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Journal of Inherited Metabolic Disease
|
May 8, 2010
Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening
Ute Spiekerkoetter
Deutsches Arzteblatt International
|
February 10, 2022
Target Diseases for Neonatal Screening in Germany
Ute Spiekerkoetter, Heiko Krude
Molecular Genetics and Metabolism
|
July 20, 2010
ESI-MS/MS measurement of free carnitine and its precursor γ-butyrobetaine in plasma and dried blood spots from patients with organic acidurias and fatty acid oxidation disorders
Sonja Primassin, Ute Spiekerkoetter
Journal of Inherited Metabolic Disease
|
June 10, 2010
Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models
Ute Spiekerkoetter, Philip A Wood
Biochimica Et Biophysica Acta
|
April 19, 2015
Sexual dimorphism of lipid metabolism in very long-chain acyl-CoA dehydrogenase deficient (VLCAD-/-) mice in response to medium-chain triglycerides (MCT)
Sara Tucci, Ulrich Flögel, Ute Spiekerkoetter
The FEBS Journal
|
August 19, 2015
De novo fatty acid biosynthesis and elongation in very long-chain acyl-CoA dehydrogenase-deficient mice supplemented with odd or even medium-chain fatty acids
Sara Tucci, Sidney Behringer, Ute Spiekerkoetter
Molecular Genetics and Metabolism
|
July 28, 2010
Outcome in six patients with mitochondrial trifunctional protein disorders identified by newborn screening
Astrid Sperk, Martina Mueller, Ute Spiekerkoetter
Molecular Genetics and Metabolism
|
October 4, 2011
Hepatic and muscular effects of different dietary fat content in VLCAD deficient mice
Sonja Primassin, Sara Tucci, Ute Spiekerkoetter
The FEBS Journal
|
October 2, 2010
Fasting-induced oxidative stress in very long chain acyl-CoA dehydrogenase-deficient mice
Sara Tucci, Sonja Primassin, Ute Spiekerkoetter
JIMD Reports
|
April 18, 2022
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency
Sarah Catharina Grünert, Matthias Eckenweiler, Ute Spiekerkoetter
Page
of 11
Search research articles
Search
Showing results (1-10 of 110) with videos related to
Sort By:
Page
of 11
Journal of Inherited Metabolic Disease
|
May 8, 2010
Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening
Ute Spiekerkoetter
Deutsches Arzteblatt International
|
February 10, 2022
Target Diseases for Neonatal Screening in Germany
Ute Spiekerkoetter, Heiko Krude
Molecular Genetics and Metabolism
|
July 20, 2010
ESI-MS/MS measurement of free carnitine and its precursor γ-butyrobetaine in plasma and dried blood spots from patients with organic acidurias and fatty acid oxidation disorders
Sonja Primassin, Ute Spiekerkoetter
Journal of Inherited Metabolic Disease
|
June 10, 2010
Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models
Ute Spiekerkoetter, Philip A Wood
Biochimica Et Biophysica Acta
|
April 19, 2015
Sexual dimorphism of lipid metabolism in very long-chain acyl-CoA dehydrogenase deficient (VLCAD-/-) mice in response to medium-chain triglycerides (MCT)
Sara Tucci, Ulrich Flögel, Ute Spiekerkoetter
The FEBS Journal
|
August 19, 2015
De novo fatty acid biosynthesis and elongation in very long-chain acyl-CoA dehydrogenase-deficient mice supplemented with odd or even medium-chain fatty acids
Sara Tucci, Sidney Behringer, Ute Spiekerkoetter
Molecular Genetics and Metabolism
|
July 28, 2010
Outcome in six patients with mitochondrial trifunctional protein disorders identified by newborn screening
Astrid Sperk, Martina Mueller, Ute Spiekerkoetter
Molecular Genetics and Metabolism
|
October 4, 2011
Hepatic and muscular effects of different dietary fat content in VLCAD deficient mice
Sonja Primassin, Sara Tucci, Ute Spiekerkoetter
The FEBS Journal
|
October 2, 2010
Fasting-induced oxidative stress in very long chain acyl-CoA dehydrogenase-deficient mice
Sara Tucci, Sonja Primassin, Ute Spiekerkoetter
JIMD Reports
|
April 18, 2022
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency
Sarah Catharina Grünert, Matthias Eckenweiler, Ute Spiekerkoetter
Page
of 11