Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Satoshi Mano"'
Autor:
Hisatsugu Takahara, Satoshi Mano, Daisuke Honda, Yuki Shimizu, Yusuke Suzuki, Hisaki Rinno, Hiroaki Io, Hitoshi Suzuki, Teruo Hidaka, Isao Ohsawa, Masayuki Maiguma, Yasuhiko Tomino
Publikováno v:
Internal Medicine
A 42-year-old Japanese man with hereditary angioedema suffered accidental trauma to his jaw in Shizuoka Prefecture, Japan, which gradually caused facial edema. Since plasma-derived human C1 inhibitor (pdh C1-INH) was unavailable, he had to be transfe
Autor:
Yusuke Suzuki, Yasuhiko Tomino, Yoshikazu Goto, Hiroyuki Inoshita, Tatsuo Shimizu, Isao Ohsawa, Hiromichi Gotoh, Nobuyuki Sato, Yuya Nakamura, Daisuke Honda, Atsuko Hisada, Kisara Onda-Tsueshita, Satoshi Mano
Publikováno v:
Internal Medicine
Objective The present study was designed to identify the clinical characteristics that permit the differential diagnosis of hereditary angioedema (HAE) and mast cell-mediated angioedema (Mast-AE) during the first consultation. Methods The medical his
Autor:
Yasuhiko Tomino, Nobuyuki Sato, Isao Ohsawa, Yusuke Suzuki, Hiroyuki Inoshita, Daisuke Honda, Satoshi Mano
Publikováno v:
Allergology International, Vol 66, Iss 4, Pp 603-609 (2017)
Background Hereditary angioedema (HAE) is an autosomal dominant disease caused by deficiency of C1 esterase inhibitor. Symptoms of HAE include edema, which can potentially cause suffocation. Some patients with HAE exhibit immunological abnormalities,
Autor:
Isao Ohsawa, Yasuhiko Tomino, Atsuko Hisada, Daisuke Honda, Mamiko Shimamoto, Satoshi Mano, Hiroyuki Inoshita, Seiji Nagamachi
Publikováno v:
Allergology International, Vol 63, Iss 4, Pp 595-602 (2014)
Background Hereditary angioedema (HAE) is a rare but life-threatening condition that results from mutations in C1-inhibitor (C1-INH). Since distinguishing HAE from other causes of angioedema (AE) is a critical problem in emergencies, the objective of
Autor:
Hiroyuki Inoshita, Isao Ohsawa, Kisara Onda, Nobuyuki Sato, Gaku Kusaba, Masaya Ishii, Hiroyuki Ohi, Satoshi Mano, Yasuhiko Tomino, Tomohito Gohda, Satoshi Horikoshi
Publikováno v:
Journal of Clinical Laboratory Analysis. 24:113-118
The aim of this study was to explore the association between the serum concentration of complement component 3 (C3) and a variety of metabolic parameters. The study involved 125 patients in our outpatient clinic. Anthropometric and clinical laborator
Autor:
Kiyoshi Matsuoka, Yukihiko Takeda, Miyuki Akiba-Takagi, Isao Ohsawa, Satoshi Horikoshi, Shinya Ogasawara, Masanori Hara, Yasuhiko Tomino, Rin Asao, Yoshiko Nagai-Hosoe, Satoshi Mano, Yoshiaki Hirayama, Takuto Seki, Fumiko Kodama, Sakari Sekine, Katsuhiko Asanuma, Hiroyuki Kurosawa
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN. 7(9)
Podocalyxin (PCX) is present on the apical cell membrane of podocytes and is shed in urine from injured podocytes. Urinary podocalyxin (u-PCX) is associated with severity of active glomerular injury in patients with glomerular diseases. This study ex
Autor:
Teizo Fujita, Isao Ohsawa, Mariko Tamano, Hiroyuki Ohi, Yasuhiko Tomino, Satoshi Horikoshi, Kisara Onda, Akie Toki, Satoshi Mano, Michiro Wakabayashi
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 12, Iss 1, p 64 (2011)
BMC Nephrology, Vol 12, Iss 1, p 64 (2011)
Background Glomerular damage in IgA nephropathy (IgAN) is mediated by complement activation via the alternative and lectin pathways. Therefore, we focused on molecules stabilizing and regulating the alternative pathway C3 convertase in urine which mi