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...

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Detalhes bibliográficos
Autor principal: Silva, Marisa (author)
Outros Autores: Vargas, Sofia (author), Coelho, Andreia (author), Faustino, Paula (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2021
Assuntos:
Sickle Cell Disease
VCAM1
Doenças Genéticas
Hemoglobinopatias
Drepanocitose
Vasculopatia Cerebral
Modificadores Genéticos
Anemia
Texto completo:http://hdl.handle.net/10400.18/7447
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/7447

Texto Completo

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

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