Zobrazeno 1 - 10
of 1 669
pro vyhledávání: '"Adatia, A."'
Autor:
Cai, Zhixi, Ghosh, Shreya, Adatia, Aman Pankaj, Hayat, Munawar, Dhall, Abhinav, Gedeon, Tom, Stefanov, Kalin
The detection and localization of highly realistic deepfake audio-visual content are challenging even for the most advanced state-of-the-art methods. While most of the research efforts in this domain are focused on detecting high-quality deepfake ima
Externí odkaz:
http://arxiv.org/abs/2311.15308
Autor:
Adil Adatia, Jean-Nicolas Boursiquot, Dawn Goodyear, Chrystyna Kalicinsky, Amin Kanani, Susan Waserman, Michelle M. L. Nguyen, Abhinav Wadhwa, Jessica Weiss, Ahmed El-Zoeiby, Stephen Betschel
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-10 (2024)
Abstract Background Hereditary angioedema with normal C1-inhibitor function (HAE nC1-INH) and idiopathic angioedema of unknown etiology (AE-UNK) are rare conditions that cause recurrent subcutaneous and submucosal swelling. The characteristics and cl
Externí odkaz:
https://doaj.org/article/2fb08afda580450ba465e4bced14692b
Autor:
Adil Adatia, Markus Magerl
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/645d1eea643b4b56a58da55c760f7639
Autor:
Justin J. Y. Kim, Liz Dennett, Maria B. Ospina, Anne Hicks, Harissios Vliagoftis, Adil Adatia
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-13 (2024)
Abstract Purpose Immunoglobulin replacement therapy is a standard treatment for patients with antibody production deficiencies, which is of interest in patients with chronic obstructive pulmonary disease (COPD). This systematic review, registered wit
Externí odkaz:
https://doaj.org/article/d48a511902d14e708356cfe46282e5c2
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Hereditary angioedema due to C1 inhibitor deficiency (HAE) is a rare inborn error of immunity that presents with episodic swelling. Management is multifaceted and includes on-demand treatment of swelling episodes, short-term prophylaxis to prevent sw
Externí odkaz:
https://doaj.org/article/ade8c777fb7142388d3b25abc77f0a9b
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-5 (2024)
Abstract Background Asthma is a common respiratory illness affecting 2.8 million Canadians, including 9.7% of Albertans. Prior studies showed a substantial decrease in ED visits for asthma in the decade preceding 2010, followed by a stabilization. Th
Externí odkaz:
https://doaj.org/article/bc607a7e596949c18b70bf2010e7a768
Autor:
Adatia, Adil1 (AUTHOR), Boursiquot, Jean-Nicolas2 (AUTHOR), Goodyear, Dawn3 (AUTHOR), Kalicinsky, Chrystyna4 (AUTHOR), Kanani, Amin5 (AUTHOR), Waserman, Susan6 (AUTHOR), Nguyen, Michelle M. L.7 (AUTHOR), Wadhwa, Abhinav8 (AUTHOR), Weiss, Jessica7 (AUTHOR), El-Zoeiby, Ahmed8 (AUTHOR), Betschel, Stephen9 (AUTHOR) stephen.betschel@unityhealth.to
Publikováno v:
Allergy, Asthma & Clinical Immunology. 9/27/2024, Vol. 20 Issue 1, p1-10. 10p.
Autor:
Buchholz, Connor, Bell, Lauren A., Adatia, Safina, Bagley, Sarah M., Wilens, Timothy E., Nurani, Alykhan, Hadland, Scott E.
Publikováno v:
In Journal of Adolescent Health February 2024 74(2):320-326
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundHereditary angioedema due to C1 inhibitor deficiency is a rare genetic condition that causes recurrent swelling with consequent functional impairment and decreased quality of life. Long-term prophylaxis (LTP) to prevent angioedema episodes
Externí odkaz:
https://doaj.org/article/6d5a4bb773cf4f118353ff6557552778
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