Literature DB >> 19408195

Glycoprotein analysis for the diagnostic evaluation of platelet disorders.

Jonathan L Miller1.   

Abstract

Platelet glycoproteins subserve a wide variety of critical functions in blood platelets. Congenital deficiencies or functional abnormalities in platelet glycoproteins may produce serious bleeding disorders such as Glanzmann thrombasthenia or Bernard-Soulier syndrome. Other hematologic disorders, such as Fanconi anemia and various myelodysplastic syndromes, may also be associated with abnormalities in platelet glycoproteins. Additionally, several acquired disorders involving the major platelet glycoproteins are increasingly being recognized. The large number of techniques, now available to characterize platelet glycoprotein disorders, reflect the many advances in biochemistry, molecular analysis, flow cytometry, and, most recently, proteomics. The application of platelet glycoprotein analysis to a wide range of clinical disorders is reviewed in this article.

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Year:  2009        PMID: 19408195     DOI: 10.1055/s-0029-1220330

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


  3 in total

1.  Evaluation of platelet surface glycoproteins in patients with Glanzmann thrombasthenia: Association with bleeding symptoms.

Authors:  Deepti Mutreja; Rahul Kumar Sharma; Abhishek Purohit; Mukul Aggarwal; Renu Saxena
Journal:  Indian J Med Res       Date:  2017-05       Impact factor: 2.375

Review 2.  Glanzmann thrombasthenia: genetic basis and clinical correlates.

Authors:  Juliana Perez Botero; Kristy Lee; Brian R Branchford; Paul F Bray; Kathleen Freson; Michele P Lambert; Minjie Luo; Shruthi Mohan; Justyne E Ross; Wolfgang Bergmeier; Jorge Di Paola
Journal:  Haematologica       Date:  2020-03-05       Impact factor: 9.941

3.  Blood management strategies in congenital Glanzmann thrombasthenia at a hematology referral center.

Authors:  Ganesh Kasinathan; Jameela Sathar
Journal:  Blood Res       Date:  2021-12-31
  3 in total

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