Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Kazushige Hanaoka"'
Autor:
Akinari Sekine, Sumi Hidaka, Tomofumi Moriyama, Yasuto Shikida, Keiji Shimazu, Eiji Ishikawa, Kiyotaka Uchiyama, Hiroshi Kataoka, Haruna Kawano, Mahiro Kurashige, Mai Sato, Tatsuya Suwabe, Shinya Nakatani, Tadashi Otsuka, Hirayasu Kai, Kan Katayama, Shiho Makabe, Shun Manabe, Wataru Shimabukuro, Koichi Nakanishi, Saori Nishio, Fumihiko Hattanda, Kazushige Hanaoka, Kenichiro Miura, Hiroki Hayashi, Junichi Hoshino, Ken Tsuchiya, Toshio Mochizuki, Shigeo Horie, Ichiei Narita, Satoru Muto
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 21, p 6528 (2022)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cystic kidney disease, with patients often having a positive family history that is characterized by a similar phenotype. However, in atypical cases, particularly thos
Externí odkaz:
https://doaj.org/article/f6f709b5fc3349d2bb527a1d4e5996b9
Autor:
Keiji Sugai, Hiroyuki Ueda, Keita Morimoto, Mai Tanaka, Daisuke Takahashi, Akio Nakashima, Junichiro Kato, Hiroshi Takahashi, Yutaka Yamaguchi, Tetsuya Kawamura, Kazushige Hanaoka, Yoichi Miyazaki, Takashi Yokoo
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Maternally inherited diabetes and deafness (MIDD), a mitochondrial genetic disorder, typically affects the kidneys and results in end-stage renal disease. Early diagnosis of MIDD is challenging when renal manifestations precede ot
Externí odkaz:
https://doaj.org/article/000fcae30b004f578642c5a278863222
Autor:
Mahiro Kurashige, Minako Imamura, Shin-Ichi Araki, Daisuke Suzuki, Tetsuya Babazono, Takashi Uzu, Tomoya Umezono, Masao Toyoda, Koichi Kawai, Masahito Imanishi, Kazushige Hanaoka, Hiroshi Maegawa, Yasuko Uchigata, Tatsuo Hosoya, Shiro Maeda
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54064 (2013)
BACKGROUND: Several linkage analyses have mapped a susceptibility locus for diabetic nephropathy to chromosome 18q22-23, and polymorphisms within the carnosine dipeptidase 1 gene (CNDP1), located on 18q22.3, have been shown to be associated with diab
Externí odkaz:
https://doaj.org/article/6f6a4bc4f48b48a6a0cb0e354d11e71d
Autor:
Tadashi Sofue, Akinari Sekine, Kazuhiko Tsuruya, Michihiro Mitobe, Toshio Mochizuki, Yosuke Shimada, Shigeo Horie, Shinya Nakatani, Ken Tsuchiya, Eiji Ishimura, Yoshifumi Ubara, Kazushige Hanaoka, Satoru Muto, Ichiei Narita, Satoshi Tanaka, Shoichi Maruyama, Hiroshi Kataoka, Kiyotaka Uchiyama, Kikuo Nutahara, Saori Nishio, Tatsuya Suwabe
Publikováno v:
Clinical and Experimental Nephrology. 25:970-980
Factors affecting decline in renal function and cyst growth in patients with autosomal polycystic kidney disease (ADPKD) are not fully described, particularly in Japan. This was the first multi-facility, prospective, observational cohort study conduc
Autor:
Ken Tsuchiya, Toshio Mochizuki, Masahiko Ando, Saori Nishio, Kazuhiko Tsuruya, Ichiei Narita, Satoru Muto, Shigeo Horie, Kouichi Kamura, Yoshifumi Ubara, Kazushige Hanaoka
Publikováno v:
Clinical and Experimental Nephrology. 24:314-322
Although it is widely accepted that the autosomal dominant polycystic kidney disease (ADPKD) patients with large liver cysts have a significant decrement in quality of life (QOL), there is insufficient evidence that clearly demonstrates the relations
Autor:
Kengo Furuichi, Kenichiro Miura, Keiji Shimazu, Hiroki Hayashi, Taketsugu Hama, Daisuke Ichikawa, Sumi Hidaka, Eiji Ishikawa, Soshiro Ogata, Koichi Seta, Kiyotaka Uchiyama, Kazushige Hanaoka, Eri Koshi-Ito, Shigeo Horie, Yoshikatsu Kaneko, Mahiro Kurashige, Shinya Nakatani, Ichiei Narita, Ken Tsuchiya, Shiho Makabe, Toshio Mochizuki, Hirayasu Kai, Hiroshi Kataoka, Akinari Sekine, Haruna Kawano, Hirokazu Okada, Satoru Muto, Koichi Nakanishi, Tatsuya Suwabe, Saori Nishio, Michihiro Mitobe
Publikováno v:
Clinical and experimental nephrology. 25(12)
Autor:
Kazushige Hanaoka, Harunobu Matsumoto, Takao Nonaka, Daijiro Hori, Koichi Yuri, Naoyuki Kimura, Mitsunori Nakano, Yusuke Sasabuchi, Keisuke Tanno, Atsushi Yamaguchi, Makiko Mieno, Yuichiro Kitada
Publikováno v:
Surgery today. 50(10)
We investigated the etiology and impact on outcomes of polycystic kidney disease in patients with abdominal aortic aneurysm. Eight-hundred patients who underwent open (n = 603) or endovascular aortic repair (n = 197) were divided into three groups: n
Autor:
Junichiro Kato, Yutaka Yamaguchi, Yoichi Miyazaki, Takashi Yokoo, Keiji Sugai, Tetsuya Kawamura, Hiroshi Takahashi, Keita Morimoto, Daisuke Takahashi, Akio Nakashima, Mai Tanaka, Hiroyuki Ueda, Kazushige Hanaoka
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-7 (2018)
BMC Nephrology
BMC Nephrology
Background Maternally inherited diabetes and deafness (MIDD), a mitochondrial genetic disorder, typically affects the kidneys and results in end-stage renal disease. Early diagnosis of MIDD is challenging when renal manifestations precede other key c
Autor:
Toshio Mochizuki, Yoshimitsu Fukushima, Koichi Nakanishi, Tatsuya Suwabe, Kikuo Nutahara, Kazuhiko Tsuruya, Satoru Muto, Koichi Kamura, Ken Tsuchiya, Shigeo Horie, Kenjiro Kimura, Eiji Ishimura, Saori Nishio, Seiichi Matsuo, Yoshifumi Ubara, Keiichi Furukawa, Kazushige Hanaoka, Ichiei Narita
Publikováno v:
Clinical and Experimental Nephrology. 20:493-509
ADPKD is the most common hereditary cystic kidney disease. ADPKD is characterized by the progressive development of fluid-filled cysts derived from renal tubular epithelial cells and the development of disorders in several organs. Bilateral renal cys
Autor:
Satoshi Endo, Kyoko Watanabe, Keita Hirano, Nobuo Tsuboi, Hoichi Amano, Masato Ikeda, Satoru Komatsumoto, Kazushige Hanaoka, Makoto Ogura, Akihiro Shimizu, Takashi Yokoo, Hideo Okonogi, Yoichi Miyazaki, Kentaro Koike, Tetsuya Kawamura
Publikováno v:
Clinical and Experimental Nephrology
Background In patients with IgA nephropathy (IgAN), recurrence after steroid pulse therapy is associated with reduced renal survival. However, the predictors of recurrence have not yet been clarified. Methods All patients who received 6-month steroid