博士(保健学)信州大学(Shinshu university)Doctoral保健学甲第14号雑誌に発表。THROMBOSIS RESEARCH. 136(6):1318-1324 (2015); doi:10.1016/j.thromres.2015.11.011
We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to...
Congenital afibrinogenemia is a rare coagulopathy characterized by extremely low levels of functiona...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...
Background: We encountered two patients with hypodysfibrinogenemia and designated them as Okayama II...
Background: We encountered two patients with hypodysfibrinogenemia and designated them as Okayama II...
ArticleInternational journal of molecular sciences. 22(10): 5218(2021)journal articl
Congenital hypofibrinogenemia is a rare bleeding disorder characterized by abnormally low levels of ...
A heterozygous patient with dysfibrinogenemia with slight bleeding and no thrombotic complications w...
Background: Inherited fibrinogen deficiencies areclassified into two categories: quantitative, inclu...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Congenital hypofibrinogenaemia is a quantitative fibrinogen disorder characterized by proportionally...
We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to...
We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to...
Congenital afibrinogenemia is a rare coagulopathy characterized by extremely low levels of functiona...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...
Background: We encountered two patients with hypodysfibrinogenemia and designated them as Okayama II...
Background: We encountered two patients with hypodysfibrinogenemia and designated them as Okayama II...
ArticleInternational journal of molecular sciences. 22(10): 5218(2021)journal articl
Congenital hypofibrinogenemia is a rare bleeding disorder characterized by abnormally low levels of ...
A heterozygous patient with dysfibrinogenemia with slight bleeding and no thrombotic complications w...
Background: Inherited fibrinogen deficiencies areclassified into two categories: quantitative, inclu...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while ...
Congenital hypofibrinogenaemia is a quantitative fibrinogen disorder characterized by proportionally...
We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to...
We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to...
Congenital afibrinogenemia is a rare coagulopathy characterized by extremely low levels of functiona...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...