M. González

Prevalence of sleep disorders in early-treated phenylketonuric children and adolescents. Correlation with dopamine and serotonin status.

D. Cuadras, A. Ormazabal, R. Artuch, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Impaired Neurotransmission in Early-treated Phenylketonuria Patients.

R. Artuch, J. Campistol, R. Gassió, 2016, Seminars in pediatric neurology.

Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unit.

M. Vilaseca, J. Campistol, R. Gassió, 2011, Molecular genetics and metabolism.

The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype

M. Baumgartner, E. Rodrigues, C. Ortez, 2015, Journal of Inherited Metabolic Disease.

Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders

J. Armstrong, A. Ormazabal, R. Artuch, 2015, Orphanet Journal of Rare Diseases.

Plasma coenzyme Q10 status is impaired in selected genetic conditions

Eduardo Ruiz-Pesini, Julio Montoya, Rafael Artuch, 2019, Scientific Reports.

White matter microstructural damage in early treated phenylketonuric patients

P. Ripollés, A. Ormazabal, R. Artuch, 2018, Orphanet Journal of Rare Diseases.

Effect of carglumic acid with or without ammonia scavengers on hyperammonaemia in acute decompensation episodes of organic acidurias

A. Chakrapani, Á. García-Cazorla, M. Donati, 2018, Orphanet Journal of Rare Diseases.

Plasma coenzyme Q10 status is impaired in selected genetic conditions

P. Navas, E. Ruiz-Pesini, R. Artuch, 2019, Scientific Reports.