I. Catalina

Neurological complications of COVID‐19 in hospitalized patients: The registry of a neurology department in the first wave of the pandemic

F. Grandas, A. Massot-Tarrús, F. Díaz-Otero, 2021, European journal of neurology.

Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study

M. Desco, Y. Alemán-Gómez, F. Grandas, 2022, Journal of Neurology.

Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4

M. Desco, F. Grandas, Susanna Carmona, 2021, Journal of Neurology.

Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4)

M. Desco, A. Lage-Castellanos, F. Grandas, 2021, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

J. Clarimón, A. Lleó, P. Pástor, 2013, Human mutation.

Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

V. Álvarez, F. Grandas, J. Infante, 2019, Movement disorders : official journal of the Movement Disorder Society.

Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

V. Álvarez, F. Grandas, J. Infante, 2019, Movement disorders : official journal of the Movement Disorder Society.