Zobrazeno 1 - 10
of 230
pro vyhledávání: '"EIJI HIGASHIHARA"'
Autor:
Eiji Higashihara, Kikuo Nutahara, Masayuki Itoh, Takatsugu Okegawa, Mistuhiro Tambo, Tsuyoshi Yamaguchi, Yu Nakamura, Satoru Taguchi, Shinya Kaname, Kenichi Yokoyama, Tatsuya Yoshioka, Hiroshi Fukuhara
Publikováno v:
Kidney International Reports, Vol 7, Iss 2, Pp 270-281 (2022)
Introduction: The effects of long-term and uninterrupted tolvaptan treatment on autosomal dominant polycystic kidney disease (ADPKD) are unclear. Therefore, a more than 3-year continuous treatment study was performed. Methods: From the Kyorin Univers
Externí odkaz:
https://doaj.org/article/02a8b3b2c88f4a668c8d9966458138cf
Autor:
Junji Kitamura, Satoru Taguchi, Takatsugu Okegawa, Kazuki Honda, Toshihiko Kii, Yoshihiro Tomida, Ryuki Matsumoto, Naoki Ninomiya, Kazuki Masuda, Yu Nakamura, Tsuyoshi Yamaguchi, Manami Kinjo, Mitsuhiro Tambo, Aya Isomura, Akimasa Hayashi, Hiroshi Kamma, Eiji Higashihara, Junji Shibahara, Hiroshi Fukuhara
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)
Abstract Background Adenosquamous carcinoma of the prostate (ASCP) is an extremely rare and aggressive prostate cancer variant, whose genomic characteristics have not been elucidated. Although liquid biopsy of circulating tumor cells (CTCs) is an eme
Externí odkaz:
https://doaj.org/article/014519cf57c84e1a852be4509d307a77
Autor:
Toshihiko Kii, Satoru Taguchi, Kiyotaka Nagahama, Hiroaki Shimoyamada, Kazuki Honda, Yoshihiro Tomida, Ryuki Matsumoto, Junji Kitamura, Naoki Ninomiya, Kazuki Masuda, Yu Nakamura, Tsuyoshi Yamaguchi, Manami Kinjo, Mitsuhiro Tambo, Takatsugu Okegawa, Eiji Higashihara, Junji Shibahara, Hiroshi Fukuhara
Publikováno v:
IJU Case Reports, Vol 4, Iss 3, Pp 172-175 (2021)
Introduction Median raphe cysts are rare benign lesions of the male genitalia that can develop anywhere along the midline from meatus to anus. They are believed to be caused by a defect in closure of median raphe during embryonic development. These c
Externí odkaz:
https://doaj.org/article/782184108c2b4dc0842432e2060f25f1
Autor:
Eiji Higashihara, Hiroshi Fukuhara, John Ouyang, Jennifer Lee, Kikuo Nutahara, Mistuhiro Tanbo, Tsuyoshi Yamaguchi, Satoru Taguchi, Satoru Muto, Shinya Kaname, Isao Miyazaki, Shigeo Horie
Publikováno v:
Kidney International Reports, Vol 5, Iss 9, Pp 1459-1471 (2020)
Introduction: In the Mayo Imaging Classification (MIC) for autosomal dominant polycystic kidney disease (ADPKD), the height-adjusted total kidney volume (HtTKV) growth rate is estimated for classification. Estimated HtTKV slope, termed as eHTKV-α, i
Externí odkaz:
https://doaj.org/article/9c2964d2e0f24a909a9ee0cfff16b82b
Autor:
Shota Omura, Satoru Taguchi, Shogo Miyagawa, Ryuki Matsumoto, Mio Samejima, Naoki Ninomiya, Kazuki Masuda, Yu Nakamura, Tsuyoshi Yamaguchi, Manami Kinjo, Mitsuhiro Tambo, Takatsugu Okegawa, Eiji Higashihara, Hiroshi Fukuhara
Publikováno v:
BMC Urology, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Although the albumin-to-globulin ratio (AGR) is a promising biomarker for various malignancies, few studies have investigated its prognostic significance for upper tract urothelial carcinoma (UTUC). Methods This retrospective stud
Externí odkaz:
https://doaj.org/article/ef6f32b43ed54f51a8720ba042cbad62
