Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The Saudi Thrombosis and Familial Thrombophilia Registry. Design, rational, and preliminary results.

Saudi medical journal - 1 Oct 2009

Saour Jalal N, Shoukri Mohammed M, Mammo Layla A

Abstract excerpt

OBJECTIVE: To describe the Registry and report preliminary data for the prevalence of 5 prothrombotic gene mutations in the normal Saudi population. METHODS: Blood from consenting healthy Saudi individuals and patients with venous thrombosis (VT) from different regions of the Kingdom was collected from November 2001 until July 2007. The extracted DNA of each sample was kept at -70 degrees C until tested for 5...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Factor V
Share to Methylenetetrahydrofolate Reductase (NADPH2)

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Plasminogen Activator Inhibitor 1

Share to Prothrombin

Share to Registries

Share to Saudi Arabia

Share to Thrombophilia

Share to Venous Thrombosis

Source

Identifiers

PMID: 19838435

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Saudi Thrombosis and Familial Thrombophilia Registry. Design, rational, and preliminary results.PMID 19838435Read ↗

Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations.Semantic proximity Read ↗

Management of inherited thrombophilia: guide for genetics professionals.Semantic proximity Read ↗

Clinical characteristics and thrombophilia associated gene variants in Egyptians with unprovoked venous thromboembolism: three centers experience.Semantic proximity Read ↗

Inherited Thrombophilia: Implications for Prevention and Treatment of Venous ThromboembolismSemantic proximity Read ↗

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.Semantic proximity Read ↗

Testing for inherited thrombophilia and consequences for antithrombotic prophylaxis in patients with venous thromboembolism and their relativesSemantic proximity Read ↗

Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.Semantic proximity Read ↗

Thrombophilia and venous thromboembolism. International consensus statement. Guidelines according to scientific evidence.Semantic proximity Read ↗

[Frequently associated genotypes to thrombophilia].Semantic proximity Read ↗

Molecular diagnostics of inherited thrombosis.Semantic proximity Read ↗

Genetic Risk Factors of Venous Thromboembolism in the East Algerian Population.Semantic proximity Read ↗

Prevalence of genetic prothrombotic risk factors: 1691G > A FV, 20210G > A PT and 677C > T MTHFR mutations in the Bosnian population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.