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Search: authors:"Katarina Bremme"

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Blood inflammatory and endothelial markers in women with von Willebrand disease

Conceptualization: Katarina Bremme, Margareta Holmstro?m, Miriam Mints. Data curation: Igor Govorov, Roza Chaireti. Formal analysis: Igor Govorov, Roza Chaireti. Investigation: Anders Larsson, Eduard Komlichenko ... , Roza Chaireti. Methodology: Katarina Bremme, Anders Larsson, Margareta Holmstro?m, Roza Chaireti, Miriam Mints. 7 / 10 Project administration: Miriam Mints. Resources: Miriam Mints. Software: Igor

Thrombin generation during a regular menstrual cycle in women with von Willebrand disease

Fluctuations of the sex steroids during the menstrual cycle might significantly influence hemostasis. This association, derived from a number of the observations on healthy women, is yet to be described in females affected by bleeding disorders. The aim of the current study was to assess the changes in hemostatic variables in women with vWD during two phases of the menstrual...

Postpartum Hemorrhage in Women with Von Willebrand Disease – A Retrospective Observational Study

Introduction von Willebrand disease (VWD) is a hereditary bleeding disorder, caused by a deficiency in the levels and/or function of von Willebrand factor (VWF). Women with VWD appear to be at increased risk of experiencing postpartum hemorrhage (PPH), though the levels of VWF increase during pregnancy. There is limited knowledge of how PPH is associated with the subtype of VWD...

Normalized endothelial function but sustained cardiovascular risk profile 11 years following a pregnancy complicated by preeclampsia

Anders Larsson in:Nature Research journals • PubMed • Google ScholarSearch for Maria Eriksson in:Nature Research journals • PubMed • Google ScholarSearch for Katarina Bremme in:Nature Research journals

The histidine-rich glycoprotein A1042G polymorphism and recurrent miscarriage: a pilot study

Background Histidine-rich Glycoprotein (HRG) has previously been shown to have an impact on implantation and fertility. The aim of this study was to investigate if there is an association between the HRG A1042G single nucleotide polymorphism (SNP) and recurrent miscarriage. Methods The study was designed as a case-control study and the women were included at University Hospitals...

Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: A retrospective case control study

Background Recurrent miscarriage affects approximately 1% of all couples. There is a known relation between hypothyroidism and recurrent miscarriage. Phosphodiesterase 8B (PDE8B) is a regulator of cyclic adenosine monophosphate (cAMP) with important influence on human thyroid metabolism. Single nucleotide polymorphism (SNP) rs 4704397 in the PDE8B gene has been shown to be...