(Q21093254)

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Hereditary thrombophilia

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scholarly article

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Europe PubMed Central

Hereditary thrombophilia (English)

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1 reference

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author name string

Salwa Khan

1

author given names

Salwa

author last names

Khan

1 reference

27 July 2022

Joseph D Dickerman

2

author given names

Joseph D

author last names

Dickerman

1 reference

27 July 2022

language of work or name

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publication date

2006

0 references

Thrombosis journal

1 reference

4

0 references

1

0 references

15

0 references

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Deficiency of protein C in congenital thrombotic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

The nucleotide sequence of the gene for human protein C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Homocysteine lowering and cardiovascular events after acute myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Lipoprotein (a) binds and inactivates tissue factor pathway inhibitor: a novel link between lipoproteins and thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Warfarin induced skin necrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Thrombomodulin gene variations and thromboembolic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism--results of the Spanish Multicentric Study on Thrombophilia (EMET-Study)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

The first mutation identified in the thrombomodulin gene in a 45-year-old man presenting with thromboembolic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 March 2017

Management options for thrombophilias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Genetic thrombophilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

INHERITED ANTITHROMBIN DEFICIENCY CAUSING THROMBOPHILIA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Inherited thrombophilia and venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Pediatric thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Plasminogen activator inhibitor-1 levels and polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Plasminogen and tissue-type plasminogen activator deficiency as risk factors for thromboembolic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Diagnostic studies for thrombophilia in women on hormonal therapy and during pregnancy, and in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Heritable thrombophilia and childhood thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

The influence of platelet collagen receptor polymorphisms in hemostasis and thrombotic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Platelet glycoprotein gene polymorphisms and risk of thrombosis: facts and fancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Venous thrombosis: a multicausal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Age-specific regulation of clotting factor IX gene expression in normal and transgenic mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

World distribution of factor V Leiden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Familial protein S deficiency is associated with recurrent thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

The regulation of hemostasis: the protein C system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Hereditary protein S deficiency: clinical manifestations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Organization of the human protein S genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Abnormal plasminogen. A hereditary molecular abnormality found in a patient with recurrent thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

12 September 2017

Antithrombin Phe229Leu: a new homozygous variant leading to spontaneous antithrombin polymerization in vivo associated with severe childhood thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

27 September 2017

A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

27 September 2017

Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

27 September 2017

Antithrombin III deficiency and thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

27 September 2017

High levels of factor IX increase the risk of venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Factor V Leiden mutation as a risk factor for recurrent pregnancy loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Familial thrombophilia: a complex genetic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Homocysteine and thrombotic disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Apparent different thrombotic tendency in patients with factor V Leiden and protein C deficiency due to selection of patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Vascular pathology of homocysteinemia: implications for the pathogenesis of arteriosclerosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

The clinical spectrum of heterozygous protein C deficiency in a large New England kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

30 May 2018

Complex formation between thrombin and thrombomodulin inhibits both thrombin-catalyzed fibrin formation and factor V activation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 June 2018

The regulation of natural anticoagulant pathways.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

19 June 2018

Homocysteine trials--clear outcomes for complex reasons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

High plasma levels of factor VIII and risk of recurrence of venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Increased plasma levels of lipoprotein(a) and the risk of idiopathic and recurrent venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Fibrinolytic variables in patients with recurrent venous thrombosis: a prospective cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhood.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Is plasminogen deficiency a thrombotic risk factor? A study on 23 thrombophilic patients and their family members.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Clinical features of thrombophilia in families with gene defects in protein C or protein S combined with factor V Leiden.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Factor V and protein S as synergistic cofactors to activated protein C in degradation of factor VIIIa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Prevalence of antithrombin deficiency in the healthy population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592479

29 November 2018

Hereditary heparin cofactor II deficiency and the risk of development of thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the molecular defect in factor VR506Q

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous protein S deficiency: 7-year follow-up

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited thrombophilia: Part 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A database for human fibrinogen variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of 20210 A allele of the prothrombin gene in venous thromboembolism patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation of Arg306 of factor V gene in Hong Kong Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe protein C deficiency in newborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital histidine-rich glycoprotein deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Cambridge: a new mutation (Arg306-->Thr) associated with resistance to activated protein C

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High levels of coagulation factor XI as a risk factor for venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited thrombophilia: Part 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of elevated factor VIII levels in patients referred for thrombophilia screening: role of increased synthesis and relationship to the acute phase reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Therapy with a purified plasminogen concentrate in an infant with ligneous conjunctivitis and homozygous plasminogen deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thromboembolism and bleeding tendency in congenital factor XII deficiency--a study on 74 subjects from 14 Swiss families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clarification of the Risk for Venous Thrombosis Associated with Hereditary Protein S Deficiency by Investigation of a Large Kindred with a Characterized Gene Defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antithrombin III deficiency: decreased synthesis of a biochemically normal molecule

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of a type I quantitative factor V deficiency in a thrombosis patient that is "pseudo homozygous" for activated protein C resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heparin binding properties of human histidine-rich glycoprotein. Mechanism and role in the neutralization of heparin in plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The significance of hypofibrinolysis for the risk of recurrence of venous thromboembolism. Duration of Anticoagulation (DURAC) Trial Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysfibrinogenemia (fibrinogen Dusard) associated with impaired fibrin-enhanced plasminogen activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of Protein S antigen levels in 3788 healthy volunteers: influence of age, sex and hormone use, and estimate for prevalence of deficiency state

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fibrinolytic activity, clotting factors, and long-term incidence of ischaemic heart disease in the Northwick Park Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein S deficiency: a database of mutations--summary of the first update

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital protein C deficiency and venous thromboembolism. A study of three Dutch families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and vascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16968541

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1477-9560-4-15

0 references

Dimensions Publication ID

0 references

0 references

0 references

ResearchGate publication ID

0 references

Sitelinks

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