Overview
Ute Spiekerkoetter practices practicing medicine in Freiburg, Germany.
Ms. Spiekerkoetter is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Glycogen Storage Disease Type 6, Mitochondrial Trifunctional Protein Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, and Carnitine Palmitoyltransferase 2 Deficiency.
She is actively involved in clinical research, co-authoring 92 peer reviewed articles.
Gender
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.
Frequently Asked Questions about Ute Spiekerkoetter
Is Ute Spiekerkoetter a top-rated expert for Glycogen Storage Disease Type 6?
MediFind is an objective health platform that identifies experts based on real-world data. Ute Spiekerkoetter is classified as an Distinguished expert for Glycogen Storage Disease Type 6, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Ute Spiekerkoetter participate in research or clinical trials?
Yes. Ute Spiekerkoetter has published 92 articles and abstracts on conditions like Glycogen Storage Disease Type 6. You can view a list of Ute Spiekerkoetter's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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.
- Phenylketonuria (PKU)Ms. Spiekerkoetter isAdvanced. Learn about Phenylketonuria (PKU).
- Propionic AcidemiaMs. Spiekerkoetter isAdvanced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Spiekerkoetter isAdvanced. Learn about Rhabdomyolysis.
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
- Urea Cycle Disorders (UCD)Ms. Spiekerkoetter isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Vitamin B12 DeficiencyMs. Spiekerkoetter isAdvanced. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Spiekerkoetter isAdvanced. Learn about Vitamin B12 Deficiency Anemia.
- Von Gierke DiseaseMs. Spiekerkoetter isAdvanced. Learn about Von Gierke Disease.
- 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.
- Farber LipogranulomatosisMs. Spiekerkoetter isExperienced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseMs. Spiekerkoetter isExperienced. Learn about Gaucher Disease.
- Glutaric Acidemia Type 2Ms. Spiekerkoetter isExperienced. Learn about Glutaric Acidemia Type 2.
- HeartburnMs. Spiekerkoetter isExperienced. Learn about Heartburn.
- HomocystinuriaMs. Spiekerkoetter isExperienced. Learn about Homocystinuria.
- HypothyroidismMs. Spiekerkoetter isExperienced. Learn about Hypothyroidism.
- Increased Head CircumferenceMs. Spiekerkoetter isExperienced. Learn about Increased Head Circumference.
- Infant HyperglycemiaMs. Spiekerkoetter isExperienced. Learn about Infant Hyperglycemia.
- Infantile Axonal NeuropathyMs. Spiekerkoetter isExperienced. Learn about Infantile Axonal Neuropathy.
- MalnutritionMs. Spiekerkoetter isExperienced. Learn about Malnutrition.
- Maple Syrup Urine DiseaseMs. Spiekerkoetter isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaMs. Spiekerkoetter isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Metabolic AcidosisMs. Spiekerkoetter isExperienced. Learn about Metabolic Acidosis.
- MicrognathiaMs. Spiekerkoetter isExperienced. Learn about Micrognathia.
- Neonatal HypothyroidismMs. Spiekerkoetter isExperienced. Learn about Neonatal Hypothyroidism.
- Newborn Low Blood SugarMs. Spiekerkoetter isExperienced. Learn about Newborn Low Blood Sugar.
- Pierre Robin SequenceMs. Spiekerkoetter isExperienced. Learn about Pierre Robin Sequence.
- PMM2-Congenital Disorder of GlycosylationMs. Spiekerkoetter isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Primary Carnitine DeficiencyMs. Spiekerkoetter isExperienced. Learn about Primary Carnitine Deficiency.
- Protein DeficiencyMs. Spiekerkoetter isExperienced. Learn about Protein Deficiency.
- Riboflavin Transporter Deficiency NeuronopathyMs. Spiekerkoetter isExperienced. Learn about Riboflavin Transporter Deficiency Neuronopathy.
- Russell-Silver DwarfismMs. Spiekerkoetter isExperienced. Learn about Russell-Silver Dwarfism.