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M A Vilaseca

Showing results (21-30 of 118) with videos related to

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Clinical Chemistry|November 4, 1998
Serum ubiquinone-10 in a pediatric populationR Artuch, J Moreno, M Quintana, et al.
Revista De Neurologia|August 31, 2006
[Diagnosis and treatment of brain creatine deficiency syndromes]A Arias-Dimas, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Biochemical follow-up in late-treated nephropathic cystinosisM A Vilaseca, J A Camacho, P Briones, 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.
Journal of Inherited Metabolic Disease|January 1, 1993
the allopurinol test in patients with Rett syndromeM Pineda, M A Vilaseca, A Vernet, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductaseM A Vilaseca, P Briones, A Ribes, et al.
Developmental Medicine and Child Neurology|January 9, 1999
Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activityM Pineda, A Ribes, C Busquets, 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.
Pageof 12

Showing results (21-30 of 118) with videos related to

Sort By:
Pageof 12
Clinical Chemistry|November 4, 1998
Serum ubiquinone-10 in a pediatric populationR Artuch, J Moreno, M Quintana, et al.
Revista De Neurologia|August 31, 2006
[Diagnosis and treatment of brain creatine deficiency syndromes]A Arias-Dimas, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Biochemical follow-up in late-treated nephropathic cystinosisM A Vilaseca, J A Camacho, P Briones, 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.
Journal of Inherited Metabolic Disease|January 1, 1993
the allopurinol test in patients with Rett syndromeM Pineda, M A Vilaseca, A Vernet, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductaseM A Vilaseca, P Briones, A Ribes, et al.
Developmental Medicine and Child Neurology|January 9, 1999
Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activityM Pineda, A Ribes, C Busquets, 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.
Pageof 12