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Journal of Inherited Metabolic Disease|January 1, 1992
Investigation of enzyme defects in children with lactic acidosisB Merinero, C Pérez-Cerda, M UgarteJournal of Inherited Metabolic Disease|October 27, 2004
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiencyE Christensen, A Ribes, B Merinero, et al.Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Urinary guanidinoacetate and creatine levels in patients with HPRT deficiencyA Verdú, R J Torres, B Merinero, et al.Revista Espanola De Fisiologia|January 1, 1982
[Human fibroblast bank for studying amino acid disorders and organic acidemias]J A del Valle, B Merinero, C Pérez-Cerdá, et al.Prenatal Diagnosis|December 23, 2004
Prenatal diagnosis of propionic acidemiaC Pérez-Cerdá, B Pérez, B Merinero, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 2014
Enzymatic diagnosis of homocystinuria by determination of cystathionine-ß-synthase activity in plasma using LC-MS/MSP Alcaide, J Krijt, P Ruiz-Sala, et al.Prenatal Diagnosis|July 1, 1989
Non-ketotic hyperglycinaemia: glycine/serine ratio in amniotic fluid--an unreliable method for prenatal diagnosisM J Garcia-Muñoz, J Belloque, B Merinero, et al.Human Mutation|October 29, 2009
Pseudoexon exclusion by antisense therapy in methylmalonic aciduria (MMAuria)B Pérez, A Rincón, A Jorge-Finnigan, et al.Anales Espanoles De Pediatria|April 3, 2002
[Neonatal onset methylmalonic aciduria and homocystinuria:Biochemical and clinical improvement with betaine therapy]A Urbón Artero, J Aldana Gómez, C Reig Del Moral, et al.Prenatal Diagnosis|October 4, 2000
Prenatal molecular diagnosis of glutaric aciduria type I by direct mutation analysisC Busquets, M J Coll, B Merinero, et al.Pageof 4