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Revista De Neurologia|September 20, 2001
[Bilateral hypodensity of the basal ganglia. Clinico-evolutionary correlation in children]A Martínez Bermejo, J Arcas, M C Roche, et al.Data in Brief|April 8, 2016
Dataset reporting BCKDK interference in a BCAA-catabolism restricted environmentI Bravo-Alonso, A Oyarzabal, M Sánchez-Aragó, et al.Journal of Inherited Metabolic Disease|March 26, 2009
Creatine transporter deficiency in two adult patients with static encephalopathyA Sempere, C Fons, A Arias, et al.Biochimica Et Biophysica Acta|January 26, 2016
Mitochondrial response to the BCKDK-deficiency: Some clues to understand the positive dietary response in this form of autismA Oyarzabal, I Bravo-Alonso, M Sánchez-Aragó, et al.Journal of Inherited Metabolic Disease|January 1, 1984
A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndromeJ A Del Valle, M J Garcia, B Merinero, et al.Neuropediatrics|October 1, 1995
Variable clinical and biochemical presentation of seven Spanish cases with glutaryl-CoA-dehydrogenase deficiencyB Merinero, C Pérez-Cerdá, L M Font, et al.Anales Espanoles De Pediatria|July 1, 1988
[Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency]B Merinero Cortés, J del Valle Martínez, C Pérez-Cerdá Silvestre, et al.Nucleosides, Nucleotides & Nucleic Acids|June 19, 2014
Thirteen years experience with selective screening for disorders in purine and pyrimidine metabolismM Castro, R Carrillo, F García, et al.Journal of Inherited Metabolic Disease|October 13, 1999
Adolescent myopathic presentation in two sisters with very long-chain acyl-CoA dehydrogenase deficiencyB Merinero, S I Pascual Pascual, C Pérez-Cerdá, et al.Anales Espanoles De Pediatria|November 1, 1983
[3 patients with maple syrup urine disease]B Merinero, J A del Valle, M J García, et al.Pageof 4