Overview
Stephanie Torre practices practicing medicine in Rouen, France.
Ms. Torre is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Malonyl-CoA Decarboxylase Deficiency, Rhabdomyolysis, Carnitine Palmitoyltransferase 1 Deficiency, and Carnitine Palmitoyltransferase 2 Deficiency.
She is actively involved in clinical research, co-authoring 17 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 Stephanie Torre
Is Stephanie Torre a top-rated expert for Malonyl-CoA Decarboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Stephanie Torre is classified as an Advanced expert for Malonyl-CoA Decarboxylase Deficiency, 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 Stephanie Torre participate in research or clinical trials?
Yes. Stephanie Torre has published 17 articles and abstracts on conditions like Malonyl-CoA Decarboxylase Deficiency. You can view a list of Stephanie Torre'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
- Malonyl-CoA Decarboxylase Deficiency
- Experienced
- Brachydactyly Mononen TypeMs. Torre isExperienced. Learn about Brachydactyly Mononen Type.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- ChoreaMs. Torre isExperienced. Learn about Chorea.
- Epilepsy in ChildrenMs. Torre isExperienced. Learn about Epilepsy in Children.
- GangliosidosisMs. Torre isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMs. Torre isExperienced. Learn about GM1 Gangliosidosis.
- HypotoniaMs. Torre isExperienced. Learn about Hypotonia.
- Leigh SyndromeMs. Torre isExperienced. Learn about Leigh Syndrome.
- Metabolic AcidosisMs. Torre isExperienced. Learn about Metabolic Acidosis.
- MPI-CDGMs. Torre isExperienced. Learn about MPI-CDG.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Propionic AcidemiaMs. Torre isExperienced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Torre isExperienced. Learn about Rhabdomyolysis.
- Zellweger SyndromeMs. Torre isExperienced. Learn about Zellweger Syndrome.