|1.||Cicardi, Marco: 7 articles (09/2013 - 07/2003)|
|2.||Zanichelli, Andrea: 6 articles (09/2013 - 09/2004)|
|3.||Cicardi, M: 5 articles (05/2015 - 01/2001)|
|4.||Bork, Konrad: 4 articles (08/2014 - 08/2003)|
|5.||Farkas, Henriette: 4 articles (01/2014 - 09/2004)|
|6.||Zanichelli, A: 3 articles (05/2015 - 02/2009)|
|7.||Bernstein, Jonathan A: 3 articles (01/2014 - 08/2002)|
|8.||Cugno, Massimo: 3 articles (09/2013 - 12/2008)|
|9.||Castelli, Roberto: 3 articles (09/2013 - 12/2008)|
|10.||Guilarte, M: 3 articles (01/2011 - 01/2008)|
05/01/1997 - "We have studied 19 patients with hereditary angioedema (HAE) during remission, 5 HAE patients during acute attacks, and 6 patients with acquired angioedema (AAE) during remission and during seven attacks. "
04/01/2015 - "We aimed to study the subgroups of hereditary angioedema with FXII mutation (FXII-HAE), unknown genetic defect (U-HAE) and idiopathic non-histaminergic acquired angioedema (InH-AAE). "
03/01/1995 - "The study included 85 patients with hereditary angioedema and 4 with acquired angioedema. "
03/01/2014 - "In contrast to hereditary angioedema, which usually manifests in childhood, acquired angioedema is broadly recognized to affect people older than 40 years. "
01/01/2014 - "Hereditary angioedema (HAE) and acquired angioedema (AAE) are rare life-threatening conditions caused by deficiency of C1 inhibitor (C1INH). "
05/01/2015 - "According to the new classification of angioedema, the 1058 patients included in this analysis were diagnosed with hereditary (HAE; n = 377) or acquired angioedema (AAE; n = 681). "
05/01/2014 - "Search terms used were: angioedema, HAE, ACE inhibitor induced angioedema, acquired angioedema, type III HAE (now termed HAE with normal C1-INH), diagnosis of HAE, and treatment of HAE. "
01/01/2014 - "Screening for these disorders should occur in all patients with acquired angioedema as treatment may result in resolution of angioedema. "
06/01/2010 - "In patients with recurrent angioedema, the diagnostic classification of the underlying disorder as a particular type of hereditary or acquired angioedema is a prerequisite for appropriate treatment."
06/01/2010 - "Acquired deficiency of C1 inhibitor (C1-INH) with angioedema symptoms (acquired angioedema, AAE) is characterized by local increase in vascular permeability (angioedema) of the skin and the gastrointestinal and oro-pharyngo-laryngeal mucosa. "
11/01/1993 - "These studies led to a diagnosis of hypocomplementemic urticarial vasculitis syndrome, an uncommon to rare form of acquired angioedema, urticarial vasculitis, arthritis, and obstructive airway disease associated with the production of autoantibodies to C1q. "
05/01/2003 - "Others systemic urticaria have been reported without clearly evidence of vasculitis like in primary or acquired angioedema, hereditary periodic fever syndromes and in some thyroiditis. "
|5.||Lymphoproliferative Disorders (Lymphoproliferative Disorder)
08/15/2002 - "As with type 1 disease, a large proportion of patients with acquired angioedema type 2 have a lymphoproliferative disorder."
04/01/1997 - "Acquired angioedema (AAE) is a rare disorder that has been categorized into two forms, AAE-I and AAE-II. AAE-I is associated with other diseases, most commonly B-cell lymphoproliferative disorders. "
12/01/1993 - "Acquired angioedema as the presenting feature of lymphoproliferative disorders of mature B-lymphocytes."
10/01/2011 - "Acquired angioedema (AAE) with C1 inhibitor deficiency is often associated to B cell lymphoproliferative disorders or autoimmune diseases. "
01/01/2014 - "Acquired angioedema is a rare but recognized manifestation of lymphoproliferative disorders due to deficiency in C1 esterase inhibitor. "
|2.||Complement C1 Inhibitor Protein (C1 Esterase Inhibitor)
|4.||Complement System Proteins (Complement)
|5.||Angiotensin-Converting Enzyme Inhibitors (ACE Inhibitors)
|7.||Peptidyl-Dipeptidase A (Angiotensin Converting Enzyme)
|10.||factor V Leiden
|1.||Hormone Replacement Therapy (Therapy, Hormone Replacement)
|3.||Drug Therapy (Chemotherapy)