Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Satoshi Mano"'
Publikováno v:
Intractable Rare Dis Res
Hereditary angioedema caused by C1-inhibitor (C1-INH) deficiency (HAE-C1-INH) is a rare autosomal dominant disease. Primary care physicians sometimes face difficulties in diagnosing HAE-C1-INH owing to fluctuations in C1-INH function levels influence
Publikováno v:
Intractable Rare Dis Res
Hereditary angioedema due to C1-inhibitor (C1-INH) deficiency (HAE-C1-INH) induces an acute attack of angioedema. In 2018, icatibant available for self-possession and subcutaneous self-administration was licensed for on-demand treatment in addition t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2e6d7201153647ab45673a8ef35368
https://europepmc.org/articles/PMC8122312/
https://europepmc.org/articles/PMC8122312/
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