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List of works by Mariana Alves

CLN2/TPP1 deficiency: the novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype.

scientific article published on 23 October 2007

Fluorescent Light-up Probe for the Detection of Protein Aggregates

scientific article published on 11 January 2019

Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: identification of the first large deletion in ASAH1 gene

scientific article published on 4 May 2013

Role for Sit4p-dependent mitochondrial dysfunction in mediating the shortened chronological lifespan and oxidative stress sensitivity of Isc1p-deficient cells.

scientific article published on 28 June 2011

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