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Genetic test indications and interpretations in patients with hereditary angioedema.
Weiler CR, van Dellen RG. Weiler CR, et al. Mayo Clin Proc. 2006 Jul;81(7):958-72. doi: 10.4065/81.7.958. Mayo Clin Proc. 2006. PMID: 16835976 Review.
Patients with hereditary angioedema (HAE) present with recurrent, circumscribed, and self-limiting episodes of tissue or mucous membrane swelling caused by C1-inhibitor (CI-INH) deficiency. The estimated frequency of HAE is 1:50,000 persons. Distinguishing HAE from …
Patients with hereditary angioedema (HAE) present with recurrent, circumscribed, and self-limiting episodes of tissue or mucous membrane swe …
Familial occurrence of C1-inhibitor deficiency and the effect of treatment.
Madaliński K, Sabbouh K, Imielska D, Chorazykiewicz M. Madaliński K, et al. Arch Immunol Ther Exp (Warsz). 1989;37(5-6):669-74. Arch Immunol Ther Exp (Warsz). 1989. PMID: 2487375
The results of complement determination in these patients (5 girls and 1 mother) were compared to the rest of the group and to healthy blood donors and showed clear differences in concentrations of C1-inhibitor, C1q, C4 and in haemolytic activity. Treatment consiste …
The results of complement determination in these patients (5 girls and 1 mother) were compared to the rest of the group and to health …
Treatment of AB deficiencies.
Cunningham-Rundles C. Cunningham-Rundles C. Vox Sang. 1986;51 Suppl 2:63-8. doi: 10.1111/j.1423-0410.1986.tb02010.x. Vox Sang. 1986. PMID: 3490056
The objective of this study was to compare serum immunoglobulin levels and the clinical status of patients with primary immune deficiency who received an intravenous immunoglobulin (IVIG) (pH 4.0) preparation for 1 year with results previously obtained when the same …
The objective of this study was to compare serum immunoglobulin levels and the clinical status of patients with primary immune deficiency