scispace - formally typeset
S

Swee Lay Thein

Researcher at National Institutes of Health

Publications -  335
Citations -  21617

Swee Lay Thein is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Fetal hemoglobin & Population. The author has an hindex of 62, co-authored 316 publications receiving 19670 citations. Previous affiliations of Swee Lay Thein include King's College & University of Oxford.

Papers
More filters
Journal ArticleDOI

Airway and alveolar nitric oxide production, lung function, and pulmonary blood flow in sickle cell disease

TL;DR: Airway NO flux was not elevated in the SCD children nor correlated with airways obstruction, suggesting that airway obstruction, at least in someSCD children, is not due to asthma.
Journal ArticleDOI

Optimal disease management and health monitoring in adults with sickle cell disease.

TL;DR: The approach to managing adults with SCD needs to reevaluate by putting a greater emphasis on multidisciplinary care while proactively considering curative options (hematopoietic stem cell transplant and gene therapy) and experimental pharmacological agents for adults withSCD of all ages before complications render the patients ineligible for these treatments.
Journal ArticleDOI

Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK

TL;DR: The incidence of VTE in the patient cohort was higher than in the non-SCD black population; patients of all SCD genotypes with VTE had significantly elevated steady-state platelet counts compared to those without; and consideration of longer VTE prophylaxis for acute hospital admissions in SCD is suggested.
Journal ArticleDOI

NLRP3 inflammasome and bruton tyrosine kinase inhibition interferes with upregulated platelet aggregation and in vitro thrombus formation in sickle cell mice.

TL;DR: Platelet aggregation and in vitro thrombus formation were upregulated in SCD mice and were inhibited when mice were subjected to pharmacological inhibition of NLRP3 and BTK.