Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
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Multiple Acyl-CoA Dehydrogenation Deficiency (Glutaric Aciduria Type II) with a Novel Mutation of Electron Transfer Flavoprotein-Dehydrogenase in a Cat.Cyclic vomiting syndrome masking a fatal metabolic disease.Carnitine-acylcarnitine translocase deficiency: experience with four cases in Spain and review of the literature.Growth in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.Infant with hepatomegaly and hypoglycemia: A setting for fatty acid oxidation defects.Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function.Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast.
P2860
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P2860
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 12 January 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@en
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
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type
label
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@en
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@nl
prefLabel
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@en
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@nl
P2093
P1476
Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
@en
P2093
Allan Meldgaard Lund
Ernst Christensen
Helle Vestergaard
Mette Christensen
P2888
P304
P356
10.1007/S10545-009-9000-2
P577
2010-01-12T00:00:00Z