Overview
Elisabeth Mazoyer practices practicing medicine in Bobigny, France.
Her clinical expertise encompasses Dysfibrinogenemia, Familial Hypofibrinogenemia, and Congenital Afibrinogenemia.
She is actively involved in clinical research, co-authoring 9 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 Elisabeth Mazoyer
Is Elisabeth Mazoyer a top-rated expert for Dysfibrinogenemia?
MediFind is an objective health platform that identifies experts based on real-world data. Elisabeth Mazoyer is classified as an Experienced expert for Dysfibrinogenemia, 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 Elisabeth Mazoyer participate in research or clinical trials?
Yes. Elisabeth Mazoyer has published 9 articles and abstracts on conditions like Dysfibrinogenemia. You can view a list of Elisabeth Mazoyer'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
- Experienced
- Congenital AfibrinogenemiaMs. Mazoyer isExperienced. Learn about Congenital Afibrinogenemia.
- DysfibrinogenemiaMs. Mazoyer isExperienced. Learn about Dysfibrinogenemia.
- Familial HypofibrinogenemiaMs. Mazoyer isExperienced. Learn about Familial Hypofibrinogenemia.