Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiencyFarkas, H. ; Martinez‐Saguer, I. ; Bork, K. ; Bowen, T. ; Craig, T. ; Frank, M. ; Germenis, A. E. ; Grumach, A. S. ; Luczay, A. ; Varga, L. ; Zanichelli, A. ; Aberer, Werner ; Andrejevic, Sladjana ; Aygoeren‐Pürsün, Emel ; Banerji, Alena ; Bara, Noemi‐Anna ; Bas, Murat ; Bernstein, Jonathan ; Betschel, Stephen ; Björkander, Janne ; Boccon‐Gibod, Isabelle ; Bouillet, Laurence ; Bova, Maria ; Boysen, Henrik Halle ; Branco‐Ferreira, Manuel ; Bygum, Anette ; Caballero, Teresa ; Cancian, Mauro ; Castaldo, Anthony ; Christiansen, Sandra ; Cicardi, Marco ; Drouet, Christian ; Fabiani, Jose ; Gompels, Mark ; Gonzalez‐Quevedo, Maria Teresa ; Gooi, Jimmy ; Gower, Richard ; Gökmen, Nihal Mete ; Grivcheva‐Panovska, Vesna ; Guilarte, Mar ; Gülbahar, Okan ; Hack, Erik ; Hakl, Roman ; Harmat, György ; Jeseňák, Miloš ; Jolles, Stephen ; Kaplan, Allen ; Katelaris, Connie ; Kosnik, Mitja ; Kőhalmi, Kinga Viktória ; Leibovich, Iris ; Levi, Marcel ; Li, Henry ; Longhurst, Hilary J. ; Lumry, William ; Magerl, Markus ; Malbran, Alejandro ; Martin, Ludovic ; Maurer, Marcus ; Mihály, Enikő ; Moldovan, Dumitru ; Murdjeva, Mariana ; Nagy, Imola Beatrix ; Nielsen, Erik W. ; Nieto, Sandra ; Nordenfelt, Patrik ; Obtulowitzc, Kristine ; Pedrosa, Maria ; Porębski, Grzegorz ; Prior, Nieves ; Reshef, Avner ; Riedl, Marc A. ; Rosenkranz, Bernd ; Schmid‐Grendelmeier, Peter ; Péter, Spath ; Speletas, Matthaios ; Staevska, Maria ; Stobiecki, Marcin ; Triggiani, Massimo ; Veszeli, Nóra ; Wuillemin, Walter ; Xiang, Zhi Yu ; Yamamoto, Beverley ; Zuraw, BruceAllergy, 2017-02, Vol.72 (2), p.300-313 [Peer Reviewed Journal]Denmark: Blackwell Publishing LtdFull text available |
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2 |
Material Type: Article
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Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiencyBork, Konrad, MD ; Hardt, Jochen, PhD ; Witzke, Günther, PhDJournal of allergy and clinical immunology, 2012-09, Vol.130 (3), p.692-697 [Peer Reviewed Journal]New York, NY: Mosby, IncFull text available |
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3 |
Material Type: Article
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The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiencyRupar, Nina ; Šelb, Julij ; Košnik, Mitja ; Zidarn, Mihaela ; Andrejević, Slađana ; Čulav, Ljerka ; Grivčeva‐Panovska, Vesna ; Korošec, Peter ; Rijavec, MatijaGene, 2024-08, Vol.919, p.148496-148496, Article 148496 [Peer Reviewed Journal]Netherlands: Elsevier B.VFull text available |
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4 |
Material Type: Article
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Hereditary angio-oedema in Denmark: a nationwide surveyBygum, A.British journal of dermatology (1951), 2009-11, Vol.161 (5), p.1153-1158 [Peer Reviewed Journal]Oxford, UK: Blackwell Publishing LtdFull text available |
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5 |
Material Type: Article
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Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacksCraig, Timothy J., MD ; Levy, Robyn J., MD ; Wasserman, Richard L., PhD, MD ; Bewtra, Againdra K., MD ; Hurewitz, David, MD ; Obtułowicz, Krystyna, MD ; Reshef, Avner, MD ; Ritchie, Bruce, MD ; Moldovan, Dumitru, MD ; Shirov, Todor, MD ; Grivcheva-Panovska, Vesna, MD ; Kiessling, Peter C., PhD ; Keinecke, Heinz-Otto, MS ; Bernstein, Jonathan A., MDJournal of allergy and clinical immunology, 2009-10, Vol.124 (4), p.801-808 [Peer Reviewed Journal]New York, NY: Mosby, IncFull text available |
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6 |
Material Type: Article
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High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiencySuffritti, C. ; Zanichelli, A. ; Maggioni, L. ; Bonanni, E. ; Cugno, M. ; Cicardi, M.Clinical and experimental allergy, 2014-12, Vol.44 (12), p.1503-1514 [Peer Reviewed Journal]England: Blackwell Publishing LtdFull text available |
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7 |
Material Type: Article
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Elevated plasma levels of vascular permeability factors in C1 inhibitor‐deficient hereditary angioedemaLoffredo, S. ; Bova, M. ; Suffritti, C. ; Borriello, F. ; Zanichelli, A. ; Petraroli, A. ; Varricchi, G. ; Triggiani, M. ; Cicardi, M. ; Marone, G.Allergy (Copenhagen), 2016-07, Vol.71 (7), p.989-996 [Peer Reviewed Journal]Denmark: Blackwell Publishing LtdFull text available |
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8 |
Material Type: Article
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Clinical features of hereditary angioedema and warning signs (H4AE) for its identificationGiavina-Bianchi, Pedro ; Aun, Marcelo Vivolo ; Garcia, Juliana Fóes Bianchini ; Gomes, Laís Souza ; Ribeiro, Ana Júlia ; Takejima, Priscila ; Agondi, Rosana Câmara ; Kalil, Jorge ; Motta, Antonio AbilioClinics (São Paulo, Brazil), 2022-01, Vol.77, p.100023-100023, Article 100023 [Peer Reviewed Journal]United States: Elsevier España, S.L.UFull text available |
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9 |
Material Type: Article
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F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedemaSpeletas, M. ; Szilágyi, Á. ; Csuka, D. ; Koutsostathis, N. ; Psarros, F. ; Moldovan, D. ; Magerl, M. ; Kompoti, M. ; Varga, L. ; Maurer, M. ; Farkas, H. ; Germenis, A. E.Allergy (Copenhagen), 2015-12, Vol.70 (12), p.1661-1664 [Peer Reviewed Journal]Denmark: Blackwell Publishing LtdFull text available |
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10 |
Material Type: Article
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The relationship between anxiety and quality of life in children with hereditary angioedemaKessel, Aharon ; Farkas, Henriette ; Kivity, Shmuel ; Veszeli, Nóra ; Kőhalmi, Kinga V. ; Engel‐Yeger, BatyaPediatric allergy and immunology, 2017-11, Vol.28 (7), p.692-698 [Peer Reviewed Journal]England: Wiley Subscription Services, IncFull text available |