M. de Lemus

Design of a Non-Interventional Study to Validate a Set of Patient- and Caregiver-Oriented Measurements to Assess Health Outcomes in Spinal Muscular Atrophy (SMA-TOOL Study)

J. Maurino, M. Madruga-Garrido, J. Vázquez-Costa, 2021, Neurology and Therapy.

Physical fatigue and perceived fatigability in adolescents and adults with spinal muscular atrophy: a pilot study

J. Vázquez-Costa, M. de Lemus, I. P. Castellano, 2022, Neurology Perspectives.

Position Statement: Sharing of Clinical Research Data in Spinal Muscular Atrophy to Accelerate Research and Improve Outcomes for Patients

R. Finkel, F. Muntoni, Hanns Lochmüller, 2018, Journal of neuromuscular diseases.

The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018.

E. Mazzone, Hanns Lochmüller, B. V. van Engelen, 2019, Journal of neuromuscular diseases.

Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study

J. Maurino, R. Rojas-García, J. Vázquez-Costa, 2022, Neurology and Therapy.

Understanding the relationship between the 32-item motor function measure and daily activities from an individual with spinal muscular atrophy and their caregivers’ perspective: a two-part study

C. Vuillerot, R. Arbuckle, T. Duong, 2021, BMC Neurology.