Pediatría
Departamento
Oslo University Hospital
Oslo, NoruegaPublicaciones en colaboración con investigadoras/es de Oslo University Hospital (8)
2024
2022
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Identification and Functional Analysis of a Novel CTNNB1 Mutation in Pediatric Medulloblastoma
Cancers, Vol. 14, Núm. 2
2021
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Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Nature Communications, Vol. 12, Núm. 1
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MMADHC premature termination codons in the pathogenesis of cobalamin D disorder: Potential of translational readthrough reconstitution
Molecular Genetics and Metabolism Reports, Vol. 26
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Protein Tyrosine Phosphatases in Neuroblastoma: Emerging Roles as Biomarkers and Therapeutic Targets
Frontiers in Cell and Developmental Biology, Vol. 9
2020
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Brain circuit alterations and cognitive disability in late-onset cobalamin d disorder
Journal of Clinical Medicine, Vol. 9, Núm. 4
2017
2007
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Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: A meta-analysis
Tissue Antigens, Vol. 70, Núm. 2, pp. 110-127