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Mingshan Wang

First Affiliated Hospital of Wenzhou Medical University

47

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Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency.

2021 Acta Haematologica
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Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene

2020 Hamostaseologie
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Fabricating antimicrobial peptide-immobilized starch sponges for hemorrhage control and antibacterial treatment

2019 Carbohydrate Polymers
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Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiency

2019 Hematology
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Poly(lactide-co-glycolide) grafted hyaluronic acid-based electrospun fibrous hemostatic fragments as a sustainable anti-infection and immunoregulation material

2019 Journal of Materials Chemistry B
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Two Novel Mutations Cause Hereditary Antithrombin Deficiency in a Chinese Family

2019 Acta Haematologica
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Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene

2019 Chinese journal of medical genetics
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Clinical and molecular characterization of nine Chinese patients affected by hypofibrinogenemia or dysfibrinogenemia

2018 Blood Coagulation & Fibrinolysis
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Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis

2018 Blood Coagulation & Fibrinolysis
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Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene

2018 Chinese journal of medical genetics
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