Macro- and microvascular endothelial dysfunction modulation by VCAM1 haplotypes of pediatric sickle cell anemia patients

Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity for the HBB:c.20A>T mutation. Children with SCA usually present a systemic vascular disease with profound effects in organs like the brain, with stroke being the most severe end of the cerebral vasc...

Full description

Bibliographic Details
Main Author: Silva, Marisa (author)
Other Authors: Vargas, Sofia (author), Coelho, Andreia (author), Faustino, Paula (author)
Format: conferenceObject
Language:eng
Published: 2021
Subjects:
Sickle Cell Disease
VCAM1
Doenças Genéticas
Hemoglobinopatias
Drepanocitose
Vasculopatia Cerebral
Modificadores Genéticos
Anemia
Online Access:http://hdl.handle.net/10400.18/7447
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/7447

Internet

http://hdl.handle.net/10400.18/7447

Similar Items