Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr)

期刊： HAMOSTASEOLOGIE, 2020; 40 (05)

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

期刊： HAMOSTASEOLOGIE, 2020; 40 (05)

Objective This article aims to analyze the phenotype and genotype of an inherited dysfibrinogenemia pedigree associated with a heterozygous mutation i......

Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family

期刊： HAMOSTASEOLOGIE, 2020; 40 (05)

Objective To study the molecular basis of human coagulation factor XII (FXII) deficiency in a Chinese family. Methods Routine blood coagulation indexe......

IWR-1 Inhibits Collagen-Induced Platelet Activation and Protects against Thrombogenesis

期刊： HAMOSTASEOLOGIE, 2019; 39 (4)

Platelets play a crucial role in haemostasis and several pathophysiological processes. Collagen is a main initiator for platelet activation and aggreg......

JIF：1.0

Congenital hypofibrinogenemia associated with K232T: In vitro expression demonstrates defective secretion of the variant fibrinogen

期刊： HAMOSTASEOLOGIE, 2018; 38 (1)

We have previously reported a case of congenital hypofibrinogenemia caused by a novel heterozygous A -> C transition at nucleotide 5864 of FGG, lea......

JIF：1.0