Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Shigeru, Horita"'
Autor:
Taro Akihisa, Masayo Sato, Yoshie Wakayama, Sekiko Taneda, Shigeru Horita, Orie Hirose, Shiho Makabe, Hiroshi Kataoka, Takayasu Mori, Eisei Sohara, Shinichi Uchida, Kosaku Nitta, Toshio Mochizuki
Publikováno v:
Kidney Medicine, Vol 1, Iss 6, Pp 391-396 (2019)
Alport syndrome is a hereditary glomerular nephritis associated with hearing loss and eye abnormalities and is classified as X-linked Alport syndrome, autosomal recessive Alport syndrome, and autosomal dominant Alport syndrome. Autosomal dominant Alp
Externí odkaz:
https://doaj.org/article/abea7b16e4b544e69aee997d2b89705c
Autor:
Taeko Hashimoto, Yutaka Harita, Keiichi Takizawa, Seiya Urae, Kiyonobu Ishizuka, Kenichiro Miura, Shigeru Horita, Daisuke Ogino, Gen Tamiya, Hideki Ishida, Tetsuo Mitsui, Kiyoshi Hayasaka, Motoshi Hattori
Publikováno v:
Kidney International Reports, Vol 4, Iss 9, Pp 1312-1322 (2019)
Introduction: Mutations in genes encoding nucleoporins (NUPs; components of nuclear pore complexes [NPCs]), such as NUP93, have been reported to cause steroid-resistant nephrotic syndrome (SRNS) or focal segmental glomerulosclerosis (FSGS), which oft
Externí odkaz:
https://doaj.org/article/41e6a07eedce4ec9a065f923faba22bd
Autor:
Ai Katsuma, Yasuyuki Nakada, Izumi Yamamoto, Shigeru Horita, Miyuki Furusawa, Kohei Unagami, Haruki Katsumata, Masayoshi Okumi, Hideki Ishida, Takashi Yokoo, Kazunari Tanabe, Japan Academic Consortium of Kidney Transplantation (JACK)
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Patients with Alport syndrome (AS) develop progressive kidney dysfunction due to a hereditary type IV collagen deficiency. Survival of the kidney allograft in patients with AS is reportedly excellent because AS does not recur. How
Externí odkaz:
https://doaj.org/article/40a8918422c94d2a9645bef69b378b15
Autor:
Yoko Shirai, Kenichiro Miura, Takeshi Ike, Kensuke Sasaki, Kiyonobu Ishizuka, Shigeru Horita, Sekiko Taneda, Daishi Hirano, Kazuho Honda, Yutaka Yamaguchi, Takao Masaki, Motoshi Hattori
Publikováno v:
Kidney International Reports. 7:2431-2445
Neutral-pH dialysate has been reported to be beneficial to prevent the peritoneal pathological changes in adult peritoneal dialysis (PD) patients, but its use is controversial in pediatric PD patients. In addition, the impact of cumulative dialytic g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd34244619cc9ee8cae3fa712a944f8
https://doi.org/10.1016/j.ekir.2022.08.013
https://doi.org/10.1016/j.ekir.2022.08.013
Autor:
Yukiko, Kanetsuna, Kazunari, Tanabe, Motoshi, Hattori, Kosaku, Nitta, Takahito, Moriyama, Shigeru, Horita, Yutaka, Yamaguchi
Publikováno v:
International Urology and Nephrology. 54:2263-2273
Purpose Central fibrous areas (CFAs) are small, hyalinotic, monotonous nodular areas observed in glomerular vascular pole lesions. We attempted to clarify the relationship between CFA formation and age in healthy kidneys and in those affected by immu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acafb50e237aae9b89eb93c11eb4a324
https://doi.org/10.1007/s11255-022-03126-3
https://doi.org/10.1007/s11255-022-03126-3
Autor:
Junki Koike, Yoji Nagashima, Kazuho Honda, Akira Shimizu, Hideki Ishida, Kazunari Tanabe, Tomomi Tamura, Sekiko Taneda, Motoshi Hattori, Kosaku Nitta, Anri Sawada, Shigeru Horita, Masayoshi Okumi
Publikováno v:
Pathology International. 71:406-414
BackgroundMonoclonal tubular basement membrane immune deposits (TBMID) are identified by renal biopsy and are associated with progression of interstitial injury in renal allograft. However, the significance of TBMID in the native kidney remains uncle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a32f7ae96e5af7e4578a7d9dd54512
https://doi.org/10.1111/pin.13092
https://doi.org/10.1111/pin.13092
Autor:
Takashi Yokoyama, Makoto Toguchi, Junpei Iizuka, Shigeru Horita, Tsutomu Ishizuka, Yu Chu-Su, Yoji Nagashima, Toshio Takagi, Kazunari Tanabe, Yoshikazu Tokuoka
Publikováno v:
Photodiagnosis and photodynamic therapy. 40
Bladder cancer is a common malignant disease in developed countries. Early detection of malignancy is important using urine cytology. The 5-aminolevulinic acid (ALA)-based photodynamic diagnosis (ALA-PDD) has not been routinely applied in urine cytol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6970d2516a41dd23400389052e1fbb69
https://pubmed.ncbi.nlm.nih.gov/35998879
https://pubmed.ncbi.nlm.nih.gov/35998879
Autor:
Keiichi Takizawa, Naoto Kaneko, Tomoo Yabuuchi, Shigeru Horita, Sekiko Taneda, Kenichiro Miura, Yutaka Harita, Shoichiro Kanda, Yuko Akioka, Kazuho Honda, Motoshi Hattori, Kiyonobu Ishizuka
Publikováno v:
Clinical and Experimental Nephrology. 24:813-820
Renal hypoplasia (RH) is the most common cause of chronic kidney disease in children. In cases of RH, proteinuria is often induced by glomerular hypertrophy and hyperfiltration that is commonly associated with focal segmental glomerulosclerosis. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f04f3796af14e6402979a4582a41b962
https://doi.org/10.1007/s10157-020-01902-y
https://doi.org/10.1007/s10157-020-01902-y
Autor:
Kohei Unagami, Motoshi Hattori, Yutaka Yamaguchi, Naoto Kaneko, Hideki Ishida, Yoko Shirai, Junki Koike, Kazunari Tanabe, Miyuki Furusawa, Masayoshi Okumi, Shigeru Horita, Kiyonobu Ishizuka, Tomoo Yabuuchi, Kenichiro Miura, Kazuho Honda
Publikováno v:
Nephron. 144:97-101
Glomerular IgG deposition is rarely observed in antibody-mediated rejection. Here, we report chronic active antibody-mediated rejection with linear IgG deposition on glomerular capillary walls in a pediatric kidney transplant recipient. A 6-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36317fee3dc20e7d3f8db81b5717720e
https://doi.org/10.1159/000511322
https://doi.org/10.1159/000511322
Autor:
Yoshiaki Usui, Kosei Matsue, Kazuho Honda, Shota Ogura, Shigeru Horita, Hideaki Oda, Michihiro Mitobe, Sekiko Taneda, Kosaku Nitta
Publikováno v:
Kidney International Reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02f8183acdfc3e01939e5150cfaccc32
https://doi.org/10.1016/j.ekir.2019.09.012
https://doi.org/10.1016/j.ekir.2019.09.012