Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.

[1]  S. Cichon,et al.  Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. , 2006, American journal of human genetics.

[2]  K. Bork.  Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations. , 2006, Immunology and allergy clinics of North America.

[3]  K. Bork,et al.  Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. , 2006, Biochemical and biophysical research communications.

[4]  K. Bork,et al.  Hereditary angio‐oedema with normal C1 inhibitor in a family with affected women and men , 2006, The British journal of dermatology.

[5]  K. Bork,et al.  Hereditary angioedema: new findings concerning symptoms, affected organs, and course. , 2006, The American journal of medicine.

[6]  A. Rao,et al.  Erythema Marginatum and Hereditary Angioedema , 2004, Southern medical journal.

[7]  K. Bork,et al.  Hereditary angioedema type III, angioedema associated with angiotensin II receptor antagonists, and female sex. , 2004, The American journal of medicine.

[8]  K. Bork,et al.  Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy. , 2003, The American journal of medicine.

[9]  H. Farkas,et al.  Erythema marginatum preceding an acute oedematous attack of hereditary angioneurotic oedema. , 2001, Acta dermato-venereologica.

[10]  A. Toutain,et al.  Hereditary angioedema type III: an additional French pedigree with autosomal dominant transmission. , 2001, The Journal of allergy and clinical immunology.

[11]  K. Binkley,et al.  Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema. , 2000, The Journal of allergy and clinical immunology.

[12]  K. Bork,et al.  Hereditary angioedema with normal C1-inhibitor activity in women , 2000, The Lancet.

[13]  M. Cicardi,et al.  Hereditary and Acquired C1‐Inhibitor Deficiency: Biological and Clinical Characteristics in 235 Patients , 1992, Medicine.

[14]  D. Stoppa-Lyonnet,et al.  Altered C1 inhibitor genes in type I hereditary angioedema. , 1987, The New England journal of medicine.

[15]  J. Atkinson,et al.  Hereditary angioedema: the clinical syndrome and its management. , 1976, Annals of internal medicine.

[16]  R. R. Evans,et al.  A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE. , 1963, The American journal of medicine.

[17]  R. G. Fraser,et al.  Hereditary cardiovascular dysplasia. A form of familial cardiomyopathy. , 1961, The American journal of medicine.

[18]  W. Osler.  HEREDITARY ANGIO‐NEUROTIC ŒDEMA , 1888 .