Overview
Eric Bieth practices in Toulouse, France. Mr. Bieth is rated as a Distinguished expert by MediFind in the treatment of Congenital Bilateral Absence of the Vas Deferens. His top areas of expertise are Congenital Bilateral Absence of the Vas Deferens, Prader-Willi Syndrome, Chromosome 15q Deletion, and Cystic Fibrosis.
His clinical research consists of co-authoring 75 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 5 articles in the study of Congenital Bilateral Absence of the Vas Deferens.
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
- Congenital Bilateral Absence of the Vas Deferens
- Advanced
- Chromosome 15q DeletionMr. Bieth isAdvanced. Learn about Chromosome 15q Deletion.
- Cystic FibrosisMr. Bieth isAdvanced. Learn about Cystic Fibrosis.
- Prader-Willi SyndromeMr. Bieth isAdvanced. Learn about Prader-Willi Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeMr. Bieth isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acute Cerebellar AtaxiaMr. Bieth isExperienced. Learn about Acute Cerebellar Ataxia.
- ApraxiaMr. Bieth isExperienced. Learn about Apraxia.
- Arthrogryposis Multiplex CongenitaMr. Bieth isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Beckwith-Wiedemann SyndromeMr. Bieth isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia