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Diagnóstico y seguimiento de 23 niños con acidurias orgánicas
(Sociedad Médica de Santiago, 2002)
Acidúrias D-2-hidroxiglutárica e L-2-hidroxiglutárica: uma revisão da literatura
(HCPA/FAMED/UFRGS, 2016)
Aciduria glutárica tipo II a propósito de un caso
(Sociedad Venezolana de Puericultura y Pediatría, 2022)
Aciduria D-2-hidroxiglutárica. Reporte de dos casos.
(Universidad del Zulia, 2013)
Evidence in Colombia of 625G>A polymorphism in the short chain acyl-CoA dehydrogenase gene, a variation which could cause glutaric aciduria in our populations.
(2011-11-16)
Introduction: Short-chain acyl-CoA dehydrogenase (SCAD) is a homotetrameric mitochondrial flavoenzyme that
catalyzes the initial reaction in short-chain fatty acid b-oxidation. The SCAD gene is located on chromosome 12q22 ...
Dificuldades no diagnostico e manejo da acidemia metilmalônica - relato de caso sugestivoDifficulties in diagnosis and treatment of methylmalonic aciduria - suggestive case report
(Sociedade de Pediatria do Estado do Rio de Janeiro, 2015)