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, 1993
The 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
openaire   +2 more sources

C1 Inhibitor Deficiency and Angioedema

2022
Henriette Farkas   +2 more
openaire   +1 more source

C1-inhibitor synthesis by monocytes of patients with C1-inhibitor deficiency

Biochemical Society Transactions, 1987
LINDA JONES   +3 more
openaire   +1 more source

Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency

Journal of Allergy and Clinical Immunology: in Practice, 2017
Andrea Zanichelli   +2 more
exaly  

Autoantibody-Mediated Acquired Deficiency of C1 Inhibitor

New England Journal of Medicine, 1988
J, Jackson, C, Feighery
openaire   +2 more sources

Efficacy of C1 inhibitor concentrate in hereditary angioedema with C1 inhibitor deficiency

Annals of Allergy, Asthma & Immunology, 2018
Aude Belbézier   +4 more
openaire   +1 more source

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency

Allergy: European Journal of Allergy and Clinical Immunology, 2017
Lilian Varga   +2 more
exaly  

[C1 inhibitor deficiency].

Ryoikibetsu shokogun shirizu, 2001
K, Ihara, T, Hara
openaire   +1 more source

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