Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jeanne Burnham"'
Autor:
William H. Yang, Andrew C. Issekutz, Mike MacSween, Tony Giulivi, Nancy McCombie, Nick Karitsiotis, Richard Warrington, Tom Bowen, Jacques Hébert, Bruce Ritchie, Jeanne Burnham
Publikováno v:
Transfusion and Apheresis Science. 29:205-214
C1 esterase inhibitor (C1-INH) deficiency is a rare disorder that lacks consensus for diagnosis therapy and management. Recognizing that Canada is behind the European approach to this disorder, we have formed the Canadian Hereditary Angioedema Societ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4e4dd8a463a511e78f4b321fdfc9f0c
https://doi.org/10.1016/j.transci.2003.08.009
https://doi.org/10.1016/j.transci.2003.08.009
Autor:
Amin Kanani, Georges-Etienne Rivard, Palinder Kamra, Zhi Yu Xiang, Paul K. Keith, Karen A. Valentine, Sean R. Mace, Dumitru Moldovan, Kristylea Brosz, Richard Warrington, Azza Hamed, Inmaculada Martinez-Saguer, Andrew C. Issekutz, Lucia Celeste, Christine McCusker, Ellie Tsai, Man-Chiu Poon, Bazir Serushago, Laurence Bouillet, Erik Waage Nielsen, Bruce L. Zuraw, Teresa Caballero, Gina Lacuesta, Eric Wagner, Jeanne Burnham, István Nagy, Susan Waserman, Wolfhart Kreuz, E. Rusicke, Bruce Ritchie, Peter J. Späth, Lilian Varga, Eric Leith, Christoph Bucher, Chrystyna Kalicinsky, Michael M. Frank, Donald Stark, Doris Neurath, Emel Aygören-Pürsün, David Page, John M. Dean, Marco Cicardi, Lorenza C. Zingale, George Füst, Karen Binkley, Henry Li, Patrik Nordenfelt, Konrad Bork, R. Robert Schellenberg, Tom Bowen, Henriette Farkas, Silvia Marchesin, Jacques Hébert, Hilary Longhurst, George Harmat, Peggy Adomaitis, Sara Smith-Foltz, William H. Yang
Publikováno v:
Scopus-Elsevier
Background We published the Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor [C1-INH] deficiency) in 2004. Objective To ensure that this consensus remains current.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7bd172f6ecc50275a7819af21b7948
https://pubmed.ncbi.nlm.nih.gov/18220150
https://pubmed.ncbi.nlm.nih.gov/18220150
Autor:
Tom, Bowen, Marco, Cicardi, Henriette, Farkas, Konrad, Bork, Wolfhart, Kreuz, Lorenza, Zingale, Lilian, Varga, Inmaculada, Martinez-Saguer, Emel, Aygören-Pürsün, Karen, Binkley, Bruce, Zuraw, Alvin, Davis, Jacques, Hebert, Bruce, Ritchie, Jeanne, Burnham, Anthony, Castaldo, Alejandra, Menendez, Istvan, Nagy, George, Harmat, Christoph, Bucher, Gina, Lacuesta, Andrew, Issekutz, Richard, Warrington, William, Yang, John, Dean, Amin, Kanani, Donald, Stark, Christine, McCusker, Eric, Wagner, Georges-Etienne, Rivard, Eric, Leith, Ellie, Tsai, Michael, MacSween, John, Lyanga, Bazir, Serushago, Art, Leznoff, Susan, Waserman, Jean, de Serres
Publikováno v:
The Journal of allergy and clinical immunology. 114(3)
C1 inhibitor deficiency (hereditary angioedema [HAE]) is a rare disorder for which there is a lack of consensus concerning diagnosis, therapy, and management, particularly in Canada. European initiatives have driven the approach to managing HAE with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d07c9f3f7d1f833e5d7af717978c4de2
https://pubmed.ncbi.nlm.nih.gov/15806017
https://pubmed.ncbi.nlm.nih.gov/15806017