Results 241 to 250 of about 1,197,187 (269)
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Clinical problems in the C1-inhibitor deficient patient.
Behring Institute Mitteilungen, 1993The clinical course of C1-INH deficiency is presently well established. There is an inherited form (Hereditary Angioedema) characterized by recurrence of cutaneous and mucous swellings appearing early in life and usually accompanied by substantial family history, and an acquired form (Acquired Angioedema) where identical symptoms start after the fourth
A. Agostoni +3 more
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C1-inhibitor synthesis by monocytes of patients with C1-inhibitor deficiency
Biochemical Society Transactions, 1987LINDA JONES +3 more
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Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency
Journal of Allergy and Clinical Immunology: in Practice, 2017Andrea Zanichelli +2 more
exaly
Autoantibody-Mediated Acquired Deficiency of C1 Inhibitor
New England Journal of Medicine, 1988J, Jackson, C, Feighery
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Efficacy of C1 inhibitor concentrate in hereditary angioedema with C1 inhibitor deficiency
Annals of Allergy, Asthma & Immunology, 2018Aude Belbézier +4 more
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