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Ulrike Nowak-Göttl

University of Münster
Boston Children's Hospital

350

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Acquired von Willebrand syndrome in ECMO patients: A 3-year cohort study

2021 Blood Cells Molecules and Diseases
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Genotype-Phenotype Relationship Among 1200 Unrelated White Patients with Inherited FVII Deficiency: A Three-Center Database Study

2021 Blood
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Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.

2021 Thrombosis and Haemostasis
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International pediatric thrombosis network to advance pediatric thrombosis research: Communication from the ISTH SSC subcommittee on pediatric and neonatal thrombosis and hemostasis.

2021 Journal of Thrombosis and Haemostasis
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Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia

2020 Acta Haematologica
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Cross-Sectional and Longitudinal Construct Validity of the Generic KINDL-A(dult)B(rief) Questionnaire in Adults with Thrombophilia or with Hereditary and Acquired Bleeding Disorders.

2020 Acta Haematologica
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Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study.

2020 Journal of Thrombosis and Thrombolysis
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Genome-wide analysis of 944,133 individuals provides insights into the etiology of hemorrhoidal disease

2020 medRxiv
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Replacement Therapy in Patients with Von Willebrand Disease—Indications and Monitoring

2019 Hamostaseologie
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Recurrent stroke: the role of thrombophilia in a large international pediatric stroke population

2019 Haematologica
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Citations (11)