis of IgAN individuals with positive famili
Externí odkaz:
https://doaj.org/article/4d51439a482d4421a2539bb4365973b0
Autor:
Federica Piani, Fumihiko Sasai, Petter Bjornstad, Claudio Borghi, Ashio Yoshimura, Laura G. Sanchez-Lozada, Carlos Roncal-Jimenez, Gabriela E. Garcia, Ana Andres Hernando, Gabriel Cara Fuentes, Bernardo Rodriguez-Iturbe, Miguel A Lanaspa, Richard J Johnson
Publikováno v:
Brazilian Journal of Nephrology, Vol 43, Iss 4, Pp 572-579 (2021)
Abstract Hyperuricemia is common in chronic kidney disease (CKD) and may be present in 50% of patients presenting for dialysis. Hyperuricemia can be secondary to impaired glomerular filtration rate (GFR) that occurs in CKD. However, hyperuricemia can
Externí odkaz:
https://doaj.org/article/17dc9e9c3b2f4e41a45a0c534b40d10d
Publikováno v:
Kidney & Blood Pressure Research, Vol 37, Iss 6, Pp 557-566 (2013)
Background/Aims: Prolonged elevation of serum aldosterone leads to renal fibrosis. Inflammation also plays a role in the pathogenesis of renal disease. We used a rat model of interstitial renal fibrosis to test the hypothesis that eplerenone-mediated
Externí odkaz:
https://doaj.org/article/cd22635a6fcb483da11c851af694568f
Autor:
Haruhisa Otani, Tadashi Okada, Yasushi Saika, Michiko Sakagashira, Hiroaki Oda, Yoshiaki Ito, Takashi Yasuda, Takeo Kanno, Miyuki Shimazui, Shoko Yamao, Yoshie Kanazawa, Machiko Shimode, Mami Otani, Shinichiro Ueda, Toshiyuki Nakao, Ashio Yoshimura
Publikováno v:
Journal of Renal Nutrition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e571bdd2400a3b2462def1f7c8891499
https://doi.org/10.1053/j.jrn.2023.05.001
https://doi.org/10.1053/j.jrn.2023.05.001
Autor:
Naoto Kawata, Fumihiko Koiwa, Tran Thuy Huong Quynh, Tran Nguyen Truc Linh, Yoshinori Sato, Koichiro Higasa, Hiroyasu Tsukaguchi, Ashio Yoshimura, Inoue Yoshihiko, Kiyoko Inui
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-10 (2021)
BMC Nephrology
BMC Nephrology
Background IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Although most IgAN cases are sporadic, few show a familial aggregation. However, the prevalence and prognosis of IgAN individuals with positive familial histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3113cd82a40cd8647e077aa0981e5a4f
https://doaj.org/article/4d51439a482d4421a2539bb4365973b0
https://doaj.org/article/4d51439a482d4421a2539bb4365973b0
Autor:
Carlos A. Roncal-Jimenez, Claudio Borghi, Ashio Yoshimura, Fumihiko Sasai, Ana Andres Hernando, Gabriela E. Garcia, Richard J. Johnson, Bernardo Rodriguez-Iturbe, Laura G. Sánchez-Lozada, Miguel A. Lanaspa, Gabriel Cara Fuentes, Federica Piani, Petter Bjornstad
Publikováno v:
Brazilian Journal of Nephrology v.43 n.4 2021
Jornal Brasileiro de Nefrologia
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Brazilian Journal of Nephrology, Vol 43, Iss 4, Pp 572-579 (2021)
Jornal Brasileiro de Nefrologia
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Brazilian Journal of Nephrology, Vol 43, Iss 4, Pp 572-579 (2021)
Hyperuricemia is common in chronic kidney disease (CKD) and may be present in 50% of patients presenting for dialysis. Hyperuricemia can be secondary to impaired glomerular filtration rate (GFR) that occurs in CKD. However, hyperuricemia can also pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ca2cda1ddd7d0e48a38b0d11d3c037
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400572
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400572
Autor:
Keigyou Yoh, Ryusuke Koshida, Masafumi Muratani, Hyojung Jeon, Takaaki Ojima, Yuki Imamura, Michito Hamada, Naoki Morito, Maho Kanai, Hideki Yokoi, Manoj Kumar Yadav, Satoru Takahashi, Ashio Yoshimura, Hisashi Oishi, Masato Kasahara, Toshiaki Usui, Keigo Asano, Hossam H. Shawki, Joichi Usui, Yoshinori Sato, Akihiro Kuno, Takashi Kudo, Yuki Tsunakawa, Kunihiro Yamagata, Risa Okada, Hiroyasu Tsukaguchi
Publikováno v:
Kidney International. 98:391-403
Focal segmental glomerulosclerosis (FSGS) is a common cause of steroid-resistant nephrotic syndrome. Spontaneous remission of FSGS is rare and steroid-resistant FSGS frequently progresses to renal failure. Many inheritable forms of FSGS have been des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe048f78149d2fb70611172351ea0ce5
https://doi.org/10.1016/j.kint.2020.02.038
https://doi.org/10.1016/j.kint.2020.02.038
Autor:
Hiroyasu Tsukaguchi, Izumi Yamaguchi, Toshiaki Usui, Ashio Yoshimura, Hiroyuki Morita, Takao Hayashi, Naoki Morito, Mai Thi Nhu Tran, Hiroshi Sato, Huan Thanh Nguyen, Yoshinori Sato, Yuichi Maruta, Fumihiko Koiwa, Masayo Harada, Fumihiko Matsuda, Junko Takagi, Satoru Takahashi, Shinya Ayabe, Yoshihiko Inoue, Seiya Mizuno, Michito Hamada, Koichiro Higasa, Shoichiro Horita, Kiyoko Inui, Fumihiro Sugiyama
Publikováno v:
Kidney International. 94:396-407
Focal segmental glomerulosclerosis (FSGS) is a leading cause of end-stage renal disease in children and adults. Genetic factors significantly contribute to early-onset FSGS, but the etiologies of most adult cases remain unknown. Genetic studies of mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::029daf451cb1696b452b8e9ebea4541e
https://doi.org/10.1016/j.kint.2018.02.025
https://doi.org/10.1016/j.kint.2018.02.025