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M A Vilaseca

Showing results (11-20 of 118) with videos related to

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Prenatal Diagnosis|June 1, 1992
A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)M I Tejada, A Uribarren, P Briones, et al.
Revista De Neurologia|April 1, 2000
[Risk factors in cerebrovascular disease in childhood]E Cardo, M Pineda, M A Vilaseca, et al.
Revista De Neurologia|October 21, 1999
[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone]R Artuch, C Colomé, M A Vilaseca, et al.
Revista De Neurologia|January 1, 1996
[Primary leptomeningeal melanomatosis in a 6-year-old child]G Monsó, A Vernet, V Cusí, et al.
European Journal of Clinical Nutrition|April 16, 1998
Plasma total-homocysteine in anorexia nervosaD Moyano, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Increased urine methylmalonic acid excretion in infants with apnoeasR Artuch, M Calvo, A Ribes, et al.
Neuropediatrics|January 24, 2006
Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: treatment with folinic acidA Ormazabal, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyA Ribes, P Briones, M A Vilaseca, et al.
Medicina Clinica|October 2, 1993
[Diagnosis of ornithine carbamoyl transferase deficiency and heterozygote detection with allopurinol loading test]M Pineda, M A Vilaseca, A Mas, et al.
Revista De Neurologia|December 2, 2004
[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system]A Ormazábal, R Artuch, M A Vilaseca, et al.
Pageof 12

Showing results (11-20 of 118) with videos related to

Sort By:
Pageof 12
Prenatal Diagnosis|June 1, 1992
A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)M I Tejada, A Uribarren, P Briones, et al.
Revista De Neurologia|April 1, 2000
[Risk factors in cerebrovascular disease in childhood]E Cardo, M Pineda, M A Vilaseca, et al.
Revista De Neurologia|October 21, 1999
[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone]R Artuch, C Colomé, M A Vilaseca, et al.
Revista De Neurologia|January 1, 1996
[Primary leptomeningeal melanomatosis in a 6-year-old child]G Monsó, A Vernet, V Cusí, et al.
European Journal of Clinical Nutrition|April 16, 1998
Plasma total-homocysteine in anorexia nervosaD Moyano, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Increased urine methylmalonic acid excretion in infants with apnoeasR Artuch, M Calvo, A Ribes, et al.
Neuropediatrics|January 24, 2006
Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: treatment with folinic acidA Ormazabal, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyA Ribes, P Briones, M A Vilaseca, et al.
Medicina Clinica|October 2, 1993
[Diagnosis of ornithine carbamoyl transferase deficiency and heterozygote detection with allopurinol loading test]M Pineda, M A Vilaseca, A Mas, et al.
Revista De Neurologia|December 2, 2004
[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system]A Ormazábal, R Artuch, M A Vilaseca, et al.
Pageof 12