Autor:
Kenji Gonda, Takanori Akama, Takayuki Nakamura, Eiko Hashimoto, Naomi Kyoya, Yuichi Rokkaku, Yuko Maejima, Shoichiro Horita, Kazunoshin Tachibana, Noriko Abe, Tohru Ohtake, Kenju Shimomura, Koji Kono, Shigehira Saji, Seiichi Takenoshita, Eiji Higashihara
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-6 (2019)
Abstract Background Autosomal dominant polycystic kidney disease is defined as an inherited disorder characterized by renal cyst formation due to mutations in the PKD1 or PKD2 gene, whereas tuberous sclerosis complex is an autosomal dominant neurocut
Externí odkaz:
https://doaj.org/article/549c962f85f84f4383118f94fe04f5c2
Autor:
Maria V. Irazabal, Jaime D. Blais, Ronald D. Perrone, Ron T. Gansevoort, Arlene B. Chapman, Olivier Devuyst, Eiji Higashihara, Peter C. Harris, Wen Zhou, John Ouyang, Frank S. Czerwiec, Vicente E. Torres
Publikováno v:
Kidney International Reports, Vol 1, Iss 4, Pp 213-220 (2016)
Patients with slowly progressive autosomal dominant polycystic kidney disease (ADPKD) are unlikely to experience outcomes during randomized controlled trials (RCTs). An image classification of ADPKD into typical (diffuse cyst distribution) class 1A t
Externí odkaz:
https://doaj.org/article/3c5812206ddf438eb09cc9d3003af252
Autor:
Masanori Kugita, Kazuhiro Nishii, Tamio Yamaguchi, Atsushi Suzuki, Yukio Yuzawa, Shigeo Horie, Eiji Higashihara, Shizuko Nagao
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177934 (2017)
Increased intracellular cyclic AMP (cAMP) in renal tubular epithelia accelerates the progression of polycystic kidney disease (PKD). Thus, decreasing cAMP levels by an adenylyl cyclase inhibitory G protein activator is considered to be an effective a
Externí odkaz:
https://doaj.org/article/39875f381abe43868ea0f36b82a656a8
Autor:
Moritoshi Kinoshita, Eiji Higashihara, Haruna Kawano, Ryo Higashiyama, Daisuke Koga, Takafumi Fukui, Nobuhisa Gondo, Takehiko Oka, Kozo Kawahara, Krisztina Rigo, Tim Hague, Kiyonori Katsuragi, Kimiyoshi Sudo, Masahiko Takeshi, Shigeo Horie, Kikuo Nutahara
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0166288 (2016)
Genetic testing of PKD1 and PKD2 is expected to play an increasingly important role in determining allelic influences in autosomal dominant polycystic kidney disease (ADPKD) in the near future. However, to date, genetic testing is not commonly employ
Externí odkaz:
https://doaj.org/article/852e2aefe090466e906eba4ce22fc7eb
Autor:
Eiji Higashihara, Yoshihiro Tomida, Ryuki Matsumoto, Hiroaki Shimoyamada, Mitsuhiro Tambo, Takatsugu Okegawa, Junji Shibahara, Junji Kitamura, Satoru Taguchi, Kiyotaka Nagahama, Kazuki Masuda, Kazuki Honda, Tsuyoshi Yamaguchi, Naoki Ninomiya, Yu Nakamura, Hiroshi Fukuhara, Manami Kinjo, Toshihiko Kii
Publikováno v:
IJU Case Reports, Vol 4, Iss 3, Pp 172-175 (2021)
IJU Case Reports
IJU Case Reports
Introduction Median raphe cysts are rare benign lesions of the male genitalia that can develop anywhere along the midline from meatus to anus. They are believed to be caused by a defect in closure of median raphe during embryonic development. These c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0fbcf8f5143c994bdc19c9a41ef616
https://doi.org/10.1002/iju5.12271
https://doi.org/10.1002/iju5.12271