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Autor:
Mansour Alkobtawi, Maria Sbeih, Karim Souaid, Qui Trung Ngô, Dany Nassar, Hugo Arbes, Henri Guillet, Anoosha Habibi, Pablo Bartolucci, Mathieu Castela, Sélim Aractingi, Bénédicte Oulès
Publikováno v:
Haematologica, Vol 108, Iss 7 (2022)
Leg ulcers are a major complication of sickle cell disease (SCD). They are particularly challenging to treat and innovative therapies are needed. We previously showed that the healing of SCD ulcers is delayed because of decreased angiogenesis. During
Externí odkaz:
https://doaj.org/article/5b752d2f45954d36a6e2002e4d35d484