Gisela Nogales-Gadea

A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patients

Alejandro Lucia, Ana Cabello, Alberto Blazquez, 2007, Human mutation.

Delivery is key: lessons learnt from developing splice‐switching antisense therapies

Samir El Andaloussi, Bård Smedsrød, B. Smedsrød, 2017, EMBO molecular medicine.

A Transcriptomic Approach to Search for Novel Phenotypic Regulators in McArdle Disease

Alejandro Lucia, Antoni L. Andreu, A. Lucia, 2012, PloS one.

McArdle disease: what do neurologists need to know?

Alejandro Lucia, Margarita Pérez, A. Lucia, 2008, Nature Clinical Practice Neurology.