A. Felipe

Investigations in GABAA receptor antibody-associated encephalitis

M. Rosenfeld, J. Dalmau, F. Graus, 2017, Neurology.

Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment

D. Cuadras, C. Pérez-Cerdá, R. Artuch, 2015, Orphanet Journal of Rare Diseases.

A quantitative assessment of the evolution of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG)

D. Cuadras, B. Pérez-Dueñas, A. Macaya, 2017, Orphanet Journal of Rare Diseases.

Clinical Assessment of Dysarthria in Children with Cerebellar Syndrome Associated with PMM2-CDG

D. Cuadras, R. Artuch, M. Couce, 2018, Neuropediatrics.