Ban B. Dawood

Lode Lane
Solihull, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 8 publications

Prescribing patterns of oral antiplatelets in Wales: evolving trends from 2005 to 2016.

Prescribing patterns of oral antiplatelets in Wales: evolving trends from 2005 to 2016.

Journal: Future cardiology

Published: June 26, 2018

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects.

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects.

Journal: Haematologica

Published: March 17, 2016

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

Journal: The Journal of clinical investigation

Published: January 13, 2015

Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders.

Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders.

Journal: Journal of thrombosis and haemostasis : JTH

Published: November 08, 2013

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.

Journal: Blood

Published: October 09, 2013

A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction.

A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction.

Journal: Thrombosis and haemostasis

Published: August 16, 2013

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel.

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel.

Journal: Blood

Published: September 25, 2012

MYBL2 haploinsufficiency increases susceptibility to age-related haematopoietic neoplasia.

MYBL2 haploinsufficiency increases susceptibility to age-related haematopoietic neoplasia.

Journal: Leukemia

Published: August 23, 2012

Showing 1-8 of 8

Last Updated: 09/26/2026