Overview
Mads Stemmerik practices in Copenhagen, Denmark. Stemmerik is rated as an Experienced expert by MediFind in the treatment of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Their top areas of expertise are Glycogen Storage Disease Type 5, Myoglobinuria Recurrent, Rhabdomyolysis, and Glycogen Storage Disease Type 13.
Their clinical research consists of co-authoring 19 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 Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase 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
- Advanced
- Glycogen Storage Disease Type 13
- Glycogen Storage Disease Type 5Stemmerik isAdvanced. Learn about Glycogen Storage Disease Type 5.
- Myoglobinuria RecurrentStemmerik isAdvanced. Learn about Myoglobinuria Recurrent.
- RhabdomyolysisStemmerik isAdvanced. Learn about Rhabdomyolysis.
- Experienced
- Amyotonia CongenitaStemmerik isExperienced. Learn about Amyotonia Congenita.
- Becker Muscular DystrophyStemmerik isExperienced. Learn about Becker Muscular Dystrophy.
- Duchenne Muscular DystrophyStemmerik isExperienced. Learn about Duchenne Muscular Dystrophy.
- Glutaric Acidemia Type 2Stemmerik isExperienced. Learn about Glutaric Acidemia Type 2.
- Limb-Girdle Muscular DystrophyStemmerik isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency