Ethical Issues
Multiple Allele Traits
iPS Cell Differentiation
Ethical Dilemmas I
Pedigree Analysis
Sputum Studies II: Culture and Sensitivity
You might also read
Articles linked to this work by shared authors, journal, and citation graph.
Updated: Jun 20, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Siddika S Mulchan1,2, Christopher B Theriault3, Susan DiVietro3,4,5
1Connecticut Children's, University of Connecticut School of Medicine, Farmington, USA. ssmulchan@gmail.com.
Pediatric providers show implicit racial bias, but virtual patient scenarios did not reveal differences in pain care decisions for Black versus White youth with sickle cell disease (SCD). Standardized protocols may mitigate bias in clinical practice.
05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
08:23Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
Area of Science:
Background:
Purpose of the Study:
Main Methods:
Main Results:
Conclusions: