MM Gompels, RJ Lock, M Abinun, CA Bethune, G … - Clinical and experimental Immunology, 2005 - pubmedcentral.nih.gov We present a consensus document on the diagnosis and management of C1 inhibitor
deficiency, a syndrome characterized clinically by recurrent episodes of
angio-oedema. In hereditary angio-oedema, a rare autosomal dominant ... Cited by 104 - Related articles - BL Direct - All 5 versions
R Stasi, D Provan - Mayo Clinic Proceedings, 2004 - mayoclinicproceedings.com From the Department of Medical Sciences, “Regina Apostolorum” Hospital,
Albano Laziale, Italy (RS); and Department of Haematol- ogy, St Bartholomew's
and The Royal London Hospital, London, United Kingdom (DP). Individual ... Cited by 100 - Related articles - View as HTML - BL Direct - All 10 versions
M CICARDI, L BERGAMASCHINI, B MARASINI … - The American Journal of the Medical Sciences, 1982 - journals.lww.com Hereditary Angioedema: An Appraisal of 104 Cases MARCO CICARDI, MD, LUIGI
BERGAMASCHE, MD BIANCA MARASINI, MD GIORGIO BOCCASSINI, MD ANTONIETTA TUCCI, MD
ANGELO AGOSTONI, MD Abstract: One hundred and four patients affected by ... Cited by 68 - Related articles - All 2 versions
- ►bmj.com A Fay, M Abinun - British Medical Journal, 2002 - jcp.bmj.com Hereditary angio-oedema is characterised by recurrent swellings in any part of
the body and also by recurrent attacks of severe abdominal pain. The disease is
inherited in an autosomal dominant manner but up to 25% of cases can occur ... Cited by 40 - Related articles - BL Direct - All 5 versions
L Schneider, W Lumry, A Vegh, AH Williams, … - The Journal of Allergy and Clinical Immunology, 2007 - Elsevier Hereditary angioedema (HAE) is a rare, autosomal-dominant disorder caused by C1
inhibitor gene mutation. Patients with HAE experience intermittent attacks of
edema affecting the oropharynx, abdomen, gastrointestinal tract, and limbs. ... Cited by 34 - Related articles - All 40 versions
- ►haecanada.com [PDF] DE Visentin, WH Yang, J Karsh - Annals of Allergy, Asthma and Immunology, 1998 - ingentaconnect.com INTRODUCTION Quincke 1 reported angioedema in 1882 and Osler 2 described the
hereditary form in 1888. Hereditary angioedema occurs in 1:50,000 to 150,000
people, and accounts for 2% of all cases of angioedema. 3,4 Half of the ... Cited by 32 - Related articles - BL Direct - All 5 versions
A Talavera, JL Larraona, JL Ramos, T López, … - American Journal of Gastroenterology, 1995 - interscience.wiley.com Patients with hereditary angioedema have episodes of local swelling, usually
affecting the face, extremities, upper airway, and gastrointestinal tract. Only
infrequently does it cause recurrent abdominal pain (with or without ... Cited by 32 - Related articles - BL Direct - All 4 versions
J Winnewisser, M Rossi, P Spath, H Burgi - Journal of internal medicine, 1997 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 30 - Related articles - BL Direct - All 4 versions
O Chappatte, M De Swiet - British journal of obstetrics and gynaecology, 1988 - ncbi.nlm.nih.gov 1: Br J Obstet Gynaecol. 1988 Sep;95(9):938-42. Hereditary angioneurotic oedema
and pregnancy. Case reports and review of the literature. ... Cited by 23 - Related articles - All 2 versions
G Széplaki, L Varga, S Valentin, M Kleiber, I … - The Journal of Allergy and Clinical Immunology, 2005 - Elsevier Hereditary angioedema (HAE) is a rare disorder caused by the deficiency of the
C1-inhibitor gene (C1INH). Patients experience recurrent bouts of edema, which
can occur in almost any region of the body. As regards the treatment of the ... Cited by 22 - Related articles - All 16 versions
