Genetic modulation of stroke in children with sickle cell anaemia

Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of haemoglobin S (HbS). The pathophysiology of the disease is centred on HbS polymerization inside the red blood cells, which become sickle-shaped (SSRBCs), rigid, viscous and adherent-prone to the vascul...

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Detalhes bibliográficos
Autor principal: Silva, Marisa (author)
Outros Autores: Vargas, Sofia (author), Coelho, Andreia (author), Mendonça, Joana (author), Vieira, Luís (author), Kjollerstrom, Paula (author), Maia, Raquel (author), Silva, Rita (author), Dias, Alexandra (author), Ferreira, Teresa (author), Morais, Anabela (author), Mota Soares, Isabel (author), Lavinha, João (author), Faustino, Paula (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2020
Assuntos:
Sickle Cell Anaemia
Drepanocitose
Anemia das Células Falciformes
Hemoglobinopatias
AVC
Modificadores Genéticos
Vasculopatia cerebral
Medicina Personalizada
Doenças Genéticas
Doenças Raras
Genética Humana
Texto completo:http://hdl.handle.net/10400.18/6811
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/6811

Texto Completo

http://hdl.handle.net/10400.18/6811

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