C. Boix

[Neuropsychological profile of internationally adopted children in Catalonia].

A. López-Sala, V. Fumadó, R. Colomé, 2012, Anales de pediatria.

Hand tremor and orofacial dyskinesia: Clinical manifestations of glutaric aciduria type I in a young girl

A. Ribes, Á. García-Cazorla, E. Fernández-Álvarez, 2003 .

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

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

Cognitive functions in classic phenylketonuria and mild hyperphenylalaninaemia: experience in a paediatric population.

R. Artuch, M. Vilaseca, J. Campistol, 2005, Developmental medicine and child neurology.

Cognitive functions in classic phenylketonuria and mild hyperphenyl‐alaninaemia: experience in a paediatric population

R. Artuch, M. Vilaseca, J. Campistol, 2005 .

Infectious Acute Hemicerebellitis

J. Campistol, A. Sans, C. Boix, 2004, Journal of child neurology.

Cognitive functions in patients with phenylketonuria in long-term treatment with tetrahydrobiopterin.

M. Vilaseca, J. Campistol, N. Lambruschini, 2010, Molecular genetics and metabolism.