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Publications by Mirko Hirschl
Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
The Risk of Recurrent Venous Thromboembolism in Heterozygous Carriers of Factor v Leiden and a First Spontaneous Venous Thromboembolism
Archives of Internal Medicine
Related publications
Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients
American Journal of Hematology
Hematology
Epidemiology of Prothrombin G20210a Mutation in the Mediterranean Region
Mediterranean Journal of Hematology and Infectious Diseases
Infectious Diseases
Hematology
Type and Location of Venous Thromboembolism in Carriers of Factor v Leiden or Prothrombin G20210A Mutation Versus Patients With No Mutation
Clinical and Applied Thrombosis/Hemostasis
Medicine
Hematology
A C677T Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism and G20210A Mutation in the Prothrombin Gene of Sickle Cell Anemia Patients From Northeast Brazil
Hemoglobin
Biochemistry
Genetics
Clinical Biochemistry
Hematology
Variability of Clinical Manifestation of Factor VII-deficiency in Homozygous and Heterozygous Subjects of the European F7 Gene Mutation A294V
Haematologica
Hematology
Portal Vein Thrombosis Associated to Prothrombin G20210A Mutation and Protein C Deficiency
Clinical and Applied Thrombosis/Hemostasis
Medicine
Hematology
Prevalence and Geographical Variation of Prothrombin G20210A Mutation in Patients With Cerebral Vein Thrombosis: A Systematic Review and Meta-Analysis
PLoS ONE
Multidisciplinary
Loop-Tail Phenotype in Heterozygous Mice and Neural Tube Defects in Homozygous Mice Result From a Nonsense Mutation in the Vangl2 Gene
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Diet-Induced Atherosclerosis in Mice Heterozygous and Homozygous for Apolipoprotein E Gene Disruption.
Journal of Clinical Investigation
Medicine