Literature DB >> 15706472

A review of the clinical and diagnostic utility of laboratory tests for the detection of congenital thrombophilia.

Armando Tripodi1.   

Abstract

Laboratory tests to detect congenital thrombophilia are frequently requested by clinicians. This review attempts to define (1) whether and to what extent laboratory testing may help clinicians make decisions on patient management, (2) the types of conditions to be investigated, and (3) the types of testing to be performed for each condition.

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Year:  2005        PMID: 15706472     DOI: 10.1055/s-2005-863802

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  2 in total

Review 1.  Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype. A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology.

Authors:  David Bosler; Joan Mattson; Domnita Crisan
Journal:  J Mol Diagn       Date:  2006-09       Impact factor: 5.568

2.  "Am I carrier?" The patient's lived experience of thrombophilia genetic screening and its outcome.

Authors:  Guendalina Graffigna; Daniela Leone; Elena Vegni
Journal:  Health Psychol Behav Med       Date:  2014-06-04
  2 in total

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