Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE).

Autor: Palao-Ocharan, Paola, Prior, Nieves, Pérez-Fernández, Elia, Caminoa, Magdalena, DV-HAE-QoL Study Group, Aberer, W., Betschel, S., Bygum, A., Campos, R. A., Csuka, D., Farkas, H., Gómez-Traseira, C., Grumach, A. S., Leibovich, I., Malbran, A., Moldovan, D., Mihaly, E., Obtulowicz, K., Porebski, G., Reshef, A.

Publikováno v: Orphanet Journal of Rare Diseases; 3/2/2022, Vol. 17 Issue 1, p1-14, 14p

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency

Autor: Farkas, H, Martinez Saguer, I, Bork, K, Bowen, T, Craig, T, Frank, M, Germenis, Ae, Grumach, As, Luczay, A, Varga, L, Zanichelli, A, Aberer, W, Andrejevic, S, Aygoeren Pürsün, E, Banerji, A, Bara, Na, Bas, M, Bernstein, J, Betschel, S, Björkander, J, Boccon Gibod, I, Bouillet, L, Bova, M, Boysen, Hh, Branco Ferreira, M, Bygum, A, Caballero, T, Cancian, M, Castaldo, A, Christiansen, S, Cicardi, M, Drouet, C, Fabiani, J, Gompels, M, Gonzalez Quevedo MT, Gooi, J, Gower, R, Gökmen, Nm, Grivcheva Panovska, V, Guilarte, M, Gülbahar, O, Hack, E, Hakl, R, Harmat, G, Mjeseňák, M, Jolles, S, Kaplan, A, Katelaris, C, Kosnik, M, Kőhalmi, Kv, Leibovich, I, Levi, M, Li, H, Longhurst, Hj, Lumry, W, Magerl, M, Malbran, A, Martin, L, Maurer, M, Mihály, E, Moldovan, D, Murdjeva, M, Nagy, Ib, Nielsen, Ew, Nieto, S, Nordenfelt, P, Obtulowitzc, K, Pedrosa, M, Porębski, G, Prior, N, Reshef, A, Riedl, Ma, Rosenkranz, B, Schmid Grendelmeier, P, Péter, S, Speletas, M, Staevska, M, Stobiecki, M, Triggiani, Massimo, Veszeli, N, Wuillemin, W, Xiang, Zy, Yamamoto, B, Zuraw, B.

Publikováno v: Allergy
Farkas, H, Martinez-Saguer, I, Bork, K, Bowen, T, Craig, T, Frank, M, Germenis, A E, Grumach, A S, Luczay, A, Varga, L, Zanichelli, A, HAWK & Bygum, A 2017, ' International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency ', Allergy, vol. 72, no. 2, pp. 300–313 . https://doi.org/10.1111/all.13001

BACKGROUND: The consensus documents published to date on hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) have focused on adult patients. Many of the previous recommendations have not been adapted to pediatric patients. We intended to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f408e9ac62b0c266ea781891be1a053c
http://hdl.handle.net/11386/4685338

Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema.

Autor: Jiang, Lingxi^1,2 (AUTHOR), Dai, Chao¹ (AUTHOR), Duan, Suyang¹ (AUTHOR), Wang, Tingting¹ (AUTHOR), Xie, Chunbao¹ (AUTHOR), Zhang, Luhan¹ (AUTHOR), Ye, Zimeng³ (AUTHOR), Ma, Xiumei¹ (AUTHOR) 845102937@qq.com, Shi, Yi^1,2,4,5 (AUTHOR) yshi@uestc.edu.cn

Publikováno v: Orphanet Journal of Rare Diseases. 9/13/2024, Vol. 19 Issue 1, p1-14. 14p.

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Hereditary Angioedema: Novel Molecules for Treatment of Acute Attacks and Long-Term Prophylaxis.

Autor: Covella, Bianca¹ b.covella@miulli.it, Giliberti, Marica² gilibertimarica@gmail.com, Montinaro, Adriano² adrianomontinaro@gmail.com, Rossi, Luigi¹ l.rossi@miulli.it, Montinaro, Vincenzo¹ vincenzo.montinaro1@gmail.com

Publikováno v: Future Pharmacology. Mar2024, Vol. 4 Issue 1, p41-53. 13p.