tallózása szerző szerint "Cicardi M"

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  • Canadian hereditary angioedema guideline. 
    Betschel S; Badiou J; Binkley K; Hebert J; Kanani A; Keith P; Lacuesta G; Yang B; Aygoren-Pursun E; Bernstein J; Bork K; Caballero T; Cicardi M; Craig T; Farkas, Henriette; Longhurst H; Zuraw B; Boysen H; Borici-Mazi R; Bowen T; Dallas K; Dean J; Lang-Robertson K; Laramee B; Leith E; Mace S; McCusker C; Moote B; Poon MC; Ritchie B; Stark D; Sussman G; Waserman S (2014)
    Hereditary angioedema (HAE) is a disease which is associated with random and often unpredictable attacks of painful swelling typically affecting the extremities, bowel mucosa, genitals, face and upper airway. Attacks are ...
  • Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group 
    Cicardi M; Aberer W; Banerji A; Bas M; Bernstein JA; Bork K; Caballero T; Farkas, Henriette; Grumach A; Kaplan AP; Riedl MA; Triggiani M; Zanichelli A; Zuraw B; HAWK; EAACI (2014)
    Angioedema is defined as localized and self-limiting edema of the subcutaneous and submucosal tissue, due to a temporary increase in vascular permeability caused by the release of vasoactive mediator(s). When angioedema ...
  • Recombinant human C1-esterase inhibitor relieves symptoms of hereditary angioedema attacks: Phase 3, randomized, placebo-controlled trial 
    Riedl MA; Bernstein JA; Li H; Reshef A; Lumry W; Moldovan D; Farkas, Henriette; Levy R; Baker J; Hardiman Y; Totoritis MC; Relan A; Cicardi M; on behalf of the Study 1310 Investigators (2014)
    Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is characterized by recurrent attacks of tissue swelling affecting multiple anatomic locations. Recombinant human C1INH ...