Overview
Apolline Imbard practices practicing medicine in Gif-sur-yvette, France.
Ms. Imbard is highly rated in 13 conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Carnitine Palmitoyltransferase 1 Deficiency, Carnitine Palmitoyltransferase 2 Deficiency, and Homocystinuria.
She is actively involved in clinical research, co-authoring 56 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 Apolline Imbard
Is Apolline Imbard a top-rated expert for Propionic Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Apolline Imbard is classified as an Advanced expert for Propionic Acidemia, 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 Apolline Imbard participate in research or clinical trials?
Yes. Apolline Imbard has published 56 articles and abstracts on conditions like Propionic Acidemia. You can view a list of Apolline Imbard'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
- Arginase DeficiencyMs. Imbard isAdvanced. Learn about Arginase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Carnitine-Acylcarnitine Translocase Deficiency
- HomocystinuriaMs. Imbard isAdvanced. Learn about Homocystinuria.
- HypermethioninemiaMs. Imbard isAdvanced. Learn about Hypermethioninemia.
- Lactic AcidosisMs. Imbard isAdvanced. Learn about Lactic Acidosis.
- Maple Syrup Urine DiseaseMs. Imbard isAdvanced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaMs. Imbard isAdvanced. Learn about Methylmalonic Acidemia.
- Propionic AcidemiaMs. Imbard isAdvanced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Imbard isAdvanced. Learn about Rhabdomyolysis.
- Urea Cycle Disorders (UCD)Ms. Imbard isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Vitamin B12 Deficiency AnemiaMs. Imbard isAdvanced. Learn about Vitamin B12 Deficiency Anemia.
- Experienced
- Biotinidase DeficiencyMs. Imbard isExperienced. Learn about Biotinidase Deficiency.
- CACH SyndromeMs. Imbard isExperienced. Learn about CACH Syndrome.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Congenital Hemolytic AnemiaMs. Imbard isExperienced. Learn about Congenital Hemolytic Anemia.
- Enlarged LiverMs. Imbard isExperienced. Learn about Enlarged Liver.
- EpilepsyMs. Imbard isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenMs. Imbard isExperienced. Learn about Epilepsy in Children.
- Fifth DiseaseMs. Imbard isExperienced. Learn about Fifth Disease.
- Hemolytic AnemiaMs. Imbard isExperienced. Learn about Hemolytic Anemia.
- Homocystinuria due to MTHFR DeficiencyMs. Imbard isExperienced. Learn about Homocystinuria due to MTHFR Deficiency.
- Inborn Amino Acid Metabolism DisorderMs. Imbard isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Lysinuric Protein IntoleranceMs. Imbard isExperienced. Learn about Lysinuric Protein Intolerance.
- MalabsorptionMs. Imbard isExperienced. Learn about Malabsorption.
- MalnutritionMs. Imbard isExperienced. Learn about Malnutrition.
- Metabolic AcidosisMs. Imbard isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic Acidemia with Homocystinuria
- Multiple Carboxylase DeficiencyMs. Imbard isExperienced. Learn about Multiple Carboxylase Deficiency.
- Parvovirus Antenatal InfectionMs. Imbard isExperienced. Learn about Parvovirus Antenatal Infection.
- Phenylketonuria (PKU)Ms. Imbard isExperienced. Learn about Phenylketonuria (PKU).
- Prolidase DeficiencyMs. Imbard isExperienced. Learn about Prolidase Deficiency.
- Pyridoxine DeficiencyMs. Imbard isExperienced. Learn about Pyridoxine Deficiency.
- SeizuresMs. Imbard isExperienced. Learn about Seizures.
- Short Bowel SyndromeMs. Imbard isExperienced. Learn about Short Bowel Syndrome.
- TonsillitisMs. Imbard isExperienced. Learn about Tonsillitis.
- Transient Erythroblastopenia of Childhood
- Tyrosinemia Type 1Ms. Imbard isExperienced. Learn about Tyrosinemia Type 1.