Overview
Arnaud Bruneel practices in Paris, France. Mr. Bruneel is rated as a Distinguished expert by MediFind in the treatment of MPI-CDG. His top areas of expertise are MPI-CDG, PMM2-Congenital Disorder of Glycosylation, Phosphomannoisomerase Deficiency, and Limb-Girdle Muscular Dystrophy Type 1A.
His clinical research consists of co-authoring 54 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 4 articles in the study of MPI-CDG.
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.
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
- MPI-CDGMr. Bruneel isDistinguished. Learn about MPI-CDG.
- Advanced
- Limb-Girdle Muscular Dystrophy Type 1A
- Phosphomannoisomerase DeficiencyMr. Bruneel isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- PMM2-Congenital Disorder of Glycosylation
- Experienced
- AchondrogenesisMr. Bruneel isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Bruneel isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeMr. Bruneel isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Brachydactyly Mononen TypeMr. Bruneel isExperienced. Learn about Brachydactyly Mononen Type.