Overview
Friederike Horster practices in Heidelberg, Germany. Horster is rated as a Distinguished expert by MediFind in the treatment of Methylmalonyl Coenzyme A Mutase Deficiency. Their top areas of expertise are Propionic Acidemia, Methylmalonic Acidemia, Methylmalonyl Coenzyme A Mutase Deficiency, Mohr-Tranebjaerg Syndrome, and Kidney Transplant.
Their clinical research consists of co-authoring 29 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of Methylmalonyl Coenzyme A Mutase Deficiency.
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
- Methylmalonic AcidemiaHorster isDistinguished. Learn about Methylmalonic Acidemia.
- Methylmalonyl Coenzyme A Mutase Deficiency
- Propionic AcidemiaHorster isDistinguished. Learn about Propionic Acidemia.
- Advanced
- Argininosuccinic AciduriaHorster isAdvanced. Learn about Argininosuccinic Aciduria.
- Mohr-Tranebjaerg SyndromeHorster isAdvanced. Learn about Mohr-Tranebjaerg Syndrome.
- Experienced
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Chronic Kidney DiseaseHorster isExperienced. Learn about Chronic Kidney Disease.
- Glutaric Acidemia Type 1Horster isExperienced. Learn about Glutaric Acidemia Type 1.
- HomocystinuriaHorster isExperienced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR Deficiency
- Inborn Amino Acid Metabolism Disorder