Overview
Cecile Acquaviva practices practicing medicine in Lyon, France.
Ms. Acquaviva is highly rated in 7 conditions, according to our data. Her clinical expertise encompasses Primary Hyperoxaluria, Glutaric Acidemia Type 2, Riboflavin Transporter Deficiency Neuronopathy, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Kidney Transplant.
She is actively involved in clinical research, co-authoring 50 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 Cecile E. Acquaviva
Is Cecile E. Acquaviva a top-rated expert for Primary Hyperoxaluria?
MediFind is an objective health platform that identifies experts based on real-world data. Cecile E. Acquaviva is classified as an Distinguished expert for Primary Hyperoxaluria, 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 Cecile E. Acquaviva participate in research or clinical trials?
Yes. Cecile E. Acquaviva has published 50 articles and abstracts on conditions like Primary Hyperoxaluria. You can view a list of Cecile E. Acquaviva'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
- Distinguished
- Primary HyperoxaluriaMs. Acquaviva isDistinguished. Learn about Primary Hyperoxaluria.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Glutaric Acidemia Type 2Ms. Acquaviva isAdvanced. Learn about Glutaric Acidemia Type 2.
- Glycine EncephalopathyMs. Acquaviva isAdvanced. Learn about Glycine Encephalopathy.
- NephrocalcinosisMs. Acquaviva isAdvanced. Learn about Nephrocalcinosis.
- Primary Hyperoxaluria Type 1Ms. Acquaviva isAdvanced. Learn about Primary Hyperoxaluria Type 1.
- Riboflavin Transporter Deficiency Neuronopathy
- Experienced
- Achalasia Microcephaly SyndromeMs. Acquaviva isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acute Cerebellar AtaxiaMs. Acquaviva isExperienced. Learn about Acute Cerebellar Ataxia.
- AnemiaMs. Acquaviva isExperienced. Learn about Anemia.
- CalcinosisMs. Acquaviva isExperienced. Learn about Calcinosis.
- Carnitine Palmitoyltransferase 1 DeficiencyMs. Acquaviva isExperienced. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyMs. Acquaviva isExperienced. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Cerebellar Multiple System AtrophyMs. Acquaviva isExperienced. Learn about Cerebellar Multiple System Atrophy.
- Congenital Hemolytic AnemiaMs. Acquaviva isExperienced. Learn about Congenital Hemolytic Anemia.
- Cortical DysplasiaMs. Acquaviva isExperienced. Learn about Cortical Dysplasia.
- CystinosisMs. Acquaviva isExperienced. Learn about Cystinosis.
- Delayed GrowthMs. Acquaviva isExperienced. Learn about Delayed Growth.
- Drug Induced DyskinesiaMs. Acquaviva isExperienced. Learn about Drug Induced Dyskinesia.
- Enlarged LiverMs. Acquaviva isExperienced. Learn about Enlarged Liver.
- Hearing LossMs. Acquaviva isExperienced. Learn about Hearing Loss.
- HemoglobinopathyMs. Acquaviva isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaMs. Acquaviva isExperienced. Learn about Hemolytic Anemia.
- Hereditary AtaxiaMs. Acquaviva isExperienced. Learn about Hereditary Ataxia.
- Kidney StonesMs. Acquaviva isExperienced. Learn about Kidney Stones.
- Kidney TransplantMs. Acquaviva isExperienced. Learn about Kidney Transplant.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- MalnutritionMs. Acquaviva isExperienced. Learn about Malnutrition.
- Marfan SyndromeMs. Acquaviva isExperienced. Learn about Marfan Syndrome.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Metabolic AcidosisMs. Acquaviva isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaMs. Acquaviva isExperienced. Learn about Methylmalonic Acidemia.
- MicrocephalyMs. Acquaviva isExperienced. Learn about Microcephaly.
- Mitochondrial Complex V DeficiencyMs. Acquaviva isExperienced. Learn about Mitochondrial Complex V Deficiency.
- Mitochondrial Trifunctional Protein Deficiency
- Primary Hyperoxaluria Type 3Ms. Acquaviva isExperienced. Learn about Primary Hyperoxaluria Type 3.
- Primary Lateral SclerosisMs. Acquaviva isExperienced. Learn about Primary Lateral Sclerosis.
- Propionic AcidemiaMs. Acquaviva isExperienced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Acquaviva isExperienced. Learn about Rhabdomyolysis.
- Short Bowel SyndromeMs. Acquaviva isExperienced. Learn about Short Bowel Syndrome.
- Short-Chain Acyl-CoA Dehydrogenase DeficiencyMs. Acquaviva isExperienced. Learn about Short-Chain Acyl-CoA Dehydrogenase Deficiency.
- ThalassemiaMs. Acquaviva isExperienced. Learn about Thalassemia.
- Vitamin B12 Deficiency AnemiaMs. Acquaviva isExperienced. Learn about Vitamin B12 Deficiency Anemia.