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pro vyhledávání: '"Rawan Aldrees"'
Autor:
Ali Alsaad, Abdullah Alghanim, Mohammed Aldawood, Ali Al Zaid, Hussain Aldehneen, Rawan Aldrees, Ammar Alsalem, Sami Albattat, Abbas Al Mutair
Publikováno v:
Heliyon, Vol 10, Iss 14, Pp e34283- (2024)
Sickle cell disease (SCD) is a hereditary blood condition characterized by abnormal hemoglobin, leading to chronic hemolysis and vaso-occlusive complications. Caregivers of children with SCD often experience significant distress, akin to post-traumat
Externí odkaz:
https://doaj.org/article/614b4f8f3725420b90d1f0d177c48376
