Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors

Background: Although 80% of childhood acute lymphoblastic leukemia (ALL) cases are cured with current treatment protocols, exposure to chemotherapeutics or radiation therapy during a vulnerable period of child development has been associated with a high frequency of late adverse effects (LAE). Previ...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Pharmgenomics Pers Med
Main Authors: Nadeau, Geneviève, Ouimet-Grennan, Erika, Aaron, Michelle, Drouin, Simon, Bertout, Laurence, Shalmiev, Albert, Beaulieu, Patrick, St-Onge, Pascal, Veilleux, Louis-Nicolas, Rauch, Frank, Petrykey, Kateryna, Laverdière, Caroline, Sinnett, Daniel, Alos, Nathalie, Krajinovic, Maja
Format: Artigo
Jezik:Inglês
Izdano: Dove 2019
Teme:
Original Research
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6489684/
https://ncbi.nlm.nih.gov/pubmed/31114288
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PGPM.S192924
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