Nóra Veszeli

ORCID: 0000-0002-7647-2173 · 2 papers in corpus

observational 2019

Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency

Orphanet journal of rare diseases ·doi:10.1186/s13023-019-0995-7

BACKGROUND AND AIMS: Hereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE) is characterized by localized, non-pitting, and transient swelling of submucosal or subcutaneous region. Human fetuin-A is a multifunctional glycoprotein t…

observational 2016

The effect of long-term danazol treatment on haematological parameters in hereditary angioedema

Orphanet journal of rare diseases ·doi:10.1186/s13023-016-0386-2

BACKGROUND: The 17-alpha-alkylated derivatives of testosterone are often used for the prevention of oedematous episodes in hereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE). However, these agents can have many adverse effects,…