Overview
Virginie Laurier practices in Hendaye, France. Ms. Laurier is rated as a Distinguished expert by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Prader-Willi Syndrome, Chromosome 15q Deletion, and Familial Hypertriglyceridemia.
Her clinical research consists of co-authoring 22 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 21 articles in the study of Prader-Willi Syndrome.
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
- Prader-Willi SyndromeMs. Laurier isDistinguished. Learn about Prader-Willi Syndrome.
- Advanced
- Chromosome 15q DeletionMs. Laurier isAdvanced. Learn about Chromosome 15q Deletion.
- Experienced
- Familial HypertriglyceridemiaMs. Laurier isExperienced. Learn about Familial Hypertriglyceridemia.