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Journal of Inherited Metabolic Disease|January 1, 1982
Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiencyJ A DelValle, B Merinero, A Jiménez, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Late onset type of propionic acidaemia: case report and biochemical studiesB Merinero, J A DelValle, A Jiménez, et al.Prenatal Diagnosis|June 1, 1993
First report of prenatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in a pregnancy at riskC Pérez-Cerdá, B Merinero, A Jiménez, et al.Neurologia (Barcelona, Spain)|May 14, 2005
[Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age]I Pascual-Castroviejo, S I Pascual-Pascual, B Merinero, et al.Neurologia (Barcelona, Spain)|August 1, 1994
[Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria]A Martínez Bermejo, I Pascual Castroviejo, B Merinero, et al.JIMD Reports|May 21, 2013
Severe Neonatal Metabolic Decompensation in Methylmalonic Acidemia Caused by CblD DefectR Parini, F Furlan, A Brambilla, et al.Prenatal Diagnosis|October 30, 1998
Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuriaB Merinero, C Pérez-Cerdá, M J Garcia, et al.Clinical Genetics|May 13, 2014
Methylmalonic aciduria cblB type: characterization of two novel mutations and mitochondrial dysfunction studiesS Brasil, E Richard, A Jorge-Finnigan, et al.Biochimica Et Biophysica Acta|February 16, 2010
Mitochondrial bioenergetics and dynamics interplay in complex I-deficient fibroblastsM Morán, H Rivera, M Sánchez-Aragó, et al.Stem Cell Research|April 17, 2018
Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB typeE Richard, S Brasil, A Briso-Montiano, et al.Pageof 4