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M A Vilaseca

Showing results (51-60 of 118) with videos related to

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Anales Espanoles De Pediatria|May 1, 1991
[Ornithine transcarbamylase deficiency. Biochemical studies in the diagnosis of 4 cases and the identification of carriers]P Briones Godino, M A Vilaseca Busca, L Alvarez Dominguez, 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.
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.
The International Journal of Eating Disorders|January 30, 1999
Antioxidant status in anorexia nervosaD Moyano, C Sierra, N Brandi, 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.
Journal of Inherited Metabolic Disease|August 1, 1998
Feasibility of molecular prenatal diagnosis of glutaric aciduria type I in chorionic villiC Busquets, M J Coll, E Christensen, et al.
Neurology|April 12, 2006
Global and regional volume changes in the brains of patients with phenylketonuriaB Pérez-Dueñas, J Pujol, C Soriano-Mas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 25, 1997
Tocopherol in inborn errors of intermediary metabolismD Moyano, M A Vilaseca, M Pineda, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Anales Espanoles De Pediatria|May 1, 1991
[Ornithine transcarbamylase deficiency. Biochemical studies in the diagnosis of 4 cases and the identification of carriers]P Briones Godino, M A Vilaseca Busca, L Alvarez Dominguez, 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.
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.
The International Journal of Eating Disorders|January 30, 1999
Antioxidant status in anorexia nervosaD Moyano, C Sierra, N Brandi, 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.
Journal of Inherited Metabolic Disease|August 1, 1998
Feasibility of molecular prenatal diagnosis of glutaric aciduria type I in chorionic villiC Busquets, M J Coll, E Christensen, et al.
Neurology|April 12, 2006
Global and regional volume changes in the brains of patients with phenylketonuriaB Pérez-Dueñas, J Pujol, C Soriano-Mas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 25, 1997
Tocopherol in inborn errors of intermediary metabolismD Moyano, M A Vilaseca, M Pineda, et al.
Pageof 12