tallózása szerző szerint "Bork K"

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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 ...
  • International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1-Inhibitor deficiency 
    Farkas, Henriette; Martinez-Saguer I; Bork K; Bowen T; Craig T; Frank M; Germenis AE; Grumach AS; Luczay, Andrea; Varga, Lilian; Zanichelli A; HAWK (2017)
    BACKGROUND: The consensus documents published to date on hereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE) have focused on adult patients. Many of the previous recommendations have not been adapted to pediatric ...