Overview
Benedicte Arnaud-Sudrie practices in Rouen, France. Ms. Arnaud-Sudrie is rated as an Advanced expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Hydrops Fetalis, Fetal Edema, Malonyl-CoA Decarboxylase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
Her clinical research consists of co-authoring 17 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
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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
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyMs. Arnaud-Sudrie isAdvanced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Fetal EdemaMs. Arnaud-Sudrie isAdvanced. Learn about Fetal Edema.
- Hemolytic Disease of the NewbornMs. Arnaud-Sudrie isAdvanced. Learn about Hemolytic Disease of the Newborn.
- Hydrops FetalisMs. Arnaud-Sudrie isAdvanced. Learn about Hydrops Fetalis.
- Malonyl-CoA Decarboxylase DeficiencyMs. Arnaud-Sudrie isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Metabolic AcidosisMs. Arnaud-Sudrie isAdvanced. Learn about Metabolic Acidosis.
- Experienced
- Alpha ThalassemiaMs. Arnaud-Sudrie isExperienced. Learn about Alpha Thalassemia.
- Brachydactyly Mononen TypeMs. Arnaud-Sudrie isExperienced. Learn about Brachydactyly Mononen Type.
- Carnitine Palmitoyltransferase 1 DeficiencyMs. Arnaud-Sudrie isExperienced. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyMs. Arnaud-Sudrie isExperienced. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Cholesteryl Ester Storage DiseaseMs. Arnaud-Sudrie isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Congenital Erythropoietic PorphyriaMs. Arnaud-Sudrie isExperienced. Learn about Congenital Erythropoietic Porphyria.