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Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.
Thromb Res. 2011 Sep;128(3):233-6. doi: 10.1016/j.thromres.2011.03.024. Epub 2011 Apr 16.
Thromb Res. 2011.
PMID: 21497883
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship.
Tiscia GL, Favuzzi G, Lupone MR, Cappucci F, Schiavulli M, Mirabelli V, D'Andrea G, Chinni E, Giuliani N, Caliandro R, Grandone E.
Tiscia GL, et al. Among authors: lupone mr.
Hum Genome Var. 2017 Nov 9;4:17043. doi: 10.1038/hgv.2017.43. eCollection 2017.
Hum Genome Var. 2017.
PMID: 29138690
Free PMC article.
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Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.
D'Andrea G, Bossone A, Lupone MR, Peyvandi F, Maisto G, Perricone F, Grandone E, Margaglione M.
D'Andrea G, et al. Among authors: lupone mr.
Haematologica. 2004 Aug;89(8):979-84.
Haematologica. 2004.
PMID: 15339682
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A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.
Margaglione M, Santacroce R, Colaizzo D, Seripa D, Vecchione G, Lupone MR, De Lucia D, Fortina P, Grandone E, Perricone C, Di Minno G.
Margaglione M, et al. Among authors: lupone mr.
Blood. 2000 Oct 1;96(7):2501-5.
Blood. 2000.
PMID: 11001903
Free article.
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The prothrombin time/international normalized ratio (PT/INR) Line: derivation of local INR with commercial thromboplastins and coagulometers--two independent studies.
Poller L, Ibrahim S, Keown M, Pattison A, Jespersen J; European Action On Anticoagulation.
Poller L, et al.
J Thromb Haemost. 2011 Jan;9(1):140-8. doi: 10.1111/j.1538-7836.2010.04109.x.
J Thromb Haemost. 2011.
PMID: 20942851
Free article.
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