Results 61 to 70 of about 499 (149)

Unraveling angioedema: diagnostic challenges and emerging therapies. [PDF]

Front Immunol
Johnson F, Hofauer B.
europepmc   +1 more source

Pain management in patients with hereditary angioedema: A case report. [PDF]

Medicine (Baltimore)
Li X, Ran Y, Zuo C, He S, Ma Y, Li X.
europepmc   +1 more source

Hereditary angioedema

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 1997
Vasiliki Karlis, Robert S Glickman, Richard Stern, Lisa Kinney   +3 more
openaire   +3 more sources

Patient-reported disease burden and health care utilization of HAE-nl-C1INH: insights from a real-world survey. [PDF]

Clin Exp Med
Jones D, Narsipur N, Wade SW, Harper JR, Park N, Adams P, Relan A, Harrington A, Anderson J.   +8 more
europepmc   +1 more source

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

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

Management of hereditary angioedema with normal C1Inh: a series of 163 French patients. [PDF]

Orphanet J Rare Dis
Bocquet A, Bouillet L, Hardy G, Boccon-Gibod I, Deroux A, Arnaud M, Pelletier F, Thanh AD, Ozanne N, Armengol G, Jeandel PY, Sailler L, Taquet MC, Launay D, Fain O, Gobert D.   +15 more
europepmc   +1 more source

Hereditary Angioedema

Zdorovʹe Rebenka, 2014
Наследственный ангионевротический отек — редкое заболевание, обусловленное врожденным дефицитом С1-ингибитора. Клинические проявления заболевания — рецидивирующие эпизоды ангионевротического отека, которые манифестируют в детском или подростковом возрасте, чаще всего локализуются в подкожной клетчатке (конечности, лицо, туловище, половые органы) или в ...
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

Hereditary Angioedema

Journal of Investigative Dermatology, 1973
openaire   +2 more sources