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Showing 1 to 8 of 8 for “"C1-inhibitor"”.

  1. Biokompatibilitätsuntersuchungen an Originaldialysatoren in einem In-vitro-Dialyse-Rezirkulationsmodell unter besonderer Berücksichtigung von Faktor XIIa-C1-Inhibitor, einem Marker für die Aktivierung des Kontaktphasensystems

    … a newly developed immunoassay for factor XIIa-C1-inhibitor complex.Results: With blood from healthy volunteers there was no difference in thrombogenicity between Cuprophan® and Polysulfone. Cuprophan® caused a much stronger complement activation than Polysulfone.Only in-vitro dialysis with the …

    aachen Repository record for Biokompatibilitätsuntersuchungen an Originaldialysatoren in einem In-vitro-Dialyse-Rezirkulationsmodell unter besonderer Berücksichtigung von Faktor XIIa-C1-Inhibitor, einem Marker für die Aktivierung des Kontaktphasensystems (opens in a new tab)

  2. ¿PLASMA LEVELS OF BRADYKININ AND CLEAVED HIGH MOLECULAR WEIGHT KININOGEN IN PATIENTS WITH IDIOPATHIC ANGIOEDEMA DURING ACUTE ATTACK¿

    … drug-induced or due to an acquired C1-inhibitor deficiency; however, several cases remain idiopathic. The role of bradykinin in increasing vascular permeability has been demonstrated in angioedema due to C1-inhibitor deficiency and in angioedema due to the treatment with angiotensin …

    milano Repository record for ¿PLASMA LEVELS OF BRADYKININ AND CLEAVED HIGH MOLECULAR WEIGHT KININOGEN IN PATIENTS WITH IDIOPATHIC ANGIOEDEMA DURING ACUTE ATTACK¿ (opens in a new tab)

  3. Molekulare Ursachen des hereditären Angioödems

    Mutationen im C1-Inhibitor(C1-INH)-Gen manifestieren sich in Form autosomal dominant vererbter Angioödeme (hereditäres Angioödem (HAE)), wobei zwei Typen unterschieden werden. Während der HAE-Typ I mit einer Häufigkeit von 85% auftritt und durch erniedrigte C1-INH-Plasmaspiegel mit daraus …

    wurz-thes Repository record for Molekulare Ursachen des hereditären Angioödems (opens in a new tab)

  4. Angioedema Ereditario: aspetti neurobiologici e strategie di coping

    … that prevents the formation of a protein called C1 inhibitor, essential for the human’s life, is the base of pathology known as “Hereditary Angioedema” (HAE). This pathology involves the onset of acute attacks consisting of circumscribed edema of the mucous membranes and of the subcutaneous. An …

    catania Repository record for Angioedema Ereditario: aspetti neurobiologici e strategie di coping (opens in a new tab)

  5. Zur Frage der Aktivierung des Gerinnungs- und Komplementsystemes bei Verwendung von oberflächenmodifizierten Biomaterialien

    … Significantly increased binding of complement inhibitors C1 Inhibitor and factor H on HBS lead to significantly reduced detection of activation specific complement proteins (iC3b and C5b-9) demonstrating reduced complement activation. Analysis of alternative C3-convertase and soluble terminal …

    aachen Repository record for Zur Frage der Aktivierung des Gerinnungs- und Komplementsystemes bei Verwendung von oberflächenmodifizierten Biomaterialien (opens in a new tab)