(Q34340628)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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1 reference

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author name string

Girolami A

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Randi ML

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Gavasso S

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Lombardi AM

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Spiezia F

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 April 2004

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Journal of Thrombosis and Thrombolysis

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Europe PubMed Central

PubMed publication ID

1 August 2017

17

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Europe PubMed Central

PubMed publication ID

1 August 2017

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

139-143

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Europe PubMed Central

PubMed publication ID

1 August 2017

Cholecystectomy in a patient with Hageman trait

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations of factor XII level during pregnancy in a woman with Hageman factor deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. luscaber@tin.it

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Williams trait. Human kininogen deficiency with diminished levels of plasminogen proactivator and prekallikrein associated with abnormalities of the Hageman factor-dependent pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombophilia with a combination of antithrombin III and factor XII deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

World distribution of factor V Leiden

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor XII clotting activity and antigen levels in patients with thromboembolic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent thrombosis in a young woman with a circulating anticoagulant directed against factors XI and XII

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Should factor XII assays be included in thrombophilia screening?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Geographic distribution of the 20210 G to A prothrombin variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

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/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital deficiency of Hageman factor (clotting factor XII). Report on the first two families found in Switzerland

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superficial migratory thrombophlebitis and factor XII deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent thrombosis in a patient with factor XII deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arterial and venous thrombosis and normal response to streptokinase treatment in a young patient with severe Hageman factor deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor XII deficiency and central retinal vein occlusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombophlebitis and pulmonary embolism in congenital factor XII deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombosis in patients with heterozygous and homozygous factor XII deficiency is not explained by the associated presence of factor V Leiden

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple cerebral thrombosis in Fletcher factor (prekallikrein) deficiency: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

John Hageman's factor and deep-vein thrombosis: Leiden thrombophilia Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced Titers of Hageman Factor (Factor XII) in Orientals

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombosis in subjects with homozygous and heterozygous factor XII deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Factor XII (Hageman factor) deficiency: a risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboembolism and myocardial infarction]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor XII deficiency and pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additional factor XII (Hageman factor) deficiency in hemophilia A and in von Willebrand syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rarer quantitative and qualitative abnormalities of coagulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The behavior of the blood platelets in hemorrhagic diseases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absent plasma second phase platelet aggregation factor in a patient with Hageman trait

1 reference

https://pubmed.ncbi.nlm.nih.gov/15306750

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/B:THRO.0000037670.42776.CD

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

release_2ezuc2satndqrjelud2d6y6mze

1 reference

https://api.fatcat.wiki/v0/release/2ezuc2satndqrjelud2d6y6mze

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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