Overview
Monique Cordonnier practices practicing medicine in Brussels, Belgium.
Ms. Cordonnier is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Continuous Muscle Fiber Activity Hereditary, Isaacs' Syndrome, X-Linked Congenital Stationary Night Blindness, and Knobloch Syndrome.
She is actively involved in clinical research, co-authoring 20 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 Monique Cordonnier
Is Monique Cordonnier a top-rated expert for Continuous Muscle Fiber Activity Hereditary?
MediFind is an objective health platform that identifies experts based on real-world data. Monique Cordonnier is classified as an Advanced expert for Continuous Muscle Fiber Activity Hereditary, 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 Monique Cordonnier participate in research or clinical trials?
Yes. Monique Cordonnier has published 20 articles and abstracts on conditions like Continuous Muscle Fiber Activity Hereditary. You can view a list of Monique Cordonnier'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
- Continuous Muscle Fiber Activity Hereditary
- Isaacs' SyndromeMs. Cordonnier isAdvanced. Learn about Isaacs' Syndrome.
- X-Linked Congenital Stationary Night Blindness
- Experienced
- AmblyopiaMs. Cordonnier isExperienced. Learn about Amblyopia.
- BlepharophimosisMs. Cordonnier isExperienced. Learn about Blepharophimosis.
- Blue Cone MonochromatismMs. Cordonnier isExperienced. Learn about Blue Cone Monochromatism.
- Brown SyndromeMs. Cordonnier isExperienced. Learn about Brown Syndrome.
- Ciliary Dyskinesia-BronchiectasisMs. Cordonnier isExperienced. Learn about Ciliary Dyskinesia-Bronchiectasis.
- Color BlindnessMs. Cordonnier isExperienced. Learn about Color Blindness.
- DextrocardiaMs. Cordonnier isExperienced. Learn about Dextrocardia.
- Dextrocardia with Situs InversusMs. Cordonnier isExperienced. Learn about Dextrocardia with Situs Inversus.
- EncephaloceleMs. Cordonnier isExperienced. Learn about Encephalocele.
- Eyelid DroopingMs. Cordonnier isExperienced. Learn about Eyelid Drooping.
- Kartagener SyndromeMs. Cordonnier isExperienced. Learn about Kartagener Syndrome.
- Knobloch SyndromeMs. Cordonnier isExperienced. Learn about Knobloch Syndrome.
- NearsightednessMs. Cordonnier isExperienced. Learn about Nearsightedness.
- Retinal DetachmentMs. Cordonnier isExperienced. Learn about Retinal Detachment.
- Situs InversusMs. Cordonnier isExperienced. Learn about Situs Inversus.