Overview
Nathalie Seta practices practicing medicine in Paris, France.
Ms. Seta is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation, Lissencephaly, ALG3-CDG, and Fukuyama Type Muscular Dystrophy.
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 Nathalie Seta
Is Nathalie Seta a top-rated expert for PMM2-Congenital Disorder of Glycosylation?
MediFind is an objective health platform that identifies experts based on real-world data. Nathalie Seta is classified as an Advanced expert for PMM2-Congenital Disorder of Glycosylation, 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 Nathalie Seta participate in research or clinical trials?
Yes. Nathalie Seta has published 50 articles and abstracts on conditions like PMM2-Congenital Disorder of Glycosylation. You can view a list of Nathalie Seta'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
- ALG3-CDGMs. Seta isAdvanced. Learn about ALG3-CDG.
- Fukuyama Type Muscular Dystrophy
- LissencephalyMs. Seta isAdvanced. Learn about Lissencephaly.
- Lissencephaly 2Ms. Seta isAdvanced. Learn about Lissencephaly 2.
- PMM2-Congenital Disorder of Glycosylation
- Walker-Warburg SyndromeMs. Seta isAdvanced. Learn about Walker-Warburg Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeMs. Seta isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acromicric DysplasiaMs. Seta isExperienced. Learn about Acromicric Dysplasia.
- Brachydactyly Mononen TypeMs. Seta isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMs. Seta isExperienced. Learn about Chondrodystrophy.
- Cortical DysplasiaMs. Seta isExperienced. Learn about Cortical Dysplasia.
- Cramp-Fasciculation SyndromeMs. Seta isExperienced. Learn about Cramp-Fasciculation Syndrome.
- Drug Induced DyskinesiaMs. Seta isExperienced. Learn about Drug Induced Dyskinesia.
- Epilepsy in ChildrenMs. Seta isExperienced. Learn about Epilepsy in Children.
- Grass AllergyMs. Seta isExperienced. Learn about Grass Allergy.
- High Blood Pressure in InfantsMs. Seta isExperienced. Learn about High Blood Pressure in Infants.
- HypotoniaMs. Seta isExperienced. Learn about Hypotonia.
- Limb-Girdle Muscular DystrophyMs. Seta isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Limb-Girdle Muscular Dystrophy Type 1A
- MacroglossiaMs. Seta isExperienced. Learn about Macroglossia.
- MicrocephalyMs. Seta isExperienced. Learn about Microcephaly.
- MPI-CDGMs. Seta isExperienced. Learn about MPI-CDG.
- Niemann-Pick DiseaseMs. Seta isExperienced. Learn about Niemann-Pick Disease.
- PericarditisMs. Seta isExperienced. Learn about Pericarditis.
- Schwartz-Jampel SyndromeMs. Seta isExperienced. Learn about Schwartz-Jampel Syndrome.
- TMEM165-CDGMs. Seta isExperienced. Learn about TMEM165-CDG.
- Wilson DiseaseMs. Seta isExperienced. Learn about Wilson Disease.
- X-Linked Retinal DysplasiaMs. Seta isExperienced. Learn about X-Linked Retinal Dysplasia.
- X-Linked Spondyloepiphyseal Dysplasia Tarda