- ►annals.org [PDF] SN Markovic, DJ Inwards, RP Phyliky - Annals of internal medicine, 2000 - Am Coll Physicians The Editors welcome submissions for possible publication in the Letters section.
Authors of letters should: • Include no more than 300 words of text, three
authors, and five references • Type with double-spacing • Send three ... Cited by 95 - Related articles - BL Direct - All 7 versions
M Cicardi, G Bisiani, M Cugno, P Spath, A … - The American Journal of Medicine, 1993 - Elsevier Four patients with AAE had no other diseases, one had breast cancer, one liver
hydatidosis, one Waldenstrom's disease, and one a benign M component. Functional
C1-INH levels were below 30% of normal, and Clq plasma levels were low in ... Cited by 38 - Related articles - BL Direct - All 3 versions
NF Jensen, JM Weiler - Anesth Analg, 1998 - anesthanalg.com H ereditary angioedema (HAE) is a serious genetic abnormality involving the
complement system and characterized by episodic and sometimes life-threatening
airway edema. In 1882, von Quincke (1) published the first detailed ... Cited by 40 - Related articles - View as HTML - BL Direct - All 12 versions
WR Heymann - Journal of the American Academy of Dermatology, 1997 - Elsevier Angioedema (formerly called angioneurotic edema) was first described by Quincke
1 in 1882 and is characterized by painless, nonpruritic swelling of the skin. In
1888 Osler 2 offered the first complete depiction of hereditary angioedema ... Cited by 40 - Related articles - BL Direct - All 3 versions
M D'Incan, A Tridon, D Ponard, C Dumestre- … - Dermatology, 2000 - content.karger.com Angioedema is clinically characterized by the recurrence of sudden attacks of
subcutaneous and/or mucosal edemas. Involvement of the upper respiratory tract
may have a fatal outcome and involvement of the gastrointestinal tract may ... Cited by 22 - Related articles - BL Direct - All 5 versions
J Jackson, RB Sim, A Whelan, C Feighery, 1986 - nature.com Antibodies are considered to play a specific pathogenic role in certain disease
states such as myasthenia gravis, Graves' disease and autoimmune haemolytic
anaemia 1−3 . Autoantibodies which interfere with the function of enzyme ... Cited by 76 - Related articles - All 4 versions
J Alsenz, K Bork, M Loos - New England Journal of Medicine, 1987 - content.nejm.org During the past 25 years, three forms of deficiency of the inhibitor of the
first component of complement (C1 inhibitor) with angioedema have been
recognized; two forms are hereditary and one is acquired. As compared with ... Cited by 97 - Related articles - All 3 versions
UC Nzeako, E Frigas, WJ Tremaine - Archives of Internal Medicine, 2001 - archinte.highwire.org Hereditary angioedema (HAE) is an autosomal dominant disease that afflicts 1 in
10 000 to 1 in 150 000 persons; HAE has been reported in all races, and no sex
predominance has been found. It manifests as recurrent attacks of intense, ... Cited by 117 - Related articles - BL Direct - All 4 versions
A Chevailler, G Arlaud, D Ponard, M Pernollet, … - Journal of Allergy and Clinical Immunology, 1996 - Elsevier The syndrome of acquired angioneurotic edema (AAE) is characterized by the adult
onset of angioedema, the lack of evidence for inheritance of the disorder, and
the frequent association of the C1-inhibitor (C1-INH) deficiency with ... Cited by 23 - Related articles - BL Direct - All 3 versions
M Cicardi, A Beretta, M Colombo, D Gioffre, … - Clinical and Experimental Immunology, 1996 - interscience.wiley.com We looked for autoantibodies to C1 inhibitor (C1-INH) and evaluated the
relationship of their presence to the associated lymphoproliferative diseases
and to the cleaved form of C1-INH in 13 patients with acquired C1-INH ... Cited by 45 - Related articles - BL Direct - All 5 versions
