Overview
Ute Spiekerkoetter practices in Freiburg, Germany. Ms. Spiekerkoetter is rated as an Experienced expert by MediFind in the treatment of Maple Syrup Urine Disease. Her top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Glycogen Storage Disease Type 6, Carnitine Palmitoyltransferase 1 Deficiency, and Carnitine Palmitoyltransferase 2 Deficiency.
Her clinical research consists of co-authoring 97 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Maple Syrup Urine Disease.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Carnitine Palmitoyltransferase 1 DeficiencyMs. Spiekerkoetter isDistinguished. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyMs. Spiekerkoetter isDistinguished. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Glycogen Storage Disease Type 6Ms. Spiekerkoetter isDistinguished. Learn about Glycogen Storage Disease Type 6.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase DeficiencyMs. Spiekerkoetter isDistinguished. Learn about Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.
- Mitochondrial Trifunctional Protein DeficiencyMs. Spiekerkoetter isDistinguished. Learn about Mitochondrial Trifunctional Protein Deficiency.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) DeficiencyMs. Spiekerkoetter isDistinguished. Learn about Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
- Advanced
- Enlarged LiverMs. Spiekerkoetter isAdvanced. Learn about Enlarged Liver.
- Glycogen Storage Disease Type 0Ms. Spiekerkoetter isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Isovaleric AcidemiaMs. Spiekerkoetter isAdvanced. Learn about Isovaleric Acidemia.
- Low Blood SugarMs. Spiekerkoetter isAdvanced. Learn about Low Blood Sugar.
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMs. Spiekerkoetter isAdvanced. Learn about Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
- Methylmalonic AcidemiaMs. Spiekerkoetter isAdvanced. Learn about Methylmalonic Acidemia.
- Experienced
- CardiomyopathyMs. Spiekerkoetter isExperienced. Learn about Cardiomyopathy.
- CholestasisMs. Spiekerkoetter isExperienced. Learn about Cholestasis.
- Chromosome 2 Uniparental DisomyMs. Spiekerkoetter isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- CitrullinemiaMs. Spiekerkoetter isExperienced. Learn about Citrullinemia.
- Fanconi Bickel SyndromeMs. Spiekerkoetter isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMs. Spiekerkoetter isExperienced. Learn about Fanconi Syndrome.