These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
10. First case of homozygous C1 inhibitor deficiency. Blanch A, Roche O, Urrutia I, Gamboa P, Fontán G, López-Trascasa M. J Allergy Clin Immunol; 2006 Dec; 118(6):1330-5. PubMed ID: 17137866 [Abstract] [Full Text] [Related]
11. Hereditary angioedema in Greek families caused by novel and recurrent mutations. Speletas M, Boukas K, Papadopoulou-Alataki E, Tsitsami E, Germenis AE. Hum Immunol; 2009 Nov; 70(11):925-9. PubMed ID: 19706314 [Abstract] [Full Text] [Related]
16. Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks. Craig TJ, Levy RJ, Wasserman RL, Bewtra AK, Hurewitz D, Obtułowicz K, Reshef A, Ritchie B, Moldovan D, Shirov T, Grivcheva-Panovska V, Kiessling PC, Keinecke HO, Bernstein JA. J Allergy Clin Immunol; 2009 Oct; 124(4):801-8. PubMed ID: 19767078 [Abstract] [Full Text] [Related]
17. Is there a need for clinical guidelines in the United States for the diagnosis of hereditary angioedema and the screening of family members of affected patients? Lunn ML, Santos CB, Craig TJ. Ann Allergy Asthma Immunol; 2010 Mar; 104(3):211-4. PubMed ID: 20377110 [Abstract] [Full Text] [Related]