1. A new, quantitative ELISA method for studying the function of the human C1-inhibitor. (October 2018) Authors: Gulyás, Dominik; Veszeli, Nora; Kajdácsi, Erika; Koncz, Anna; Cervenak, László; Gál, Péter; Dobó, József; Farkas, Henriette; Varga, Lilian Journal: Molecular immunology Issue: Volume 102(2018:Oct.) Page Start: 225 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A review of berotralstat for the treatment of hereditary angioedema. (1st February 2023) Authors: Farkas, Henriette; Balla, Zsuzsanna Journal: Expert review of clinical immunology Issue: Volume 19:Number 2(2023) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An investigational oral plasma kallikrein inhibitor for on-demand treatment of hereditary angioedema: a two-part, randomised, double-blind, placebo-controlled, crossover phase 2 trial. Issue 10375 (11th February 2023) Authors: Aygören-Pürsün, Emel; Zanichelli, Andrea; Cohn, Danny M; Cancian, Mauro; Hakl, Roman; Kinaciyan, Tamar; Magerl, Markus; Martinez-Saguer, Inmaculada; Stobiecki, Marcin; Farkas, Henriette; Kiani-Alikhan, Sorena; Grivcheva-Panovska, Vesna; Bernstein, Jonathan A; Li, H Henry; Longhurst, Hilary J; Aud... Journal: Lancet Issue: Volume 401:Issue 10375(2023) Page Start: 458 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biological therapy in hereditary angioedema: transformation of a rare disease. (3rd May 2020) Authors: Longhurst, Hilary; Farkas, Henriette Journal: Expert opinion on biological therapy Issue: Volume 20:Number 5(2020) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency. Issue 1 (December 2015) Authors: Csuka, Dorottya; Veszeli, Nóra; Imreh, Éva; Zotter, Zsuzsanna; Skopál, Judit; Prohászka, Zoltán; Varga, Lilian; Farkas, Henriette Journal: Orphanet journal of rare diseases Issue: Volume 9:Issue 1(2014) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Conestat alfa: an orphan drug for the treatment of hereditary angioedema. (2nd April 2016) Authors: Farkas, Henriette Journal: Expert opinion on orphan drugs Issue: Volume 4:Number 4(2016:Apr.) Page Start: 443 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Continued icatibant use across recurrent attacks in adolescents with hereditary angioedema. Issue 6 (11th May 2021) Authors: Farkas, Henriette; Reshef, Avner; Caballero, Teresa; Ortega López, María C.; Kessel, Aharon; Vardi, Moshe; Hao, James; Aberer, Werner Editors: Atanaskovic‐Markovic, Marina Journal: Pediatric allergy and immunology Issue: Volume 32:Issue 6(2021) Page Start: 1392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Current pharmacotherapy of bradykinin-mediated angioedema. (April 2013) Authors: Farkas, Henriette Journal: Expert opinion on pharmacotherapy Issue: Volume 14:Number 5(2013) Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence. Issue 8 (27th April 2020) Authors: Maurer, Marcus; Aberer, Werner; Agondi, Rosana; Al‐Ahmad, Mona; Al‐Nesf, Maryam Ali; Ansotegui, Ignacio; Arnaout, Rand; Arruda, Luisa Karla; Asero, Riccardo; Aygören‐Pürsün, Emel; Banerji, Aleena; Bauer, Andrea; Ben‐Shoshan, Moshe; Berardi, Alejandro; Bernstein, Jonathan A.; Betschel, Stephen; Bi... Journal: Allergy Issue: Volume 75:Issue 8(2020) Page Start: 2115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Delayed diagnosis of hereditary angioedema with C1‐inhibitor deficiency in iranian children and adolescents. Issue 3 (20th March 2019) Authors: Ayazi, Maryam; Fazlollahi, Mohammad Reza; Mohammadzadeh, Iraj; Fayezi, Abbas; Nabavi, Mohammad; Mahdaviani, Seyed Alireza; Movahedi, Masoud; Heidarzadeh, Marzieh; Saghafi, Shiva; Shokouhi Shoormasti, Raheleh; Mohammadian, Sajedeh; Farkas, Henriette; Pourpak, Zahra Journal: Pediatric allergy and immunology Issue: Volume 30:Issue 3(2019) Page Start: 395 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