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Journal Abstract Search
801 related items for PubMed ID: 20143645
1. Treatment of episodes of hereditary angioedema with C1 inhibitor: serial assessment of observed abnormalities of the plasma bradykinin-forming pathway and fibrinolysis. Joseph K, Tholanikunnel TE, Kaplan AP. Ann Allergy Asthma Immunol; 2010 Jan; 104(1):50-4. PubMed ID: 20143645 [Abstract] [Full Text] [Related]
2. Studies of the mechanisms of bradykinin generation in hereditary angioedema plasma. Joseph K, Tuscano TB, Kaplan AP. Ann Allergy Asthma Immunol; 2008 Sep; 101(3):279-86. PubMed ID: 18814451 [Abstract] [Full Text] [Related]
3. Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway. Kaplan AP, Joseph K. Adv Immunol; 2014 Sep; 121():41-89. PubMed ID: 24388213 [Abstract] [Full Text] [Related]
8. Kallikrein-kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys. Bork K, Kleist R, Hardt J, Witzke G. Blood Coagul Fibrinolysis; 2009 Jul; 20(5):325-32. PubMed ID: 19474702 [Abstract] [Full Text] [Related]
9. Diagnosis and treatment of hereditary angioedema. Canonica GW, Rossi O. Panminerva Med; 2012 Sep; 54(3):241-53. PubMed ID: 22801442 [Abstract] [Full Text] [Related]
10. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment. Zeerleder S, Levi M. Ann Med; 2016 Sep; 48(4):256-67. PubMed ID: 27018196 [Abstract] [Full Text] [Related]
13. Factor XII-independent activation of the bradykinin-forming cascade: Implications for the pathogenesis of hereditary angioedema types I and II. Joseph K, Tholanikunnel BG, Bygum A, Ghebrehiwet B, Kaplan AP. J Allergy Clin Immunol; 2013 Aug; 132(2):470-5. PubMed ID: 23672780 [Abstract] [Full Text] [Related]
20. Hereditary angioedema therapies in the United States: movement toward an international treatment consensus. Riedl M. Clin Ther; 2012 Mar; 34(3):623-30. PubMed ID: 22386830 [Abstract] [Full Text] [Related] Page: [Next] [New Search]