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The American Journal of Clinical Nutrition|October 28, 1999
Decreased serum ubiquinone-10 concentrations in phenylketonuriaR Artuch, M A Vilaseca, J Moreno, et al.European Journal of Clinical Nutrition|July 25, 2003
Plasma thiols and their determinants in phenylketonuriaC Colomé, R Artuch, C Sierra, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Platelet serotonin concentrations in PKU patients under dietary control and tetrahydrobiopterin treatmentA Ormazabal, M A Vilaseca, B Pérez-Dueñas, et al.Journal of Inherited Metabolic Disease|August 7, 2001
Plasma phenylalanine is associated with decreased serum ubiquinone-10 concentrations in phenylketonuriaR Artuch, C Colomé, M A Vilaseca, et al.Acta Paediatrica (Oslo, Norway : 1992)|September 12, 2002
New approach to osteopenia in phenylketonuric patientsB Pérez-Dueñas, F J Cambra, M A Vilaseca, et al.Human Mutation|April 13, 1999
Two novel mutations in exon 11 of the PAH gene (V1163del TG and P362T) associated with classic phenylketonuira and mild phenylketonuria. Mutations in brief no. 143. OnlineJ Mallolas, J Campistol, N Lambruschini, et al.Human Genetics|December 22, 1999
Mutational spectrum of phenylalanine hydroxylase deficiency in the population resident in Catalonia: genotype-phenotype correlationJ Mallolas, M A Vilaseca, J Campistol, et al.Revista De Neurologia|March 14, 2001
[Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene]J Mallolas, M A Vilaseca, J Campistol, et al.Anales Espanoles De Pediatria|March 23, 2001
[Evolution of a case of tyrosinemia type I treated with NTBC]J Ros Viladoms, M A Vilaseca Buscà, N Lambruschini Ferri, et al.Nutricion Hospitalaria|March 6, 2010
Quality of dietary control in phenylketonuric patients and its relationship with general intelligenceM A Vilaseca, N Lambruschini, Lilianne Gómez-López, et al.Pageof 3