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A Vilaseca

Showing results (41-50 of 133) with videos related to

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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.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|July 18, 2009
Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylationEster Quintana, Raquel Montero, Mercedes Casado, et al.
Molecular Genetics and Metabolism|August 9, 2011
Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unitMaría J González, Alfonso P Gutiérrez, Rosa Gassió, et al.
Rehabilitacion|September 7, 2021
[Efficacy of collagen infiltrations in the pelvic pain caused by episiotomy and caesarean scars. Pilot randomized clinical trial]G Romero-Cullerés, A Amela-Arévalo, C Jané-Feixas, et al.
Developmental Medicine and Child Neurology|March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuriaE Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria|September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
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.
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.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
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.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|July 18, 2009
Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylationEster Quintana, Raquel Montero, Mercedes Casado, et al.
Molecular Genetics and Metabolism|August 9, 2011
Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unitMaría J González, Alfonso P Gutiérrez, Rosa Gassió, et al.
Rehabilitacion|September 7, 2021
[Efficacy of collagen infiltrations in the pelvic pain caused by episiotomy and caesarean scars. Pilot randomized clinical trial]G Romero-Cullerés, A Amela-Arévalo, C Jané-Feixas, et al.
Developmental Medicine and Child Neurology|March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuriaE Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria|September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
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.
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.
Pageof 14