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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.
[Bloody tears: About a case and a review of the literature].
Billoir P, Feugray G, Chrétien MH 5th, Fresel M, Le Cam Duchez V. Billoir P, et al. Among authors: feugray g. Rev Med Interne. 2020 May;41(5):339-342. doi: 10.1016/j.revmed.2019.12.007. Epub 2019 Dec 24. Rev Med Interne. 2020. PMID: 31882188 Review. French.
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.
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
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.
25 results