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Revista De Neurologia|August 31, 2006
[Diagnosis and treatment of brain creatine deficiency syndromes]A Arias-Dimas, M A Vilaseca, R Artuch, et al.Clinical Chemistry and Laboratory Medicine|January 5, 2001
Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylationC Colomé, I Ferrer, R Artuch, et al.Clinical Biochemistry|August 28, 2001
Is there a relationship between plasma phenylalanine and cholesterol in phenylketonuric patients under dietary treatment?C Colomé, R Artuch, N Lambruschini, et al.Neuropediatrics|May 6, 2004
Cerebrospinal fluid concentrations of idebenone in Friedreich ataxia patientsR Artuch, A Aracil, A Mas, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 26, 1999
Evaluation of hyperhomocysteinaemia in children with strokeE Cardo, M A Vilaseca, J Campistol, et al.Diabetes Care|June 17, 2000
Total homocysteine in patients with type 1 diabetesC Pavía, I Ferrer, C Valls, et al.Neuropediatrics|October 9, 2002
Friedreich's ataxia: idebenone treatment in early stage patientsR Artuch, A Aracil, A Mas, et al.The American Journal of Clinical Nutrition|October 28, 1999
Decreased serum ubiquinone-10 concentrations in phenylketonuriaR Artuch, M A Vilaseca, J Moreno, et al.Brain & Development|December 12, 2001
Oxidative stress in Rett syndromeC Sierra, M A Vilaseca, N Brandi, et al.Journal of Child Neurology|June 1, 2000
Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin statusE Cardo, E Monrós, C Colomé, et al.Pageof 8