K. Wulff
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View article: Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin
Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin Open
Hereditary angioedema (HAE) is characterized by recurrent localized edema in various organs, which can be potentially fatal. There are different types of hereditary angioedema, which include genetic deficiency of C1 inhibitor (C1-INH) and …
View article: Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence Open
Background Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH) (HAEnCI) is associated with skin swellings, abdominal attacks, and the risk of asphyxia due to upper airway obstruction. Several different gene mutations linked to th…
View article: Hereditäres Angioödem in einer Familie mit spezifischen Mutationen sowohl im Plasminogen‐ als auch im SERPING1‐Gen
Hereditäres Angioödem in einer Familie mit spezifischen Mutationen sowohl im Plasminogen‐ als auch im SERPING1‐Gen Open
Zusammenfassung Hintergrund Die Bezeichnung hereditäres Angioödem (HAE) steht für eine Gruppe genetischer Erkrankungen mit rezidivierenden, schmerzhaften und potenziell lebensbedrohlichen Gewebeschwellungen. Die häufigste Variante des HAE …
View article: Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene
Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene Open
View article: Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes
Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes Open
Summary Background Hereditary angioedema (HAE) is a group of genetic diseases characterized by recurrent, painful and potentially lethal tissue swelling. The most common form results from mutations in the SERPING1 gene, leading to reduced …
View article: Treatment of Hereditary Angioedema with the Mutation c.988A>G (p.K330E) in the Plasminogen Gene
Treatment of Hereditary Angioedema with the Mutation c.988A>G (p.K330E) in the Plasminogen Gene Open
View article: Severe Tongue Swellings In Hereditary Angioedema With A Specific Mutation In The Plasminogen Gene
Severe Tongue Swellings In Hereditary Angioedema With A Specific Mutation In The Plasminogen Gene Open
View article: Tamoxifen, a Trigger Factor of Hereditary Angioedema with Normal C1-INH with a Specific Mutation in the F12 Gene (HAE-FXII)
Tamoxifen, a Trigger Factor of Hereditary Angioedema with Normal C1-INH with a Specific Mutation in the F12 Gene (HAE-FXII) Open