… , RE SEDLACK, GJ GLEICH, SJ RUDDY - Annals of Internal …, 1969 - Am Coll Physicians Angioneurotic edema and symptoms of intestinal obstruction developed in a woman when she was 58
years old. Surgical exploration during an attack of abdominal pain showed a segment of jejunum that
was edematous and thickened and had ... Cited by 12 - Related articles - All 2 versions
RP Brettle, RE Dunmow, LA Milne, PL Yap - Scottish medical journal, 1982 - ncbi.nlm.nih.gov A patient presented at the age of 72 years with a life long history of at least 60 years of
abdominal crises described by the patient as 'bilious vomiting or migraine'. However, a careful
clinical and family history ... Cited by 4 - Related articles
KH Krause, U Rentrop, U Mehregan - Journal of the neurological …, 1979 - ncbi.nlm.nih.gov Two patients with hereditary angioneurotic edema are described. A female patient, born in 1929,
showed an infarction in the area of the right posterior cerebral artery, verified by computer
tomography. The son of this ... Cited by 8 - Related articles
T SHINZATO, H NAKAMURA, T KUNIYOSHI, A … - Internal Medicine, 1992 - Journal@rchive An interesting case of hereditary angioedema in a 26-year-old female is reported, with a finding of
transient effusion of fluid into the peritoneal cavity during the attacks. The patient suffered from
recurrent abdominal pain for ... Cited by 9 - Related articles - All 3 versions
J Laurent, MT Guinnepain - Clinical Reviews in Allergy and Immunology, 1999 - Springer Hereditary angioedema was first described by Quincke in 1882 and later by Sir William Osler in 1888
as consisting of recurrent bouts of circumscribed, nonpitting sc edema, primarily of the face,
extremi- ties, upper airway, and ... Cited by 5 - Related articles - BL Direct - All 2 versions
H Farkas, A Csepregi, E Nemesánszky, A Pár, L … - Journal of Allergy and …, 1999 - Elsevier A 58-year-old woman was admitted for evaluation of recurrent, nonpruritic, nonpitting edematous
attacks occurring on the face and upper limbs, which did not affect the airways. These symptoms had
been recurring almost monthly and ... Cited by 14 - Related articles - BL Direct - All 6 versions
- ►kanazawa-u.ac.jp [PDF] H Nomura, Y Tsugawa, I Koni, Y Tofuku, H Mabuchi, … - Internal Medicine, 1992 - Journal@rchive Hereditary angioedema (HAE) is known as a deficiency state of Cl inhibitor (Cl INH), an important
protease inhibitor protein involved in the complement system. As with other components of the
classical pathway of the complement ... Cited by 7 - Related articles - All 4 versions
GW Brasher, JC Starr, FF Hall, AM … - Archives of …, 1975 - archderm.highwire.org Complement component analysis is valuable for differentiating the various types of angioedema.
Patients with hered- itary angioedema have decreased levels of C1 esterase inhibitor and C4 in the
presence of normal amounts of C3 ... Cited by 7 - Related articles - All 4 versions
JS THOMPSON - Annals of Internal Medicine, 1968 - Am Coll Physicians Urticaria may be the sole symptom of a minor reaction or it may be a manifestation of a progressive,
fatal connective tissue or neoplastic disease. At least five basic pathogenetic pathways may
initiate histamine release from ... Cited by 18 - Related articles - All 2 versions
