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Advent of oral medications for the treatment of hereditary angioedema.
Valerieva A, Caballero T, Magerl M, Frade JP, Audhya PK, Craig T. Valerieva A, et al. Among authors: caballero t. Clin Transl Allergy. 2024 Sep;14(9):e12391. doi: 10.1002/clt2.12391. Clin Transl Allergy. 2024. PMID: 39331535 Free PMC article. Review.
Determinants of Disease Activity in Adults With Hereditary Angioedema due to C1-Esterase Inhibitor Deficiency.
Lluncor-Salazar M, Phillips-Anglés E, Pedrosa M, Lamacchia D, Hernanz A, Prior N, Cabañas R, Caballero T. Lluncor-Salazar M, et al. Among authors: caballero t. J Investig Allergol Clin Immunol. 2024 Dec 3;34(6):406-409. doi: 10.18176/jiaci.1009. Epub 2024 Jul 26. J Investig Allergol Clin Immunol. 2024. PMID: 39056466 Free article. No abstract available.
Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N-acylethanolamines in patients with hereditary angioedema due to FXII mutation.
Ferrara AL, Palestra F, Piscitelli F, Petraroli A, Suffritti C, Firinu D, López-Lera A, Caballero T, Bork K, Spadaro G, Marone G, Di Marzo V, Bova M, Loffredo S. Ferrara AL, et al. Among authors: caballero t. Allergy. 2024 Jun 27. doi: 10.1111/all.16197. Online ahead of print. Allergy. 2024. PMID: 38935036
The Chronic Angioedema Registry (CARE): Rationale, Methods and Implementation.
Buttgereit T, Aulenbacher F, Gutsche A, Kolkhir P, Weller K, Vera Ayala C, Magerl M, Farkas H, Grumach AS, Aygören-Pürsün E, Bara N, Ben-Shoshan M, Bernstein J, Betschel S, Bouillet L, Caballero T, Cancian M, Castaldo AJ, Cimbollek S, Cohn DM, Craig T, Fomina D, Gelincik A, Grivcheva-Panovska V, Jindal A, Katelaris C, Kessel A, Kinaciyan T, Longhurst HJ, Martinez-Saguer I, Riedl M, Schöffl C, Staubach P, Zanichelli A, Zhi Y, Balle Boysen H, Fok JS, Li PH, Hakl R, Hide M, Peter J, Maurer M. Buttgereit T, et al. Among authors: caballero t. Clin Exp Allergy. 2024 Sep;54(9):712-716. doi: 10.1111/cea.14527. Epub 2024 Jun 24. Clin Exp Allergy. 2024. PMID: 38924594 No abstract available.
Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks.
Riedl MA, Farkas H, Aygören-Pürsün E, Psarros F, Soteres DF, Staevska M, Cancian M, Hagin D, Honda D, Melamed I, Savic S, Stobiecki M, Busse PJ, Dias de Castro E, Agmon-Levin N, Gower R, Kessel A, Kurowski M, Lleonart R, Grivcheva Panovska V, Wedner HJ, Audhya PK, Hao J, Iverson M, Smith MD, Yea CM, Lumry WR, Zanichelli A, Bernstein JA, Maurer M, Cohn DM; KONFIDENT Investigators. Riedl MA, et al. N Engl J Med. 2024 Jul 4;391(1):32-43. doi: 10.1056/NEJMoa2314192. Epub 2024 May 31. N Engl J Med. 2024. PMID: 38819658 Clinical Trial.
Hereditary angioedema in Spain: medical care and patient journey.
Caballero T, Alonso C, Baeza ML, Baynova K, Cabeza J, Cortés I, Escobar Oblitas D, Guilarte M, Joral A, Jurado Palomo J, Lara Jiménez MÁ, Martínez Virto A, Medrano L, Monte Boquet E, Navarro M, Pérez D, Plá Martí MJ, Smith Foltz SL, Suero C, Zamora C. Caballero T, et al. Orphanet J Rare Dis. 2024 May 21;19(1):210. doi: 10.1186/s13023-024-03182-1. Orphanet J Rare Dis. 2024. PMID: 38773490 Free PMC article.
209 results