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M A Vilaseca

Showing results (71-80 of 118) with videos related to

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European Journal of Clinical Nutrition|September 25, 2003
Low serum carnitine in HIV-infected children on antiretroviral treatmentM A Vilaseca, R Artuch, C Sierra, et al.
Clinical Biochemistry|November 14, 2000
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseasesR Artuch, C Colomé, A Playán, et al.
Revista De Neurologia|March 27, 2007
[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease]J Campistol, A Arias-Dimas, P Poo, et al.
Anales Espanoles De Pediatria|September 25, 1999
[Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]J Campistol Plana, M Arellano Pedrola, P Poo Argüelles, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Requirement of high biotin doses in a case of biotinidase deficiencyE Riudor, M A Vilaseca, P Briones, et al.
Journal of Inherited Metabolic Disease|March 21, 2007
Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitisE Quintana, S Gala, A García-Cazorla, et al.
European Journal of Clinical Investigation|December 12, 2001
Hyperhomocysteinaemia and folate deficiency in human immunodeficiency virus-infected childrenM A Vilaseca, C Sierra, C Colomé, et al.
Brain & Development|July 1, 1995
An atypical French form of pyruvate carboxylase deficiencyM Pineda, J Campistol, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|December 25, 2004
Two successful pregnancies in pyridoxine-nonresponsive homocystinuriaM A Vilaseca, M L Cuartero, M Martinez de Salinas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 1998
Antioxidant status in hyperphenylalaninemiaC Sierra, M A Vilaseca, D Moyano, et al.
Pageof 12

Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
European Journal of Clinical Nutrition|September 25, 2003
Low serum carnitine in HIV-infected children on antiretroviral treatmentM A Vilaseca, R Artuch, C Sierra, et al.
Clinical Biochemistry|November 14, 2000
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseasesR Artuch, C Colomé, A Playán, et al.
Revista De Neurologia|March 27, 2007
[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease]J Campistol, A Arias-Dimas, P Poo, et al.
Anales Espanoles De Pediatria|September 25, 1999
[Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]J Campistol Plana, M Arellano Pedrola, P Poo Argüelles, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Requirement of high biotin doses in a case of biotinidase deficiencyE Riudor, M A Vilaseca, P Briones, et al.
Journal of Inherited Metabolic Disease|March 21, 2007
Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitisE Quintana, S Gala, A García-Cazorla, et al.
European Journal of Clinical Investigation|December 12, 2001
Hyperhomocysteinaemia and folate deficiency in human immunodeficiency virus-infected childrenM A Vilaseca, C Sierra, C Colomé, et al.
Brain & Development|July 1, 1995
An atypical French form of pyruvate carboxylase deficiencyM Pineda, J Campistol, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|December 25, 2004
Two successful pregnancies in pyridoxine-nonresponsive homocystinuriaM A Vilaseca, M L Cuartero, M Martinez de Salinas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 1998
Antioxidant status in hyperphenylalaninemiaC Sierra, M A Vilaseca, D Moyano, et al.
Pageof 12