Ute Spiekerkoetter

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 13 publications

Current issues regarding treatment of mitochondrial fatty acid oxidation disorders.

Current issues regarding treatment of mitochondrial fatty acid oxidation disorders.

Journal: Journal of inherited metabolic disease

Published: April 20, 2010

Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models.

Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models.

Journal: Journal of inherited metabolic disease

Published: November 04, 2009

Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.

Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.

Journal: Journal of inherited metabolic disease

Published: October 24, 2009

Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.

Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.

Journal: Journal of inherited metabolic disease

Published: December 29, 2008

Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

Journal: Journal of inherited metabolic disease

Published: December 29, 2008

Effects of a fat load and exercise on asymptomatic VLCAD deficiency.

Effects of a fat load and exercise on asymptomatic VLCAD deficiency.

Journal: Journal of inherited metabolic disease

Published: December 29, 2006

Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient mice.

Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient mice.

Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

Published: November 01, 2006

Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice.

Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice.

Journal: Pediatric research

Published: March 19, 2005

The early-onset phenotype of mitochondrial trifunctional protein deficiency: a lethal disorder with multiple tissue involvement.

The early-onset phenotype of mitochondrial trifunctional protein deficiency: a lethal disorder with multiple tissue involvement.

Journal: Journal of inherited metabolic disease

Published: July 13, 2004

Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress.

Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress.

Journal: European journal of clinical investigation

Published: March 18, 2004

Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein.

Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein.

Journal: Muscle & nerve

Published: December 25, 2003

General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover.

General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover.

Journal: Pediatric research

Published: November 25, 2003

Showing 1-12 of 13

Last Updated: 09/26/2026