Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study-Reference-Cited by-同舟云学术

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study

Published:2017-12 Issue:8 Volume:28 Page:623-626
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Girolami Antonio,Santarossa Claudia,Cosi Elisabetta,Ferrari Silvia,Lombardi Anna Maria,Girolami Bruno

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

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4. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias;Acharya;J Thromb Haemost,2004

5. Rare quantitative and qualitative abnormalities of coagulation;Girolami;Clin Haematol,1985

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