Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. - Wikidata - awgldk - TriplyDB

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

http://www.wikidata.org/entity/Q33617698

about

Carnitine supplementation for inborn errors of metabolism Carnitine supplementation for inborn errors of metabolism Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies EFFECT OF FEEDING, EXERCISE AND GENOTYPE ON PLASMA 3-HYDROXYACYLCARNITINES IN CHILDREN WITH LCHAD DEFICIENCY Mitochondrial Trifunctional Protein Defects: Clinical Implications and Therapeutic Approaches Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorder.Diagnosis, Treatment, and Clinical Outcome of Patients with Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency.Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencies.Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).Characterization of Chorioretinopathy Associated with Mitochondrial Trifunctional Protein Disorders: Long-Term Follow-up of 21 Cases.Growth in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.Acylcarnitines--old actors auditioning for new roles in metabolic physiology.Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.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.Identification of a novel single nucleotide polymorphism of HADHA gene at a referred primer-binding site during pre-diagnostic tests for preimplantation genetic diagnosis.NORMAL FATTY ACID CONCENTRATIONS IN YOUNG CHILDREN WITH PHENYLKETONURIA (PKU).Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrate.Earlier diagnosis and strict diets improve the survival rate and clinical course of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.Triheptanoin versus trioctanoin for long-chain fatty acid oxidation disorders: a double blinded, randomized controlled trial.Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.

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P2860

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

http://www.wikidata.org/entity/Q33617698

description

2003 nî lūn-bûn

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2003 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2003 թվականի հունիսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

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Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

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type

label

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

@ast

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

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prefLabel

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

@ast

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

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Molecular Genetics and Metabolism

P1476

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

@en

P2093

Cary O Harding

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Dietrich Matern

http://www.w3.org/2001/XMLSchema#string

Kaatje Meeuws

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Melanie B Gillingham

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Piero Rinaldo

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Terry Burlingame

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William E Connor

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P2860

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein and amino acids

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey.

Dietary sources of nutrients among US children, 1989-1991.

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2

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79

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10705005

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2813192

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