Results 111 to 120 of about 557 (197)

Hereditary angioedema in childhood [PDF]

Clinical and Experimental Pediatrics, 2020
openaire   +3 more sources

Selection of initiatives to improve the management of patients with hereditary angioedema by the hospital pharmacy using the nominal group technique. [PDF]

Eur J Hosp Pharm
Montoro Ronsano JB, Martínez Sesmero JM, Cortés I, Lleonart R.   +3 more
europepmc   +1 more source

Probiotic supplementation to mitigate berotralstat gastrointestinal side effects: a multicenter case series from the ITACA network. [PDF]

Front Immunol
Gidaro A, Guarino MD, Arcoleo F, Bignardi D, D'Antonio C, Brussino L, Accardo P, Nicola S, Pucci S, Cognigni M, Popescu Janu V, Cogliati C, Bizzi E, Cancian M.   +13 more
europepmc   +1 more source

Hereditary Angioedema Prophylaxis Therapy: Berotralstat and Lanadelumab Safety Profile. [PDF]

Medicina (Kaunas)
Donadoni M, La Cava L, Bizzi E, Popescu Janu V, Meschia A, Cirigliano F, Cogliati C, Gidaro A.   +7 more
europepmc   +1 more source

Acquired angioedema due to C1 inhibitor deficiency: real-world clinical characteristics and treatment outcomes. [PDF]

Front Immunol
Toprak İD, Erdem S, Korkmaz P, Unal D, Yegit OO, Hormet Igde M, Çelik Kamacı Ş, Çetin O, Öztop N, Demir S, Tüzer C, Mastanzade M, Elverdi T, Sezgin ME, Kalayoğlu Beşışık S, Gelincik A.   +15 more
europepmc   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Comparative Efficacy of Recombinant C1 Inhibitor Versus Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks: A Matching-Adjusted Indirect Treatment Comparison. [PDF]

Adv Ther
Anderson J, Narsipur N, Jones D, Smith A, Relan A, Aiello E, Roskell N, Gough A, Jindal S, Habimana K, Kilvert H, Li HH, Harrington A.   +12 more
europepmc   +1 more source

Hereditary angioedema: An update

Indian Journal of Dermatology, Venereology, and Leprology, 2011
openaire   +2 more sources

Recurrent angioedema manifestation and treatment response in two patients from different families caring the myoferlin gene mutation: case series. [PDF]

Orphanet J Rare Dis
Fomina DS, Lebedkina MS, Bobrikova EN, Yukhnovskaya YD, Roppelt AA, Mukhina OA, Markina UA, Alexeeva YG, Nikitina EA, Maurer M, Karaulov AV, Lysenko MA, Buttgereit T.   +12 more
europepmc   +1 more source

Burden of hereditary angioedema: results from a multinational survey of caregivers for adult and pediatric patients. [PDF]

Orphanet J Rare Dis
Watt M, Martinez-Saguer I, Simon A, Murphy R, De La Cruz M, Zwiener R, Sarrazola M, Grumach AS.   +7 more
europepmc   +1 more source