Overview
Michaela Drogemuller practices practicing medicine in Bern, Switzerland.
Ms. Drogemuller is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Cerebellar Hypoplasia, Bernard-Soulier Syndrome, Leigh Syndrome, and Batten Disease.
She is actively involved in clinical research, co-authoring 39 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 Michaela Drogemuller
Is Michaela Drogemuller a top-rated expert for Cerebellar Hypoplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Michaela Drogemuller is classified as an Advanced expert for Cerebellar Hypoplasia, 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 Michaela Drogemuller participate in research or clinical trials?
Yes. Michaela Drogemuller has published 39 articles and abstracts on conditions like Cerebellar Hypoplasia. You can view a list of Michaela Drogemuller'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
- Advanced
- Cerebellar HypoplasiaMs. Drogemuller isAdvanced. Learn about Cerebellar Hypoplasia.
- Experienced
- Autosomal Dominant Polycystic Kidney DiseaseMs. Drogemuller isExperienced. Learn about Autosomal Dominant Polycystic Kidney Disease.
- Batten DiseaseMs. Drogemuller isExperienced. Learn about Batten Disease.
- Bernard-Soulier SyndromeMs. Drogemuller isExperienced. Learn about Bernard-Soulier Syndrome.
- CACH SyndromeMs. Drogemuller isExperienced. Learn about CACH Syndrome.
- ChondrodystrophyMs. Drogemuller isExperienced. Learn about Chondrodystrophy.
- CLN1 DiseaseMs. Drogemuller isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Drogemuller isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Drogemuller isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Drogemuller isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Drogemuller isExperienced. Learn about CLN5 Disease.
- Familial Dilated CardiomyopathyMs. Drogemuller isExperienced. Learn about Familial Dilated Cardiomyopathy.
- Familial HypertriglyceridemiaMs. Drogemuller isExperienced. Learn about Familial Hypertriglyceridemia.
- Hairy Cell Leukemia (HCL)Ms. Drogemuller isExperienced. Learn about Hairy Cell Leukemia (HCL).
- Leigh SyndromeMs. Drogemuller isExperienced. Learn about Leigh Syndrome.
- Limb-Girdle Muscular DystrophyMs. Drogemuller isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- MalabsorptionMs. Drogemuller isExperienced. Learn about Malabsorption.
- Polycystic Kidney DiseaseMs. Drogemuller isExperienced. Learn about Polycystic Kidney Disease.
- Vitamin B12 Deficiency AnemiaMs. Drogemuller isExperienced. Learn about Vitamin B12 Deficiency Anemia.