Repositório Científico do Centro Hospitalar do Porto: SNP - Serviço de Neuropatologia

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Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene

Nonprimary Cytomegalovirus Fetal Infection

Hypoxia-mediated upregulation of MCT1 expression supports the glycolytic phenotype of glioblastomas

Post-mortem assessment in vascular dementia: advances and aspirations

Hansen Neuropathy: Still a Possible Diagnosis in the Investigation of a Peripheral Neuropathy

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