Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Kiho, Tanaka"'
Autor:
Tatsuya Suwabe, MD, MSc, PhD, Yoshifumi Ubara, MD, PhD, Yuki Oba, MD, Hiroki Mizuno, MD, Daisuke Ikuma, MD, PhD, Masayuki Yamanouchi, MD, MPH, PhD, Akinari Sekine, MD, Kiho Tanaka, MD, Eiko Hasegawa, MD, Junichi Hoshino, MD, MPH, PhD, Naoki Sawa, MD
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 7, Iss 1, Pp 69-80 (2023)
Objective: To examine the changes in total kidney volume (TKV) and total liver volume (TLV) before and after dialysis initiation in patients with autosomal dominant polycystic kidney disease. Patients and Methods: This was a retrospective, single-cen
Externí odkaz:
https://doaj.org/article/56faa27fca6249fbad4b16cd63d68027
Autor:
Kanako Terakawa, Akinari Sekine, Noriko Inoue, Yuki Oba, Hiroki Mizuno, Daisuke Ikuma, Kiho Tanaka, Masayuki Yamanouchi, Eiko Hasegawa, Tatsuya Suwabe, Shinji Urakami, Naoki Sawa, Yoshifumi Ubara, Junichi Hoshino
Publikováno v:
Internal Medicine. 62:1625-1629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d12d7b5b71a44a3298c3f32a24a15bc5
https://doi.org/10.2169/internalmedicine.0305-22
https://doi.org/10.2169/internalmedicine.0305-22
Publikováno v:
Renal Replacement Therapy, Vol 5, Iss 1, Pp 1-5 (2019)
Abstract Background Generally, the preferred route of vascular access in chronic kidney disease patients is an arteriovenous fistula (AVF) rather than grafts. However, approximately 7% of 300,000 Japanese hemodialysis (HD) patients continue to dialyz
Externí odkaz:
https://doaj.org/article/9f50353e91054d4480143f1fedb16cb1
Autor:
Masatoshi Matsunami, Kazuya Kinoshita, Kiho Tanaka, Yuki Nakamura, Kenichi Ohashi, Takeshi Fujii, Yoshifumi Ubara, Yasuo Ishii
Publikováno v:
Renal Replacement Therapy, Vol 5, Iss 1, Pp 1-5 (2019)
Abstract Background Cystinuria is a rare autosomal recessive metabolic disorder that affects renal and intestinal cystine transport. Cystine stones are found in only 1–2% of all stone formers. Patients with cystinuria are at high risk for nephrolit
Externí odkaz:
https://doaj.org/article/c15ae348910f4028ab4737cb8116fc4e
Autor:
Risa Hara, Eiko Hasegawa, Noriko Inoue, Akinari Sekine, Kiho Tanaka, Daisuke Ikuma, Hiroki Mizuno, Yuki Oba, Masayuki Yamanouchi, Tatsuya Suwabe, Naoki Sawa, Kei Kono, Keiichi Kinowaki, Kenichi Ohashi, Yoshifumi Ubara, Junichi Hoshino
Publikováno v:
Internal Medicine. 62:1077-1080
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8debe926b071b7f56fbd5fd391ed1ac
https://doi.org/10.2169/internalmedicine.9410-22
https://doi.org/10.2169/internalmedicine.9410-22
Publikováno v:
Viruses, Vol 14, Iss 5, p 1108 (2022)
Three early-career female virologists sat down with a distinguished Nobel laureate to discuss two pandemics, 39 years apart [...]
Externí odkaz:
https://doaj.org/article/f2e312901f3148018ba1d7a640bc2de9
Autor:
Kiho, Tanaka
Publikováno v:
同志社大学教職課程年報 = The annual bulletin of the Teacher-Training Course at Doshisha University. 12:46-56
非対面授業経験学生を対象に、対面授業に対する認知を調査し、大学における授業形態に関する今後の課題について検討することを目的とした。対面授業の「メリット」として、内容を
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::c61bfb3ba556b5927bd445497839da14
http://id.nii.ac.jp/1707/00029650/
http://id.nii.ac.jp/1707/00029650/
Autor:
Tatsuya Suwabe, Yoshifumi Ubara, Yuki Oba, Hiroki Mizuno, Daisuke Ikuma, Masayuki Yamanouchi, Akinari Sekine, Kiho Tanaka, Eiko Hasegawa, Junichi Hoshino, Naoki Sawa
Publikováno v:
Journal of Nephrology. 36:999-1010
Renal cyst bleeding is a frequent problem in patients with autosomal dominant polycystic kidney disease (ADPKD). However, there remains minimal information concerning its frequency, causative factors, and effects on ADPKD progression. We investigated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68cf87ba19142b8acddaa4b96d92758
https://doi.org/10.1007/s40620-022-01562-z
https://doi.org/10.1007/s40620-022-01562-z
Publikováno v:
Transplantation Reports, Vol 5, Iss 3, Pp 100047- (2020)
Background: The use of laparoscopy is increasing in various surgical disciplines, including living donor kidney transplant (LDKT). In laparoscopic transplants, vessel length of the donor kidneys often falls short. This makes anastomosis to the recipi
Externí odkaz:
https://doaj.org/article/13c2fc7438264794a9833a709b4d79ad
Autor:
Masatoshi Matsunami, Yoshifumi Ubara, Keiichi Sumida, Yoichi Oshima, Masahiko Oguro, Kazuya Kinoshita, Kiho Tanaka, Yuki Nakamura, Keiichi Kinowaki, Kenichi Ohashi, Takeshi Fujii, Takuro Igawa, Yasuharu Sato, Yasuo Ishii
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Multicentric Castleman disease (MCD) is an uncommon lymphoproliferative disease characterized by systemic inflammatory reactions associated with the dysregulated production of interleukin-6 (IL-6). In patients with MCD, renal invo
Externí odkaz:
https://doaj.org/article/51c90ee776f841cb8944814ecc4c4ec0