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A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIII Dorgalaleh, Akbar; Tabibian, Shadi; Shams, Mahmood; Majid, Golbahar; ... Safa, Majid 2019
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Scoring Systems for Diagnosis of Acute Venous Thromboembolism Le Gal, Grégoire; Righini, Marc Philip; Wells, Philip S 2017
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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite 2016
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Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro 2016
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Congenital fibrinogen disorders: an update De Moerloose, Philippe; Casini, Alessandro; Neerman Arbez, Marguerite 2013
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Fibrinogen and the risk of thrombosis De Moerloose, Philippe; Boehlen, Françoise; Neerman Arbez, Marguerite 2010
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Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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Technical aspects in laboratory testing for antiphospholipid antibodies: is standardization an impossible dream? Reber, Guido; Boehlen, Françoise; De Moerloose, Philippe 2008