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Abstract
Cancer therapies frequently result in a spectrum of neurocognitive deficits that include impaired learning, memory, attention and speed of information processing. Damage to dynamic neural progenitor cell populations in the brain are emerging as important etiologic factors. Radiation and chemotherapy-induced damage to neural progenitor populations responsible for adult hippocampal neurogenesis and for maintenance of subcortical white matter integrity are now believed to play major roles in the neurocognitive impairment many cancer survivors experience.
View details for DOI 10.1016/j.bbr.2011.05.012
View details for Web of Science ID 000301404000010
View details for PubMedID 21621557
View details for PubMedCentralID PMC3221863