Overview
Cecile Bourdain-Acquaviva practices in Bron, France. Ms. Bourdain-Acquaviva is rated as an Experienced expert by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. Her top areas of expertise are Primary Hyperoxaluria Type 1, Primary Hyperoxaluria, Glutaric Acidemia Type 2, Nephrocalcinosis, and Kidney Transplant.
Her clinical research consists of co-authoring 48 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 Carnitine Palmitoyltransferase 2 Deficiency.
Locations
Bron, France
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
- Glutaric Acidemia Type 2Ms. Bourdain-Acquaviva isDistinguished. Learn about Glutaric Acidemia Type 2.
- NephrocalcinosisMs. Bourdain-Acquaviva isDistinguished. Learn about Nephrocalcinosis.
- Primary HyperoxaluriaMs. Bourdain-Acquaviva isDistinguished. Learn about Primary Hyperoxaluria.
- Primary Hyperoxaluria Type 1Ms. Bourdain-Acquaviva isDistinguished. Learn about Primary Hyperoxaluria Type 1.
- Advanced
- Beta-Ketothiolase DeficiencyMs. Bourdain-Acquaviva isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- CystinosisMs. Bourdain-Acquaviva isAdvanced. Learn about Cystinosis.
- Metabolic AcidosisMs. Bourdain-Acquaviva isAdvanced. Learn about Metabolic Acidosis.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyMs. Bourdain-Acquaviva isExperienced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Andersen DiseaseMs. Bourdain-Acquaviva isExperienced. Learn about Andersen Disease.
- Arthrogryposis Multiplex CongenitaMs. Bourdain-Acquaviva isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Arthrogryposis Multiplex Congenita Neurogenic TypeMs. Bourdain-Acquaviva isExperienced. Learn about Arthrogryposis Multiplex Congenita Neurogenic Type.
- CalcinosisMs. Bourdain-Acquaviva isExperienced. Learn about Calcinosis.
- Carnitine Palmitoyltransferase 1 DeficiencyMs. Bourdain-Acquaviva isExperienced. Learn about Carnitine Palmitoyltransferase 1 Deficiency.