Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Michael E. Manning"'
Autor:
Jonathan A. Bernstein, Huamin Henry Li, Timothy J. Craig, Michael E. Manning, John-Philip Lawo, Thomas Machnig, Girishanthy Krishnarajah, Moshe Fridman
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 15, Iss 1, Pp 1-9 (2019)
Abstract Introduction For prophylaxis of hereditary angioedema (HAE) attacks, replacement therapy with human C1-inhibitor (C1-INH) treatment is approved and available as intravenous [C1-INH(IV)] (Cinryze®) and subcutaneous [C1-INH(SC)] HAEGARDA® pr
Externí odkaz:
https://doaj.org/article/873c84b960bf4a1383c8018a2ffd5217
Autor:
Timothy J Craig, Avner Reshef, H Henry Li, Joshua S Jacobs, Jonathan A Bernstein, Henriette Farkas, William H Yang, Erik S G Stroes, Isao Ohsawa, Raffi Tachdjian, Michael E Manning, William R Lumry, Inmaculada Martinez Saguer, Emel Aygören-Pürsün, Bruce Ritchie, Gordon L Sussman, John Anderson, Kimito Kawahata, Yusuke Suzuki, Petra Staubach, Regina Treudler, Henrike Feuersenger, Fiona Glassman, Iris Jacobs, Markus Magerl
Publikováno v:
The Lancet. 401:1079-1090
Autor:
Timothy Craig, Avner Reshef, Huamin Henry Li, Joshua S. Jacobs, Jonathan A. Bernstein, Henriette Farkas, William H. Yang, Erik Stroes, Isao Ohsawa, Raffi Tachdjian, Michael E. Manning, William R. Lumry, Inmaculada Martinez Saguer, Emel Aygören-Pürsün, Bruce Ritchie, Gordon L. Sussman, John Anderson, Kimito Kawahata, Yusuke Suzuki, Petra Staubach, Regina Treudler, Henrike Feuersenger, Fiona Glassman, Iris Jacobs, Markus Magerl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08ef1a615b3d0e2b213435ca175bf48e
https://doi.org/10.2139/ssrn.4336148
https://doi.org/10.2139/ssrn.4336148
Autor:
Michael E. Manning
Publikováno v:
Dermatology and Therapy
Objective The goal of this article is to discuss the importance of differentiating hereditary angioedema (HAE) from other types of angioedema, describe advances in HAE management, especially long-term prophylaxis (LTP), and offer practical recommenda
Autor:
Lauré M. Fijen, Marc A. Riedl, Laura Bordone, Jonathan A. Bernstein, Jason Raasch, Raffi Tachdjian, Timothy Craig, William R. Lumry, Michael E. Manning, Veronica J. Alexander, Kenneth B. Newman, Alexey Revenko, Brenda F. Baker, Charvi Nanavati, A. Robert MacLeod, Eugene Schneider, Danny M. Cohn
Publikováno v:
The New England journal of medicine, 386(11), 1026-1033. Massachussetts Medical Society
BACKGROUND: Hereditary angioedema is characterized by recurrent and unpredictable swellings that are disabling and potentially fatal. Selective inhibition of plasma prekallikrein production by antisense oligonucleotide treatment (donidalorsen) may re
Autor:
Laurie Lee, Michael E. Manning, Neal Sule, Maggie Tabberer, Ian D. Pavord, David M. Mannino, Andrew Fowler, John Oppenheimer, Nicola A. Hanania, Mark Millard, Robert A. Nathan, Guy Peachey, Edward Kerwin, Huib A. M. Kerstjens, Agne Zarankaite
Publikováno v:
Chest. 158:A35-A38
Autor:
Avner Reshef, Teresa Caballero, John Anderson, Ingo Pragst, Subhransu Prusty, Lawrence B. Schwartz, Henrike Feuersenger, Marco Cicardi, James R. Baker, Michael E. Manning, Donald Levy, I. Hussain
Publikováno v:
Pediatric Allergy, Immunology, and Pulmonology
Background: Hereditary angioedema (HAE) due to C1 inhibitor (C1INH) deficiency is characterized by recurrent attacks of edema of the skin and mucosal tissues. Symptoms usually present during childhood (mean age at first attack, 10 years). Earlier sym
Autor:
Christina Ciaccio, Alan B. Goldsobel, Aikaterini Anagnostou, Kirsten Beyer, Thomas B. Casale, Antoine Deschildre, Montserrat Fernández-Rivas, Jonathan O'B. Hourihane, Marta Krawiec, Jay Lieberman, Amy M. Scurlock, Brian P. Vickery, Alex Smith, Stephen A. Tilles, Daniel C. Adelman, Kari R. Brown, Amal H. Assa'ad, David I. Bernstein, J. Andrew Bird, Tara F. Carr, Warner W. Carr, Amarjit S. Cheema, Jonathan Corren, Amy Liebl Darter, Morna J. Dorsey, Stanley M. Fineman, David M. Fleischer, Stephen B. Fritz, Shaila U. Gogate, Alexander N. Greiner, Frank C. Hampel, Joshua S. Jacobs, Sanjeev Jain, Kirsi Jarvinen-Seppo, David K. Jeong, Douglas T. Johnston, Rita Kachru, Edwin H. Kim, Majed Koleilat, Bruce J. Lanser, Stephanie A. Leonard, Mary C. Maier, Michael E. Manning, Lyndon E. Mansfield, Jonathan Matz, Kari Nadeau, Jason A. Ohayon, Elena Perez, Daniel H. Petroni, Stephen J. Pollard, Punita Ponda, Jay M. Portnoy, Rima Rachid, Paul H. Ratner, Rachel Robison, Ned T. Rupp, Georgiana M. Sanders, Hemant P. Sharma, Ellen R. Sher, Lawrence D. Sher, Mandel Sher, Wayne G. Shreffler, Dareen D. Siri, Helen S. Skolnick, Weily Soong, Daniel F. Soteres, Jonathan M. Spergel, Allan Stillerman, Gordon L. Sussman, Jonathan Tam, Pooja Varshney, Susan Waserman, Hugh H. Windom, Robert Wood, William H. Yang
Publikováno v:
Annals of Allergy, Asthma & Immunology. 129:758-768.e4
Autor:
Michael E Manning, Jay M Kashkin
Publikováno v:
Allergy and asthma proceedings. 42(4)
Background: Hereditary angioedema (HAE) is a rare genetic disorder characterized by unpredictable and potentially life-threatening episodes of swelling in various parts of the body. These attacks can be painful and debilitating, and affect a patient'
Autor:
Michael E Manning
Publikováno v:
Allergy and asthma proceedings. 41(Suppl 1)
Hereditary angioedema is a rare, autosomal dominant genetic disorder that leads to sporadic episodes of swelling, which can affect any part of the body. With a prevalence of 1 in 10,000 to 1 in 50,000, there are other, more common causes of angioedem