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Friederike Hauser

Explore the profile of Friederike Hauser including associated specialties, affiliations and a list of published articles. Areas
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Articles 16
Citations 164
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Recent Articles
11.
Barco S, Sollfrank S, Trinchero A, Adenaeuer A, Abolghasemi H, Conti L, et al.
J Thromb Haemost . 2020 Mar; 18(7):1598-1617. PMID: 32202057
Background: Severe plasma prekallikrein (PK) deficiency is an autosomal-recessive defect characterized by isolated activated partial thromboplastin time prolongation. To date, no comprehensive methodologically firm analysis has investigated the diagnostic, clinical,...
12.
Hollerbach A, Muller-Calleja N, Ritter S, Hauser F, Canisius A, Orning C, et al.
Thromb Haemost . 2019 Apr; 119(7):1147-1153. PMID: 31018220
Antiphospholipid antibodies (aPL) have been reported to activate platelets. This is considered to be one of the pathogenic properties of aPL. Even though aPL heterogeneity is quite well established, little...
13.
Darstein F, Hauser F, Straub B, Wenzel J, Conradi R, Mittler J, et al.
Clin Transplant . 2018 Sep; 32(11):e13411. PMID: 30230607
Background: Hepatitis E virus (HEV) infection is a potential reason for elevated liver enzymes after liver transplantation (LT). Our aim was to analyze a real-world cohort of LT patients, who...
14.
Wenzel P, Rossmann H, Muller C, Kossmann S, Oelze M, Schulz A, et al.
Eur Heart J . 2015 Oct; 36(48):3437-46. PMID: 26516175
Aims: Heme oxygenase-1 (HO-1) confers protection to the vasculature and suppresses inflammatory properties of monocytes and macrophages. It is unclear how HO-1 determines the extent of vascular dysfunction in mice...
15.
Prinz N, Hauser F, Lorenz M, Lackner K, von Landenberg P
Immunobiology . 2010 Jul; 216(1-2):145-51. PMID: 20591533
Antiphospholipid antibodies (aPL) are likely involved in the pathogenesis of the antiphospholipid syndrome (APS). This study analyzes the structural and functional characteristics of a human monoclonal aPL (HL7G) from the...
16.
Bickmann J, Kamin W, Wiebel M, Hauser F, Wenzel J, Neukirch C, et al.
Clin Chem . 2009 Apr; 55(6):1083-91. PMID: 19372188
Background: Cystic fibrosis (CF) is a common autosomal recessive genetic disorder caused by a variety of sequence alterations in the CFTR gene [cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family...