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11
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.pdf
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening
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7
Long-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies induce oxidative stress in rat brain.pdf
Long-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies induce oxidative stress in rat brainLong-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies induce oxidative stress in rat brainLong-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies induce oxidative stress in rat brain
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7
Disturbance of mitochondrial energy homeostasis caused by the metabolites accumulating in LCHAD and MTP deficiencies in rat brain.pdf
Disturbance of mitochondrial energy homeostasis caused by the metabolites accumulating in LCHAD and MTP deficiencies in rat brain
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9
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.pdf
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening
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6
Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein...pdf
Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency
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3
long-chain l 3-hydroxyacyl-coa dehydrogenase (lchad) deficiency does not appear to be the primary cause of lipid myopathy in patients with bannayan-riley-ruvalcaba syndrome (brrs).pdf
long-chain l 3-hydroxyacyl-coa dehydrogenase (lchad) deficiency does not appear to be the primary cause of lipid myopathy in patients with bannayan-riley-ruvalcaba syndrome (brrs)
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8
Increased lipolysis in LCHAD deficiency.pdf
Increased lipolysis in LCHAD deficiency
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5
infection a ebv revelatrice a l'age de 3 ans d'un deficit en 3-hydroxyacyl-coa deshydrogenase des acides gras a chane longue (lchad).pdf
infection à ebv révélatrice à l’age de 3 ans d’un déficit en 3-hydroxyacyl-coa déshydrogénase des acides gras à chane longue (lchad)
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