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-a-possible-mechanism-for-neurodegeneration-in-gl2026-09-24T03:57:30.945Zhttps://searchpubmed.org/record/pubmed%3A9266364/d-glyceric-aciduria-in-an-afghan-hound2026-09-24T03:57:30.949Zhttps://searchpubmed.org/record/pubmed%3A9266365/valproate-inhibits-the-mitochondrial-pyruvate-driven-oxidative-phosphorylation-in-vitro2026-09-24T03:57:30.953Zhttps://searchpubmed.org/record/pubmed%3A9266363/mevalonate-kinase-deficiency-in-a-dizygotic-twin-with-mild-mevalonic-aciduria2026-09-24T03:57:30.955Zhttps://searchpubmed.org/record/pubmed%3A9266366/a-case-of-benign-pyruvate-carboxylase-deficiency-with-normal-development2026-09-24T03:57:30.957Zhttps://searchpubmed.org/record/pubmed%3A9266367/muscle-biochemistry-in-thiamin-responsive-anaemia2026-09-24T03:57:30.959Zhttps://searchpubmed.org/record/pubmed%3A9266368/hypoketonuric-3-hydroxydicarboxylic-aciduria-in-five-patients-with-glycogen-storage-disease2026-09-24T03:57:30.962Zhttps://searchpubmed.org/record/pubmed%3A9266369/diagnosis-of-inborn-errors-of-metabolism-by-acylcarnitine-profiling-in-blood-using-tandem-mass-spect2026-09-24T03:57:30.964Zhttps://searchpubmed.org/record/pubmed%3A9266370/improved-detection-of-long-chain-fatty-acid-oxidation-defects-in-intact-cells-using-9-10-3h-oleic-ac2026-09-24T03:57:30.969Zhttps://searchpubmed.org/record/pubmed%3A9266371/molecular-basis-of-long-chain-3-hydroxyacyl-coa-dehydrogenase-deficiency-identification-of-two-new-m2026-09-24T03:57:30.971Zhttps://searchpubmed.org/record/pubmed%3A9266373/short-chain-acyl-coa-dehydrogenase-deficiency-in-a-16-year-old-girl-with-severe-muscle-wasting-and-s2026-09-24T03:57:30.972Zhttps://searchpubmed.org/record/pubmed%3A9266372/broad-specificity-of-carnitine-palmitoyltransferase-ii-towards-long-chain-acyl-coa-beta-oxidation-in2026-09-24T03:57:30.975Zhttps://searchpubmed.org/record/pubmed%3A9266374/smith-lemli-opitz-syndrome-deficient-delta-7-reductase-activity-in-cultured-skin-fibroblasts-and-cho2026-09-24T03:57:30.979Zhttps://searchpubmed.org/record/pubmed%3A9266376/formation-of-2-3-pristenic-acid-and-3-hydroxypristanic-acid-from-pristanic-acid-in-human-liver2026-09-24T03:57:30.982Zhttps://searchpubmed.org/record/pubmed%3A9266375/genetic-heterogeneity-in-patients-with-a-disorder-of-peroxisomal-beta-oxidation-a-complementation-st2026-09-24T03:57:30.985Zhttps://searchpubmed.org/record/pubmed%3A9266377/phytanoyl-coa-hydroxylase-is-not-only-deficient-in-classical-refsum-disease-but-also-in-rhizomelic-c2026-09-24T03:57:30.987Zhttps://searchpubmed.org/record/pubmed%3A9266379/gc-ms-determination-of-guanidinoacetate-in-urine-and-plasma2026-09-24T03:57:30.989Zhttps://searchpubmed.org/record/pubmed%3A9266378/phosphomannomutase-deficiency-is-the-main-cause-of-carbohydrate-deficient-glycoprotein-syndrome-with2026-09-24T03:57:30.990Zhttps://searchpubmed.org/record/pubmed%3A9266380/molecular-analysis-in-23-hunter-disease-families2026-09-24T03:57:30.996Zhttps://searchpubmed.org/record/pubmed%3A9266382/continuous-venovenous-haemodiafiltration-in-the-acute-phase-of-neonatal-maple-syrup-urine-disease2026-09-24T03:57:30.999Zhttps://searchpubmed.org/record/pubmed%3A9266385/adult-psychosocial-outcome-in-early-treated-phenylketonuria2026-09-24T03:57:31.004Zhttps://searchpubmed.org/record/pubmed%3A9266383/abnormal-glutathione-conjugation-in-patients-with-tyrosinaemia-type-i2026-09-24T03:57:31.007Zhttps://searchpubmed.org/record/pubmed%3A9266384/treatment-products-and-approaches-for-phenylketonuria-improved-palatability-and-flexibility-demonstr2026-09-24T03:57:31.013Zhttps://searchpubmed.org/record/pubmed%3A9266381/polyunsaturated-fatty-acids-reverse-the-lysosomal-storage-and-accumulation-of-subunit-9-of-mitochond2026-09-24T03:57:31.016Zhttps://searchpubmed.org/record/pubmed%3A9266386/mitochondrial-abnormalities-of-liver-in-two-children-with-citrullinaemia2026-09-24T03:57:31.018Zhttps://searchpubmed.org/record/pubmed%3A9266388/identification-of-private-mutations-in-patients-with-ornithine-transcarbamylase-deficiency2026-09-24T03:57:31.021Zhttps://searchpubmed.org/record/pubmed%3A9266387/mutation-of-ornithine-transcarbamylase-h136r-in-a-girl-with-severe-intermittent-orotic-aciduria-but2026-09-24T03:57:31.025Zhttps://searchpubmed.org/record/pubmed%3A9266389/clinical-heterogeneity-and-prognosis-in-combined-methylmalonic-aciduria-and-homocystinuria-cblc2026-09-24T03:57:31.033Zhttps://searchpubmed.org/record/pubmed%3A9266391/a-longitudinal-study-of-cognitive-functioning-in-patients-with-classical-galactosaemia-including-a-c2026-09-24T03:57:31.037Zhttps://searchpubmed.org/record/pubmed%3A9266392/a-novel-acid-alpha-glucosidase-mutation-identified-in-a-pakistani-family-with-glycogen-storage-disea2026-09-24T03:57:31.042Zhttps://searchpubmed.org/record/pubmed%3A9266390/biochemical-and-molecular-analysis-of-an-x-linked-case-of-leigh-syndrome-associated-with-thiamin-res2026-09-24T03:57:31.047Zhttps://searchpubmed.org/record/pubmed%3A9266395/highly-increased-csf-concentrations-of-cholesterol-precursors-in-smith-lemli-opitz-syndrome2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