Overview
Uta Matysiak practices practicing medicine in Freiburg, Germany.
Ms. Matysiak is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Spondyloepimetaphyseal Dysplasia Strudwick Type, 3M Syndrome, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, and Chromosome 2 Uniparental Disomy.
She is actively involved in clinical research, co-authoring 13 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 Uta Matysiak
Is Uta Matysiak a top-rated expert for Spondyloepimetaphyseal Dysplasia Strudwick Type?
MediFind is an objective health platform that identifies experts based on real-world data. Uta Matysiak is classified as an Advanced expert for Spondyloepimetaphyseal Dysplasia Strudwick Type, 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 Uta Matysiak participate in research or clinical trials?
Yes. Uta Matysiak has published 13 articles and abstracts on conditions like Spondyloepimetaphyseal Dysplasia Strudwick Type. You can view a list of Uta Matysiak'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
- 3M SyndromeMs. Matysiak isAdvanced. Learn about 3M Syndrome.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Spondyloepimetaphyseal Dysplasia Strudwick Type
- Experienced
- AchondrogenesisMs. Matysiak isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMs. Matysiak isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeMs. Matysiak isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- AniridiaMs. Matysiak isExperienced. Learn about Aniridia.
- BowlegsMs. Matysiak isExperienced. Learn about Bowlegs.
- Chromosome 2 Uniparental DisomyMs. Matysiak isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- HypotoniaMs. Matysiak isExperienced. Learn about Hypotonia.
- Increased Head CircumferenceMs. Matysiak isExperienced. Learn about Increased Head Circumference.
- Knock KneesMs. Matysiak isExperienced. Learn about Knock Knees.
- MicrognathiaMs. Matysiak isExperienced. Learn about Micrognathia.
- Pierre Robin SequenceMs. Matysiak isExperienced. Learn about Pierre Robin Sequence.
- Russell-Silver DwarfismMs. Matysiak isExperienced. Learn about Russell-Silver Dwarfism.
- ScoliosisMs. Matysiak isExperienced. Learn about Scoliosis.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency