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

Legg-perthes disease and heritable thrombophilia.

Journal of pediatric orthopedics - 1 Jan 2000

López-Franco Mariano, González-Morán Gaspar, De Lucas José Carlos, Llamas Pilar, de Velasco Jaime Fernández, Vivancos José Carlos, Epeldegui-Torre Tomás

Abstract excerpt

The etiology of Perthes' disease is unclear. Recent reports have suggested that inheritable thrombophilic disorders may be one of its pathogenetic causes. The G20210A prothrombin gene, factor V Leiden, and MTHFR C677T mutations have been identified as predisposing genetic factors for thrombosis....

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to Electrophoresis, Agar Gel
Share to Factor V

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Odds Ratio

Share to Polymerase Chain Reaction

Share to Prothrombin

Share to Thrombophilia

Source

Identifiers

PMID: 15958894
DOI: 10.1097/01.bpo.0000158781.29979.cf

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15958894-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Legg-perthes disease and heritable thrombophilia.PMID 15958894Read ↗

Perthes' disease and the search for genetic associations: collagen mutations, Gaucher's disease and thrombophilia.Semantic proximity Read ↗

[Incidence of thrombophilic factor V Leiden and prothrombin G20210A mutation in Perthes disease--a pilot study].Semantic proximity Read ↗

Meta‐analysis of hypercoagulability genetic polymorphisms in perthes diseaseSemantic proximity Read ↗

Prospective reevaluation of the association between thrombotic diathesis and legg-perthes disease.Semantic proximity Read ↗

Hemostatic markers and polymorphisms in three families with Legg-Calvé-Perthes diseaseSemantic proximity Read ↗

Familial Cases of Legg-Calvé-Perthes Disease-Hemostatic and Molecular Markers.Semantic proximity Read ↗

Resistance to activated protein C and Legg-Perthes disease.Semantic proximity Read ↗

The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease.Semantic proximity Read ↗

Familial cases of Mexican patients with Legg-Calvé-Perthes diseaseSemantic proximity Read ↗

Hemostatic markers and polymorphisms in three Mexican families with Legg-Calvé-Perthes disease.Semantic proximity Read ↗

Association of MTHFR rs1801133 and Homocysteine With Legg-Calvé-Perthes Disease in Mexican PatientsSemantic proximity Read ↗

Association of MTHFR rs1801133 and homocysteine with Legg-Calvé-Perthes disease in Mexican patients.Semantic proximity Read ↗

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