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Nutricion Hospitalaria|April 27, 2011
Long-chain polyunsaturated fatty acid concentration in patients with inborn errors of metabolismM A Vilaseca, L Gómez-López, N Lambruschini, 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.Molecular Genetics and Metabolism|November 16, 2001
Phenotype and genotype heterogeneity in Mediterranean citrullinemiaM A Vilaseca, K Kobayashi, P Briones, et al.Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001
Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genesJ Mallolas, M A Vilaseca, C Pavia, et al.Journal of Clinical Gastroenterology|December 1, 1993
Treatment of chronic hepatitis B in children with recombinant alfa interferon. Different response according to age at infectionM Bruguera, L Amat, O Garcia, et al.Clinical Biochemistry|April 19, 2011
Assessment of plasma ammonia and glutamine concentrations in urea cycle disordersM Serrano, A Ormazábal, M A Vilaseca, et al.Anales De Pediatria (Barcelona, Spain : 2003)|November 4, 2011
[Epidemiological study of the metabolic diseases with homocystinuria in Spain]M C García-Jiménez, A Baldellou, M T García-Silva, et al.Pageof 3