(FM) Pediatría
Departamento académico
Radboud University Nijmegen Medical Centre
Nimega, HolandaPublicacions en col·laboració amb investigadors/es de Radboud University Nijmegen Medical Centre (5)
2023
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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
The Lancet. Oncology, Vol. 24, Núm. 1, pp. 91-106
2022
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SLC7A8 coding for LAT2 is associated with early disease progression in osteosarcoma and transports doxorubicin
Frontiers in Pharmacology, Vol. 13
2020
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Sarcoma treatment in the era of molecular medicine
EMBO Molecular Medicine, Vol. 12, Núm. 11
2014
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Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: Two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts
PLoS ONE, Vol. 9, Núm. 12
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The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: A meta-analysis in patients with cancer
Pharmacogenomics Journal, Vol. 14, Núm. 2, pp. 115-119