Overview
Ulrike Mutze practices practicing medicine in Heidelberg, Germany.
Ms. Mutze is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Isovaleric Acidemia, Vitamin B12 Deficiency, Vitamin B12 Deficiency Anemia, and Homocystinuria due to MTHFR Deficiency.
She is actively involved in clinical research, co-authoring 61 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 Ulrike Mutze
Is Ulrike Mutze a top-rated expert for Isovaleric Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Ulrike Mutze is classified as an Elite expert for Isovaleric Acidemia, 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 Ulrike Mutze participate in research or clinical trials?
Yes. Ulrike Mutze has published 61 articles and abstracts on conditions like Isovaleric Acidemia. You can view a list of Ulrike Mutze'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
- Elite
- Isovaleric AcidemiaMs. Mutze isElite. Learn about Isovaleric Acidemia.
- Distinguished
- Vitamin B12 DeficiencyMs. Mutze isDistinguished. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Mutze isDistinguished. Learn about Vitamin B12 Deficiency Anemia.
- Advanced
- Glutaric Acidemia Type 1Ms. Mutze isAdvanced. Learn about Glutaric Acidemia Type 1.
- HomocystinuriaMs. Mutze isAdvanced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR Deficiency
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseMs. Mutze isAdvanced. Learn about Maple Syrup Urine Disease.
- Mitochondrial Trifunctional Protein Deficiency
- Phenylketonuria (PKU)Ms. Mutze isAdvanced. Learn about Phenylketonuria (PKU).
- Propionic AcidemiaMs. Mutze isAdvanced. Learn about Propionic Acidemia.
- Sialic Acid Storage DiseaseMs. Mutze isAdvanced. Learn about Sialic Acid Storage Disease.
- SialuriaMs. Mutze isAdvanced. Learn about Sialuria.
- Urea Cycle Disorders (UCD)Ms. Mutze isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Experienced
- Arginase DeficiencyMs. Mutze isExperienced. Learn about Arginase Deficiency.
- Argininosuccinic AciduriaMs. Mutze isExperienced. Learn about Argininosuccinic Aciduria.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Benign Familial Neonatal SeizuresMs. Mutze isExperienced. Learn about Benign Familial Neonatal Seizures.
- Brachydactyly Mononen TypeMs. Mutze isExperienced. Learn about Brachydactyly Mononen Type.
- EpilepsyMs. Mutze isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenMs. Mutze isExperienced. Learn about Epilepsy in Children.
- GangliosidosisMs. Mutze isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMs. Mutze isExperienced. Learn about GM1 Gangliosidosis.
- Low Blood SugarMs. Mutze isExperienced. Learn about Low Blood Sugar.
- MalnutritionMs. Mutze isExperienced. Learn about Malnutrition.
- Maternal HyperphenylalaninemiaMs. Mutze isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaMs. Mutze isExperienced. Learn about Methylmalonic Acidemia.
- Mucolipidosis 3Ms. Mutze isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Mutze isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Neonatal SepsisMs. Mutze isExperienced. Learn about Neonatal Sepsis.
- Newborn Low Blood SugarMs. Mutze isExperienced. Learn about Newborn Low Blood Sugar.
- RhabdomyolysisMs. Mutze isExperienced. Learn about Rhabdomyolysis.
- SialidosisMs. Mutze isExperienced. Learn about Sialidosis.
- Smith-Lemli-Opitz SyndromeMs. Mutze isExperienced. Learn about Smith-Lemli-Opitz Syndrome.
- SpasticityMs. Mutze isExperienced. Learn about Spasticity.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency