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Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.
Adenaeuer A, Barco S, Trinchero A, Krutmann S, Nazir HF, Ambaglio C, Rocco V, Pancione Y, Tomao L, Ruiz-Sáez A, Echenagucia M, Alesci S, Sollfrank S, Ezigbo ED, Häuser F, Lackner KJ, Lämmle B, Rossmann H. Adenaeuer A, et al. Among authors: trinchero a. J Thromb Haemost. 2023 Feb;21(2):237-254. doi: 10.1016/j.jtha.2022.11.011. Epub 2022 Dec 22. J Thromb Haemost. 2023. PMID: 36700498 Free article.
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC.
Gresele P, Orsini S, Noris P, Falcinelli E, Alessi MC, Bury L, Borhany M, Santoro C, Glembotsky AC, Cid AR, Tosetto A, De Candia E, Fontana P, Guglielmini G, Pecci A; BAT-VAL study investigators. Gresele P, et al. J Thromb Haemost. 2020 Mar;18(3):732-739. doi: 10.1111/jth.14683. Epub 2019 Dec 16. J Thromb Haemost. 2020. PMID: 31750621 Free article.
Safety of prothrombin complex concentrate in healthy subjects.
Barco S, Picchi C, Trinchero A, Middeldorp S, Coppens M. Barco S, et al. Among authors: trinchero a. Br J Haematol. 2017 Feb;176(4):664-666. doi: 10.1111/bjh.13974. Epub 2016 Mar 30. Br J Haematol. 2017. PMID: 27027385 Free article. No abstract available.
38 results