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A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process.
J Thromb Haemost. 2019 Nov;17(11):1808-1814. doi: 10.1111/jth.14562. Epub 2019 Jul 22.
J Thromb Haemost. 2019.
PMID: 31271701
Free article.
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.
Morange PE, Peiretti F, Gourhant L, Proust C, Soukarieh O, Pulcrano-Nicolas AS, Saripella GV, Stefanucci L, Lacroix R, Ibrahim-Kosta M, Lemarié CA, Frontini M, Alessi MC, Trégouët DA, Couturaud F.
Morange PE, et al. Among authors: pulcrano nicolas as.
PLoS Genet. 2021 Jan 19;17(1):e1009284. doi: 10.1371/journal.pgen.1009284. eCollection 2021 Jan.
PLoS Genet. 2021.
PMID: 33465109
Free PMC article.
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Whole-Blood miRNA Sequencing Profiling for Vasospasm in Patients With Aneurysmal Subarachnoid Hemorrhage.
Pulcrano-Nicolas AS, Proust C, Clarençon F, Jacquens A, Perret C, Roux M, Shotar E, Thibord F, Puybasset L, Garnier S, Degos V, Trégouët DA.
Pulcrano-Nicolas AS, et al.
Stroke. 2018 Sep;49(9):2220-2223. doi: 10.1161/STROKEAHA.118.021101.
Stroke. 2018.
PMID: 30354977
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Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage.
Pulcrano-Nicolas AS, Jacquens A, Proust C, Clarençon F, Perret C, Shotar E, Puybasset L, Le Goff W, Degos V, Trégouët DA, Garnier S.
Pulcrano-Nicolas AS, et al.
J Neurosurg. 2019 Nov 29:1-5. doi: 10.3171/2019.9.JNS191305. Online ahead of print.
J Neurosurg. 2019.
PMID: 31783362
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