Overview
Francois Labarthe practices practicing medicine in Tours, France.
Mr. Labarthe is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Primary Carnitine Deficiency, Phenylketonuria (PKU), Pompe Disease, and Mucopolysaccharidoses (MPS).
He is actively involved in clinical research, co-authoring 72 peer reviewed articles and participating in 3 clinical trials.
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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.
3 Clinical Trials
Frequently Asked Questions about Francois Labarthe
Is Francois Labarthe a top-rated expert for Primary Carnitine Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Francois Labarthe is classified as an Distinguished expert for Primary Carnitine 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 Francois Labarthe participate in research or clinical trials?
Yes. Francois Labarthe has published 72 articles and abstracts on conditions like Primary Carnitine Deficiency. You can view a list of Francois Labarthe'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 Carnitine DeficiencyMr. Labarthe isDistinguished. Learn about Primary Carnitine Deficiency.
- Advanced
- Beta-Ketothiolase DeficiencyMr. Labarthe isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Mucopolysaccharidoses (MPS)Mr. Labarthe isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Phenylketonuria (PKU)Mr. Labarthe isAdvanced. Learn about Phenylketonuria (PKU).
- Pompe DiseaseMr. Labarthe isAdvanced. Learn about Pompe Disease.
- Experienced
- Barth SyndromeMr. Labarthe isExperienced. Learn about Barth Syndrome.
- Brachydactyly Mononen TypeMr. Labarthe isExperienced. Learn about Brachydactyly Mononen Type.
- CardiomyopathyMr. Labarthe isExperienced. Learn about Cardiomyopathy.
- Congenital HypothyroidismMr. Labarthe isExperienced. Learn about Congenital Hypothyroidism.
- Enlarged LiverMr. Labarthe isExperienced. Learn about Enlarged Liver.
- Fructose-1,6-Bisphosphatase DeficiencyMr. Labarthe isExperienced. Learn about Fructose-1,6-Bisphosphatase Deficiency.
- GangliosidosisMr. Labarthe isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMr. Labarthe isExperienced. Learn about GM1 Gangliosidosis.
- Heart FailureMr. Labarthe isExperienced. Learn about Heart Failure.
- Hereditary Fructose IntoleranceMr. Labarthe isExperienced. Learn about Hereditary Fructose Intolerance.
- High Blood Pressure in InfantsMr. Labarthe isExperienced. Learn about High Blood Pressure in Infants.
- HistiocytosisMr. Labarthe isExperienced. Learn about Histiocytosis.
- HomocystinuriaMr. Labarthe isExperienced. Learn about Homocystinuria.
- Liver FailureMr. Labarthe isExperienced. Learn about Liver Failure.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Low Blood SugarMr. Labarthe isExperienced. Learn about Low Blood Sugar.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Metabolic AcidosisMr. Labarthe isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaMr. Labarthe isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Trifunctional Protein Deficiency
- MPI-CDGMr. Labarthe isExperienced. Learn about MPI-CDG.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Niemann-Pick DiseaseMr. Labarthe isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMr. Labarthe isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- PericarditisMr. Labarthe isExperienced. Learn about Pericarditis.
- PMM2-Congenital Disorder of GlycosylationMr. Labarthe isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Propionic AcidemiaMr. Labarthe isExperienced. Learn about Propionic Acidemia.
- ReticulohistiocytomaMr. Labarthe isExperienced. Learn about Reticulohistiocytoma.
- RhabdomyolysisMr. Labarthe isExperienced. Learn about Rhabdomyolysis.
- Ventricular FibrillationMr. Labarthe isExperienced. Learn about Ventricular Fibrillation.