Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studies-Reference-Cited by-同舟云学术

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Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studies

Published:2025-02 Issue: Volume:110 Page:102893
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Gu Sean X.,Butt Ayesha,Schulz Vincent P.,Rinder Henry M.,Lee Alfred I.,Gallagher Patrick G.,Hwa John,Bona Robert D.

Funder

Yale University School of Medicine

National Institutes of Health

Frederick A. DeLuca Foundation

National Heart Lung and Blood Institute Division of Intramural Research

Publisher

Elsevier BV

Reference16 articles.

1. Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey;Gresele;J. Thromb. Haemost.,2014

2. Recommendations for the standardization of light transmission Aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH;Cattaneo;J. Thromb. Haemost.,2013

3. Comparison of multiple electrode aggregometry with lumi-aggregometry for the diagnosis of patients with mild bleeding disorders;Al Ghaithi;J. Thromb. Haemost.,2017

4. Diagnosis and management of inherited thrombocytopenias;Balduini;Semin. Thromb. Hemost.,2013

5. Mass cytometry reveals distinct platelet subtypes in healthy subjects and novel alterations in surface glycoproteins in Glanzmann Thrombasthenia;Blair;Sci. Rep.,2018

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