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Recent Advances in Sickle-Cell Disease Therapies: A Review of Voxelotor, Crizanlizumab, and L-glutamine

Sickle-cell disease (SCD) is an inherited hemoglobinopathy, causing lifelong complications such as painful vaso-occlusive episodes, acute chest syndrome, stroke, chronic anemia, and end-organ damage, with negative effects on quality of life and life expectancy. Within the last five years, three new...

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Detalles Bibliográficos
Autores principales:	Migotsky, Michael, Beestrum, Molly, Badawy, Sherif M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610018/ https://www.ncbi.nlm.nih.gov/pubmed/36287444 http://dx.doi.org/10.3390/pharmacy10050123

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