Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Daisuke Honda"'
Autor:
Daisuke Honda, MD, PhD, Michihiro Hide, MD, PhD, Tomoo Fukuda, MD, PhD, Keisuke Koga, MD, PhD, Eishin Morita, MD, PhD, Shinichi Moriwaki, MD, Yoshihiro Sasaki, MD, PhD, Yusuke Suzuki, MD, PhD, Phil Collis, PhD, Douglas T. Johnston, DO, Dianne Tomita, MPH, Bhavisha Desai, PharmD, Isao Ohsawa, MD, PhD
Publikováno v:
World Allergy Organization Journal, Vol 17, Iss 3, Pp 100882- (2024)
Background: Berotralstat is a once-daily oral inhibitor of plasma kallikrein for the prophylaxis of hereditary angioedema (HAE) in patients ≥12 years. APeX-J aimed to evaluate the efficacy and safety of berotralstat in Japan. Methods: APeX-J was a
Externí odkaz:
https://doaj.org/article/3b4e2445fcc64daeb7ca4e24132a6cc4
Autor:
Daisuke Honda, Isao Ohsawa, Toshiyuki Miyata, Masayuki Ozaki, Masashi Aizawa, Yasuhiko Tomino, Katsuhiko Asanuma
Publikováno v:
Allergology International, Vol 73, Iss 1, Pp 174-176 (2024)
Externí odkaz:
https://doaj.org/article/0a1a8dc9764b416ea801e13a1b9e4abe
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-4 (2023)
Abstract Background Hereditary angioedema (HAE), which is caused by C1-inhibitor (C1-INH) deficiency or dysfunction, is a rare and potentially life-threatening disease. In patients with HAE, excess production of bradykinin causes acute unpredictable
Externí odkaz:
https://doaj.org/article/70302f21a9c2481d9e5567022db29adf
Autor:
Maiko Akira, Hitoshi Suzuki, Arisa Ikeda, Masako Iwasaki, Daisuke Honda, Hisatsugu Takahara, Hisaki Rinno, Shigeki Tomita, Yusuke Suzuki
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/d62d19e22760475bb4555ceae0c7b418
Autor:
Maiko Akira, Hitoshi Suzuki, Arisa Ikeda, Masako Iwasaki, Daisuke Honda, Hisatsugu Takahara, Hisaki Rinno, Shigeki Tomita, Yusuke Suzuki
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-5 (2021)
Abstract Background Nephronophthisis (NPHP) is a chronic tubular interstitial disorder that exhibits an autosomal recessive genetic form and causes progressive renal failure in children. Patients with NPHP rarely show urinary abnormalities, edema, or
Externí odkaz:
https://doaj.org/article/36b93002ee064a9faf676b1bbd95adb4
Autor:
Kazumasa Iwamoto, Beverley Yamamoto, Isao Ohsawa, Daisuke Honda, Takahiko Horiuchi, Akira Tanaka, Atsushi Fukunaga, Junichi Maehara, Kouhei Yamashita, Tomoyuki Akita, Michihiro Hide
Publikováno v:
Allergology International, Vol 70, Iss 2, Pp 235-243 (2021)
Background: The rate at which patients are accurately diagnosed with hereditary angioedema (HAE), as well as diagnosed patients access to modern treatments differs greatly among countries. Moreover, the severity and burden of HAE on patients have bee
Externí odkaz:
https://doaj.org/article/e313e5de8b5848dd9fd3e3b88d292e59
Autor:
Isao Ohsawa, Atsushi Fukunaga, Shinya Imamura, Kazumasa Iwamoto, Akio Tanaka, Michihiro Hide, Daisuke Honda, Kouhei Yamashita, Chisako Fujiwara, Osamu Ishikawa, Takeo Yamaguchi, Junichi Maehara, Tomoya Hirose, Masahiro Ieko, Kunihiko Umekita, Yuya Nakamura, Hiromichi Gotoh
Publikováno v:
World Allergy Organization Journal, Vol 14, Iss 2, Pp 100511- (2021)
Background: Hereditary angioedema (HAE) is a rare but life-threatening condition. HAE types I and II (HAE-1/2) result from C1-inhibitor (C1–INH) deficiency. However, recent genetic analysis has established a new type of HAE with normal C1–INH (HA
Externí odkaz:
https://doaj.org/article/ee7b812df59041f487c84ec1e836eea0
Autor:
Daisuke Honda, Isao Ohsawa, Nobuyuki Sato, Hiroyuki Inoshita, Satoshi Mano, Yasuhiko Tomino, Yusuke Suzuki
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
Externí odkaz:
https://doaj.org/article/619aa16a139646c98046f7bf9196171f
Autor:
Isao Ohsawa, Daisuke Honda, Seiji Nagamachi, Atsuko Hisada, Mamiko Shimamoto, Hiroyuki Inoshita, Satoshi Mano, Yasuhiko Tomino
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 o
Externí odkaz:
https://doaj.org/article/51f33d6e8c084f79a9c47d34c69eab51
Autor:
Junichiro James Kazama, Fumihiko Koiwa, Keitaro Yokoyama, Masafumi Fukagawa, Kenji Asano, Daisuke Honda, Tadao Akizawa
Publikováno v:
Clinical Pharmacokinetics. 61:1271-1284
Upacicalcet is a new renally excreted and injectable calcimimetic agent. We evaluated the pharmacokinetics, pharmacodynamics, safety, and tolerability of single and multiple intravenous administration of upacicalcet in patients with secondary hyperpa