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2019 2
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2023 8
2024 1

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Endothelial Progenitor Cells in Autoimmune Disorders.
Feugray G, Miranda S, Le Cam Duchez V, Bellien J, Billoir P. Feugray G, et al. Stem Cell Rev Rep. 2023 Nov;19(8):2597-2611. doi: 10.1007/s12015-023-10617-y. Epub 2023 Sep 7. Stem Cell Rev Rep. 2023. PMID: 37676423 Review.
Factor XII deficiency evaluated by thrombin generation assay.
Feugray G, Kasonga F, Chamouni P, Barbay V, Fresel M, Hélène Chretien M, Brunel S, Le Cam Duchez V, Billoir P. Feugray G, et al. Clin Biochem. 2022 Feb;100:42-47. doi: 10.1016/j.clinbiochem.2021.11.014. Epub 2021 Nov 26. Clin Biochem. 2022. PMID: 34843733 Clinical Trial.
Afibrinogenemia with two compound heterozygous mutations in FGA gene.
Feugray G, Billoir P, Casini A, Neerman-Arbez M, Barbay V, Chamouni P, Schneider P, Le Cam Duchez V. Feugray G, et al. Haemophilia. 2021 Sep;27(5):e641-e644. doi: 10.1111/hae.14377. Epub 2021 Jul 13. Haemophilia. 2021. PMID: 34255402 No abstract available.
[Acute hemolysis crisis revealed a Wilson disease].
Feugray G, Guillerme J, Fraissinet F, Brunel V, Chagraoui A, Dumant-Forest C, Lahary A. Feugray G, et al. Ann Biol Clin (Paris). 2020 Aug 1;78(4):425-432. doi: 10.1684/abc.2020.1574. Ann Biol Clin (Paris). 2020. PMID: 32618564 Free article. French.
Evaluation of thrombin generation assay in factor XI deficiency.
Kasonga F, Feugray G, Chamouni P, Barbay V, Fresel M, Chretien MH, Brunel S, Le Cam Duchez V, Billoir P. Kasonga F, et al. Among authors: feugray g. Clin Chim Acta. 2021 Dec;523:348-354. doi: 10.1016/j.cca.2021.10.021. Epub 2021 Oct 17. Clin Chim Acta. 2021. PMID: 34670127
22 results