Overview
Veronique Manel practices practicing medicine in Bron, France.
Manel is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Facioscapulohumeral Muscular Dystrophy (FSHD), Lethal Congenital Contracture Syndrome, Chromosome 18p Deletion, and Multiple Mononeuropathy.
They are actively involved in clinical research, co-authoring 25 peer reviewed articles.
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 Veronique Manel
Is Veronique Manel a top-rated expert for Facioscapulohumeral Muscular Dystrophy (FSHD)?
MediFind is an objective health platform that identifies experts based on real-world data. Veronique Manel is classified as an Advanced expert for Facioscapulohumeral Muscular Dystrophy (FSHD), 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 Veronique Manel participate in research or clinical trials?
Yes. Veronique Manel has published 25 articles and abstracts on conditions like Facioscapulohumeral Muscular Dystrophy (FSHD). You can view a list of Veronique Manel'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
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Lethal Congenital Contracture Syndrome
- Experienced
- Accessory Deep Peroneal NerveManel isExperienced. Learn about Accessory Deep Peroneal Nerve.
- Arthrogryposis Multiplex Congenita
- CardiomyopathyManel isExperienced. Learn about Cardiomyopathy.
- Centronuclear MyopathyManel isExperienced. Learn about Centronuclear Myopathy.
- Chromosome 18p DeletionManel isExperienced. Learn about Chromosome 18p Deletion.
- Chronic PolyradiculoneuritisManel isExperienced. Learn about Chronic Polyradiculoneuritis.
- Congenital ContracturesManel isExperienced. Learn about Congenital Contractures.
- Congenital Fiber-Type Disproportion
- Congenital Myasthenic Syndrome
- Dilated Cardiomyopathy (DCM)Manel isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Dominant Dystrophic Epidermolysis Bullosa
- Dowling-Meara Epidermolysis Bullosa Simplex
- Fetal Parvovirus SyndromeManel isExperienced. Learn about Fetal Parvovirus Syndrome.
- Guillain-Barre SyndromeManel isExperienced. Learn about Guillain-Barre Syndrome.
- Hereditary HyperekplexiaManel isExperienced. Learn about Hereditary Hyperekplexia.
- HypotoniaManel isExperienced. Learn about Hypotonia.
- Infant Respiratory Distress Syndrome
- Infantile Axonal NeuropathyManel isExperienced. Learn about Infantile Axonal Neuropathy.
- Multiple MononeuropathyManel isExperienced. Learn about Multiple Mononeuropathy.
- Parvovirus Antenatal Infection
- Primary Lateral SclerosisManel isExperienced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)Manel isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 1
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Tubular Aggregate MyopathyManel isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyManel isExperienced. Learn about X-Linked Myotubular Myopathy.