Repositório Científico do Centro Hospitalar do Porto: SNF - Serviço de Neurofisiologia

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Corino de Andrade disease: mechanisms and impact on reproduction

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

Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy

Peripheral Blood Cell Gene Expression Diagnostic for Identifying Symptomatic Transthyretin Amyloidosis Patients: Male and Female Specific Signatures

Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis

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