Zobrazeno 1 - 10
of 207
pro vyhledávání: '"Tomohiro, Murata"'
Autor:
Ryosuke Saiki, Kan Katayama, Haruko Saiki, Ayumi Fukumori, Kayo Tsujimoto, Masahiro Yamawaki, Fumika Tanaka, Daisuke Takahashi, Keiko Oda, Yasuo Suzuki, Tomohiro Murata, Kaoru Dohi
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Recent studies have focused on immune checkpoint inhibitors. Renal complications associated with the use of immune checkpoint inhibitors are uncommon compared with other immune-related adverse events. Acute interstitial nephritis
Externí odkaz:
https://doaj.org/article/59291dfa7ab74ae6968c72831f86950e
Autor:
Shoko Miura, Kan Katayama, Yuka Sugimoto, Fumika Tanaka, Mutsuki Mori, Daisuke Takahashi, Ryosuke Saiki, Yosuke Hirabayashi, Tomohiro Murata, Isao Tawara, Kaoru Dohi
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background Proliferative glomerulonephritis with monoclonal immunoglobulin G (IgG) deposits (PGNMID) is a disease entity with nonorganized granular glomerular deposition with monoclonal proteins of both heavy and light chains. Dysproteinemia
Externí odkaz:
https://doaj.org/article/17e4b5d7b3c6470382a8f1c1c52dbdee
Autor:
Motohiro Maeda, Shun-Ichiro Sakamoto, Tomohiro Murata, Atsushi Hiromoto, Kenji Suzuki, Yosuke Ishii
Publikováno v:
Surgical Case Reports, Vol 9, Iss 1, Pp 1-5 (2023)
Abstract Background Essential thrombocythemia (ET) is a chronic myeloproliferative disorder characterized by an elevation of platelet counts with a tendency for thrombosis and hemorrhage. The perioperative management of cardiovascular surgery of an E
Externí odkaz:
https://doaj.org/article/75379a30d8134fea8c7a253776e9de79
Autor:
Keiko Oda, Kan Katayama, Liqing Zang, Masaaki Toda, Akiko Tanoue, Ryosuke Saiki, Taro Yasuma, Corina N. D’Alessandro-Gabazza, Yasuhito Shimada, Mutsuki Mori, Yasuo Suzuki, Tomohiro Murata, Toshinori Hirai, Karl Tryggvason, Esteban C. Gabazza, Kaoru Dohi
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 5808 (2024)
Approximately 30% of steroid-resistant nephrotic syndromes are attributed to monogenic disorders that involve 27 genes. Mutations in KANK family members have also been linked to nephrotic syndrome; however, the precise mechanism remains elusive. To i
Externí odkaz:
https://doaj.org/article/7f2e3c2855ab437f902c6114ae1c67d0
Autor:
Daisuke Takahashi, Kan Katayama, Yoshinobu Iyoda, Ayumi Fukumori, Kayo Tsujimoto, Masahiro Yamawaki, Fumika Tanaka, Ryosuke Saiki, Keiko Oda, Yasuo Suzuki, Tomohiro Murata, Yoshinaga Okugawa, Kaoru Dohi
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Most male X-linked Alport syndrome patients with COL4A5 nonsense mutations experience end-stage kidney failure by 30 years old. Although there is no definition of high-flow arteriovenous fistula, access blood flows greater than 2000 mL/min might pred
Externí odkaz:
https://doaj.org/article/94e7b2ef08554d22a75e841494502b91
Autor:
Ayumi Omori, Kan Katayama, Ryosuke Saiki, Satoru Masui, Kei Suzuki, Yoshinori Kanii, Kayo Tsujimoto, Shiro Nakamori, Tairo Kurita, Tomohiro Murata, Takahiro Inoue, Kaoru Dohi
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-7 (2022)
Abstract Background Nutcracker syndrome (NCS) is characterized by compression of the left renal vein (LRV) between the aorta and the superior mesenteric artery. While rare, NCS was reported to be accompanied by double inferior vena cava (IVC). We her
Externí odkaz:
https://doaj.org/article/72ef09b813b5441a9b426f4f70c7b769
Autor:
Ryosuke Saiki, Kan Katayama, Yosuke Hirabayashi, Keiko Oda, Mika Fujimoto, Tomohiro Murata, Ayako Nakajima, Kaoru Dohi
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background Multicentric Castleman’s disease is a life-threatening disorder involving a systemic inflammatory response and multiple organ failure caused by the overproduction of interleukin-6. Although renal complications of Castleman’s d
Externí odkaz:
https://doaj.org/article/01c73b9e96d045208ad6de8923fa2c7f
Autor:
Hiroshi Matsuo, Kan Katayama, Aoi Hayasaki, Yusuke Iizawa, Mayumi Endo, Tomohiro Murata, Shugo Mizuno, Kaoru Dohi
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent genetic kidney disease and polycystic liver disease is its major extrarenal manifestation, however biliary peritonitis due to a liver cyst rupture is extrem
Externí odkaz:
https://doaj.org/article/a732bea794704a9aae56854771cdcd79
Publikováno v:
Journal of Arrhythmia, Vol 38, Iss 1, Pp 163-165 (2022)
Externí odkaz:
https://doaj.org/article/a8072c5041944a41bc025e7069cd56b4
Autor:
Jingwen Song, Tomohiro Murata, Kun‐Che Tsai, Xiaofang Jia, Flavien Sciortino, Renzhi Ma, Yusuke Yamauchi, Jonathan P. Hill, Lok Kumar Shrestha, Katsuhiko Ariga
Publikováno v:
Advanced Materials Interfaces, Vol 9, Iss 11, Pp n/a-n/a (2022)
Abstract Ultrathin 2D nanoporous materials offer enhanced sensitivity and high spatial resolution in sensing applications making them important for the selective discrimination of guest molecules. Here bottom‐up fabrication is reported of a novel m
Externí odkaz:
https://doaj.org/article/05295652bd5641cca44221b4630818dc