Overview
Audrey Letourneau practices in Lausanne, Switzerland. Ms. Letourneau is highly rated in 3 conditions, according to our data. Her top areas of expertise are Down Syndrome, Angioimmunoblastic T-cell Lymphoma, Large-Cell Immunoblastic Lymphoma, and T-Cell Lymphoma.
Her clinical research consists of co-authoring 44 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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
- Down SyndromeMs. Letourneau isDistinguished. Learn about Down Syndrome.
- Advanced
- Angioimmunoblastic T-cell LymphomaMs. Letourneau isAdvanced. Learn about Angioimmunoblastic T-cell Lymphoma.
- Large-Cell Immunoblastic LymphomaMs. Letourneau isAdvanced. Learn about Large-Cell Immunoblastic Lymphoma.
- Experienced
- Anaplastic Large Cell LymphomaMs. Letourneau isExperienced. Learn about Anaplastic Large Cell Lymphoma.
- Chromosome 13q DuplicationMs. Letourneau isExperienced. Learn about Chromosome 13q Duplication.
- Chromosome 8p DeletionMs. Letourneau isExperienced. Learn about Chromosome 8p Deletion.
- Esophageal AtresiaMs. Letourneau isExperienced. Learn about Esophageal Atresia.
- Gastroesophageal Reflux in InfantsMs. Letourneau isExperienced. Learn about Gastroesophageal Reflux in Infants.
- Glucose Phosphate Isomerase DeficiencyMs. Letourneau isExperienced. Learn about Glucose Phosphate Isomerase Deficiency.