Zobrazeno 1 - 10
of 20
pro vyhledávání: '"George, Harmat"'
Autor:
Ibolya Czaller, Henriette Farkas, Szilvia Valentin, George Füst, Beáta Visy, Dorottya Csuka, László Jakab, Gábor Széplaki, Lilian Varga, George Harmat, István Karádi, Anikó Vas, Zoltán Prohászka
Publikováno v:
European Journal of Clinical Pharmacology
European Journal of Clinical Pharmacology, Springer Verlag, 2009, 66 (4), pp.419-426. ⟨10.1007/s00228-009-0771-z⟩
European Journal of Clinical Pharmacology, Springer Verlag, 2009, 66 (4), pp.419-426. ⟨10.1007/s00228-009-0771-z⟩
Danazol is a drug most widely used for the prophylaxis of hereditary angioedema resulting from the deficiency of the C1-inhibitor. Potential hepatotoxic or liver tumor-inducing side effects of long-term danazol prophylaxis have been investigated duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0747f1c753dfcbcc49f69c092972cad9
https://doi.org/10.1007/s00228-009-0771-z
https://doi.org/10.1007/s00228-009-0771-z
Publikováno v:
Pediatrics. 120:e713-e722
Hereditary angioneurotic edema is a rare disorder caused by the congenital deficiency of C1 inhibitor. Recurring angioedematous paroxysms that most commonly involve the subcutis (eg, extremities, face, trunk, and genitals) or the submucosa (eg, intes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::446e4b3f97756e503dd529bcf4522536
https://doi.org/10.1542/peds.2006-3303
https://doi.org/10.1542/peds.2006-3303
Autor:
Gábor Széplaki, László Cervenak, Julianna Németh, George Harmat, István Karádi, Lilian Varga, Katalin Miklós, Henriette Farkas, George Füst, Beáta Visy
Publikováno v:
Molecular Immunology. 44:1454-1460
The presence of autoantibodies to C1-inhibitor (C1-INH-Abs) is a hallmark of acquired C1-inhibitor deficiency. However, only scarce data are available on their prevalence in hereditary angioedema (HAE). In a prospective study performed between 2001 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beb536f7ea9ddaa9651b530e951aa870
https://doi.org/10.1016/j.molimm.2006.04.020
https://doi.org/10.1016/j.molimm.2006.04.020
Autor:
Peter J. Späth, E. Rusicke, Christoph Bucher, Alvaro Blanch, Olga Roche, Emanuela Pappalardo, István Karádi, Marco Cicardi, Mathias Juers, Inmaculada Martinez-Saguer, Roberto Giacomelli, Pál Novák Kaposi, Anthony J. Castaldo, Erik Waage Nielsen, Roberto Perricone, Arianna Kitzinger, Kalman Fay, Emel Aygören-Pürsün, Carlo Perricone, Christian Drouet, George Füst, Beáta Visy, C. Erik Hack, Vincenzo Penna, Hilary Longhurst, Tímea Kollár, George Harmat, István Nagy, Nicole Monnier, Éva Németh, Jan H. Nuijens, Bettina Fischer, Ursula Rauch, Peter L. Lakatos, Caterina De Carolis, Caroline O'Grady, Edit Takács, Margarita López-Trascasa, Henriette Farkas, Albrecht Gröner, George Szendei, Lilian Varga, Alvin E. Davis, Lennart Truedsson, Béla Fekete, John Jakenfelds, Andrea Zanichelli, Wolfhart Kreuz, Kayla Williams, Lajos Kalmar, Lorenza C. Zingale, Karen Binkley, Christiane Duponchel, Laurence Bouillet, Attila Tordai, Luigi Fontana, Angelo Agostoni, Konrad Bork
Publikováno v:
The Journal of Allergy and Clinical Immunology
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of facial, laryngeal, genital, or peripheral swelling or abdominal pain secondary to intra-abdominal edema. Resulting from mutations affecting C1 esterase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::683368948c5151ac254b136230a7bd26
https://doi.org/10.1016/j.jaci.2004.06.047
https://doi.org/10.1016/j.jaci.2004.06.047
Publikováno v:
Pediatric Allergy and Immunology. 13:153-161
Hereditary angio-oedema (HAE) results from the deficiency of C1-esterase inhibitor (C1-INH). The clinical picture of this autosomal dominant disorder is characterized by recurrent attacks of subcutaneous oedema and/or potentially life-threatening swe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6460e2fcdb524a527ebeaeff57499c
https://doi.org/10.1034/j.1399-3038.2002.01014.x
https://doi.org/10.1034/j.1399-3038.2002.01014.x
Autor:
Lajos Jakab, George Harmat, Erika Szabó, György Temesszentandrási, Henriette Farkas, Dorottya Csuka, Lilian Varga, István Karádi, Z. Nébenfűhrer, Zsuzsanna Zotter
Publikováno v:
Allergy.
Background Hereditary angioedema is a potentially life-threatening disorder, because edema occurring in the mucosa of the upper airways can lead to suffocation. The management of HAE consists of avoiding the triggering factors, prophylaxis, and the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ba86372316c3833cd346374b92c0d9
https://doi.org/10.1111/all.12032
https://doi.org/10.1111/all.12032
Autor:
Henriette Farkas, Ibolya Czaller, George Harmat, Erika Szabó, Dorottya Csuka, Lilian Varga, George Füst, János Fejes, Zsuzsanna Zotter
Publikováno v:
The Journal of allergy and clinical immunology. 131(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6f1d1d39e3c8527997d45a1118d57e4
https://pubmed.ncbi.nlm.nih.gov/23063583
https://pubmed.ncbi.nlm.nih.gov/23063583
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:
Lilian, Varga, Gábor, Széplaki, Beáta, Visy, George, Füst, George, Harmat, Katalin, Miklós, Julianna, Németh, László, Cervenak, István, Karádi, Henriette, Farkas
Publikováno v:
Molecular immunology. 44(6)
The presence of autoantibodies to C1-inhibitor (C1-INH-Abs) is a hallmark of acquired C1-inhibitor deficiency. However, only scarce data are available on their prevalence in hereditary angioedema (HAE). In a prospective study performed between 2001 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bcfcfef34b7d01c0f30a281ca332920
https://pubmed.ncbi.nlm.nih.gov/16750855
https://pubmed.ncbi.nlm.nih.gov/16750855
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eec911d1cae8a42535d99387a117b91f
https://doi.org/10.1055/s-2005-917428
https://doi.org/10.1055/s-2005-917428