Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.

Haisma B, Nieuwenstein T, Rijpma SR, Simons A, Blijlevens NMA, van Heerde WL, Schols SEM

Open source

DOI
10.1016/j.rpth.2026.106928
Published
2026 Aug
Container
Research and practice in thrombosis and haemostasis
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.rpth.2026.106928,
  title = {Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.},
  author = {Haisma B and Nieuwenstein T and Rijpma SR and Simons A and Blijlevens NMA and van Heerde WL and Schols SEM},
  year = {2026},
  journal = {Research and practice in thrombosis and haemostasis},
  doi = {10.1016/j.rpth.2026.106928},
  url = {https://doi.org/10.1016/j.rpth.2026.106928}
}

RIS

TY  - JOUR
TI  - Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.
AU  - Haisma B
AU  - Nieuwenstein T
AU  - Rijpma SR
AU  - Simons A
AU  - Blijlevens NMA
AU  - van Heerde WL
AU  - Schols SEM
PY  - 2026
JO  - Research and practice in thrombosis and haemostasis
DO  - 10.1016/j.rpth.2026.106928
UR  - https://doi.org/10.1016/j.rpth.2026.106928
ER  - 

APA

B, H., T, N., SR, R., A, S., NMA, B., WL, V. H., & SEM, S. (2026). Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.. Research and practice in thrombosis and haemostasis. https://doi.org/10.1016/j.rpth.2026.106928

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