Zobrazeno 1 - 10
of 274
pro vyhledávání: '"Norishige Yoshikawa"'
Autor:
Shingo Ishimori, Takashi Ando, Kaori Kikunaga, Chikako Terano, Mai Sato, Fumiyo Komaki, Riku Hamada, Yuko Hamasaki, Yoshinori Araki, Yoshimitsu Gotoh, Koichi Nakanishi, Hitoshi Nakazato, Takeshi Matsuyama, Kazumoto Iijima, Norishige Yoshikawa, Shuichi Ito, Masataka Honda, Kenji Ishikura
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Although vaccination may precipitate relapses of nephrotic syndrome (NS) in children with idiopathic NS, no data are available regarding NS activity regarding influenza (flu) virus infections and NS relapses after receiving inactivated flu v
Externí odkaz:
https://doaj.org/article/93d0413275084672b3fb9346a98b2166
Autor:
Chikako Terano, Riku Hamada, Ichiro Tatsuno, Yuko Hamasaki, Yoshinori Araki, Yoshimitsu Gotoh, Koichi Nakanishi, Hitoshi Nakazato, Takeshi Matsuyama, Kazumoto Iijima, Norishige Yoshikawa, Tetsuji Kaneko, Shuichi Ito, Masataka Honda, Kenji Ishikura, Japanese Study Group of Renal Disease in Children
Publikováno v:
PLoS ONE, Vol 17, Iss 7, p e0270796 (2022)
BackgroundLittle is known about the epidemiology of Henoch-Schönlein purpura nephritis (HSPN).MethodsWe conducted a nationwide epidemiological survey of Japanese children aged 1 to 15 years with HSPN. Children who were newly diagnosed with HSPN by b
Externí odkaz:
https://doaj.org/article/3a5d6cb3a97449a380605ab7549013c8
Autor:
Shinya Ishiko, Tomoko Horinouchi, Rika Fujimaru, Yuko Shima, Hiroshi Kaito, Ryojiro Tanaka, Shingo Ishimori, Atsushi Kondo, Sadayuki Nagai, Yuya Aoto, Nana Sakakibara, China Nagano, Tomohiko Yamamura, Momoka Yoshimura, Koichi Nakanishi, Junya Fujimura, Naohiro Kamiyoshi, Hiroaki Nagase, Norishige Yoshikawa, Kazumoto Iijima, Kandai Nozu
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-6 (2020)
Abstract Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with neph
Externí odkaz:
https://doaj.org/article/51582829b5bb434c960fdaccff19cb9f
Autor:
Taketsugu Hama, Koichi Nakanishi, Kenji Ishikura, Shuichi Ito, Hidefumi Nakamura, Mayumi Sako, Mari Saito-Oba, Kandai Nozu, Yuko Shima, Kazumoto Iijima, Norishige Yoshikawa, for the Japanese Study Group of Kidney Disease in Children (JSKDC)
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Eighty percent of children with steroid-sensitive nephrotic syndrome (SSNS) relapse within 2 years and 40–50% patients show frequently-relapsing nephrotic syndrome (FRNS). Patients showing a relapse within 6 months after initial
Externí odkaz:
https://doaj.org/article/4f3b0ea7b8a642b885add50815a7f2e5
Autor:
Hiroshi Yamaguchi, Atsutoshi Shiratori, Taku Nakagawa, Kyoko Kanda, Shigeo Hara, Norishige Yoshikawa, Ryojiro Tanaka
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 7, Iss 3, Pp 161-166 (2017)
The underlying histopathology is very important in determining patient management, as the histopathology usually has direct repercussions on the treatment response and clinical course. However, the impact of the method used to assess renal biopsies,
Externí odkaz:
https://doaj.org/article/cff4d18c6b1f43d6b92667833abb302b
Autor:
Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, Yoshimi Nozu, Ming Juan Ye, Akemi Shono, Satoko Yamanouchi, Shogo Minamikawa, Naoya Morisada, Koichi Nakanishi, Yuko Shima, Norishige Yoshikawa, Takeshi Ninchoji, Ichiro Morioka, Hiroshi Kaito, Kazumoto Iijima
Publikováno v:
Kidney International Reports, Vol 2, Iss 5, Pp 850-855 (2017)
X-linked Alport syndrome (XLAS) is a hereditary disease characterized by progressive nephritis, hearing loss, and ocular abnormalities. Affected male patients usually progress to end-stage renal disease in early or middle adulthood, and disease sever
Externí odkaz:
https://doaj.org/article/0f24d6986d3a415a8d43c8725ee61bbc
Publikováno v:
International Journal of Inflammation, Vol 2012 (2012)
Infection with Shiga toxin- (Stx-) producing Escherichia coli can lead to hemolytic uremic syndrome (HUS). Approximately, 30% of patients with HUS suffer from complications in the central nervous system (CNS), which is an important determinant of mor
Externí odkaz:
https://doaj.org/article/f6395aa890a444829b59199d0b97e742
Autor:
Hideaki Kitakado, Tomoko Horinouchi, Chika Masuda, Atsushi Kondo, Sadayuki Nagai, Yuya Aoto, Nana Sakakibara, Takeshi Ninchoji, Norishige Yoshikawa, Kandai Nozu
Publikováno v:
Pediatric Nephrology. 38:757-762
Oligomeganephronia (OMN) is a rare congenital anomaly involving the kidney and urinary tract, characterized by decreased number and compensatory hypertrophy of the nephron. It is caused by abnormal kidney development during the embryonic period, espe
Autor:
Yuta Ichikawa, Tomoko Horinouchi, Yu Tanaka, Chika Ueda, Hideaki Kitakado, Atsushi Kondo, Nana Sakakibara, Norishige Yoshikawa, Kandai Nozu
Publikováno v:
CEN Case Reports.
Autor:
Yuya Aoto, Takeshi Ninchoji, Hiroshi Kaito, Yuko Shima, Junya Fujimura, Naohiro Kamiyoshi, Shingo Ishimori, Koichi Nakanishi, Shogo Minamikawa, Shinya Ishiko, Nana Sakakibara, China Nagano, Tomoko Horinouchi, Tomohiko Yamamura, Sadayuki Nagai, Atsushi Kondo, Yosuke Inaguma, Ryojiro Tanaka, Norishige Yoshikawa, Kazumoto Iijima, Kandai Nozu
Publikováno v:
Clinical and Experimental Nephrology. 26(6):561-570
Background Patients with immunoglobulin A nephropathy who present with focal mesangial proliferation (focal IgAN) can have a relatively good prognosis, and renin-angiotensin system inhibitor (RAS-i) is commonly used as the initial treatment. However,