Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency Bernadett Márkus, Nóra Veszeli, György Temesszentandrási, Henriette Farkas and László Kalabay Orphanet Journal of Rare Diseases 2019, 14:67 | Published on: 18 March 2019 Full Text | PDF

Follow BMC on: . For further information or enquiries please use our contact page details. BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy. BioMed Central Ltd The Campus, 4 Crinan Street, London, N1 9XW, United Kingdom

© 2019 BioMed Central Limited unless otherwise stated. Part of Springer Nature.