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Searching for genetic biomarkers for hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE)

511.

Parsopoulou, F., Loules, G., Zamanakou, M., Csuka, D., Szilagyi, A., Kompoti, M., Porebski, G., Psarros, G., Psarros, F., Magerl, M., Valerieva, A., Staevska, M., Obtulowicz, K., Maurer, M., Speletas, M., Farkas, H., and Germenis, A. E.+: Searching for genetic biomarkers for hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE). Front. Allergy 2022: 3; 868185. IF: N/A

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ARIA (Allergic Rhinitis and its Impact on Asthma) – Achievements in 10 years and future needs

71. Bousquet, J., Schünemann, H. J., Samolinski, B., Demoly, P., Baena-Cagnani, C. E., Bachert, C., Bonini, S., Boulet, L.P., Bousquet, P. J., Brozek, J. L., Canonica, G.W., Casale, T. B., Cruz A. A., Fokkens, W. J., Fonseca, J. A., Gerth van Wijk, R., Grouse, L., Haahtela, T., Khaltaev, N., Kuna, P., Lockey, R. F., Lodrup Carlsen, K. C., Mullol, J., Naclerio, R., O’Hehir, R. E., Ohta, K., Palkonen, S., Papadopoulos, N. G., Passalacqua, G., Pawankar, R., Price, D., Ryan, D., Simons, F. E. R., Togias, A., Williams, D., Yorgancioglu, A., Yusuf, O. M., Aberer, W., Adachi, M., Agache, I., Aϊt-Khaled, N., Akdis, C. A., Andrianarisoa, A., Annesi-Maesano, I., Ansotegui, I. J., Baiardini, I., Bateman, E. D., Bedbrook, A., Beghé, B., Beji, M., Bel, E. H., Ben Kheder, A., Bennoor, K. S., Bergmann, K. C., Berrissoul, F., Bieber, T., Bindslev-Jensen, C., Blaiss, M. S., Boner, A. L., Bouchard, J., Braido, F., Brightling, C. E., Bush, A., Caballero, F., Calderon, M. A., Calvo, M. A., Camargos, P. A. M., Caraballo, L. R., Carlsen, K. H., Carr, W., Cepeda, A. M., Cesario, A., Chavannes, N. H., Chen, Y. Z., Chiriac, A. M., Chivato Pérez, T., Chkhartishvili, E., Ciprandi, G., Costa, D. J., Cox, L., Custovic, A., Dahl, R., Darsow, U., De Blay, F., Deleanu, D., Denburg, J. A., Devillier, P., Didi, T., Dokic, D., Dolen, W. K., Douagui, H., Dubakiene, R., Durham, S. R., Dykewicz, M. S., El-Gamal, Y., El-Meziane, A., Emuzyte, R., Fiocchi, A., Fletcher, M., Fukuda, T., Gamkrelidze, A., Gereda, J. E., González Diaz S., Gotua, M., Guzmán, M. A., Hellings, P. W., Hellquist-Dahl, B., Horak, F., Hourihane, J. O’B., Howarth, P., Humbert, M., Ivancevich, J. C., Jackson, C., Just, J., Kalayci, O., Kaliner, M. A., Kalyoncu, A. F., Keil, T., Keith, P. K., Khayat, G., Kim, Y. Y., Koffi N’Goran, B., Koppelman, G. H., Kowalski, M. L., Kull, I., Kvedariene, V., Larenas-Linnemann, D., Le, L. T., Lemière, C., Li, J., Lieberman, P., Lipworth, B., Mahboub, B., Makela, M. J., Martin, F., Marshall, G. D., Martinez, F. D., Masjedi, M. R., Maurer, M., Mavale-Manuel, S., Mazon, A., Melen, E., Melter, E. O., Mendez, N. H., Merk, H., Mihaltan, F., Mohammad, Y., Morais-Almeida, M., Muraro, A., Nafti, S., Namazova-Baranova, L., Nekam, K., Neou, A., Niggemann, B., Nizankowska-Mogilnicka, E., Nyembue, T. D., Okamoto, Y., Okubo, K., Orru, M. P., Ouedraogo, S., Olzdemir, C., Panzner, P., Pali-Schöll, I., Park, S., Pigearias, B., Pohl, W., Popov, T. A., Postma, D. S., Potter, P., Rabe, K. F., Ratomaharo, J., Reitamo, S., Ring, J., Roberts, R., Rogala, B., Romano, A., Roman Rodriguez, M., Rosado-Pinto, J., Rosenwasser, L., Rottem, M., Sánchez-Borges, M., Scadding, G. K., Schmid-Grendelmeier, P., Sheikh, A., Sisul, J. C., Solé, D., Sooronbaev, T., Spicak, V., Spranger, O., Stein, R. T., Stoloff, S. W., Sunyer, J., Szczeklik, A., Todo-Bom, A., Toskala, E., Tremblay, Y., Valena, R., Valero, A. L., Valeyre, D., Valiulis, A., Valovirta, E., Van Cauwenberge, P., Vandenplas, O., van Weel, C. Vichyanond, P., Viegi, G., Wang, D. Y., Wickman, M., Wöhrl, S., Wright, J., Yawn, B. P., Yiallouros, P. K., Zar, H. J., Zernotti, M. E., Zhong, N., Zidarn, M., and Zuberbier, T.: ARIA (Allergic Rhinitis and its Impact on Asthma) – Achievements in 10 years and future needs. J. Allergy Clin. Immunol. 2012: 130; 1049-1062. IF: 12.04
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A mutation in the kringle domain of human factor XII that causes autoinflammation, disturbs zymogen quiescence and accelerates activation

371 Hofman, Z. L. M.*, Clark, C. C.*, Sanrattana, W., Nosairi, A., Parr, N., Zivkovic, M., Krause, K., Mahnke, N. A., Scheffel, J., Hack, C. E., Maurer, M., de Maat, S., and Maas, C.+: A mutation in the kringle domain of human factor XII that causes autoinflammation, disturbs zymogen quiescence and accelerates activation. J. Biol. Chem. 2020: 295; 363-374. IF: 5.16

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Management of chronic spontaneous urticaria: a worldwide perspective

312 Kolkhir, P.+, Pogorelov, D., Darlenski, R., Caminati, M., Tanno, L. K., Le Pham, D., Gonzalez-Estrada, A., Antolin-Amérigo, D., Dimov, V., Weller, K., Sanchez-Borges, M., Ansotegui, I., and Maurer, M.: Management of chronic spontaneous urticaria: a worldwide perspective. World Allergy Organ. J. 2018: 11; 14 eCollection. IF: 3.68

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Hereditäres Angioödem

6. Magerl, M. and Maurer, M.: Hereditäres Angioödem, In: Schöfer, H. and Baur-Beger, S., editors: Derma-Net-Online: Aktuelle Dermatologie für Dermatologen und dermatologisch Interessierte (www.derma-net-online.de), 2007
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