Overview
Johan Den Dunnen practices practicing medicine in Leiden, Netherlands.
Mr. Den Dunnen is highly rated in 1 condition, according to our data. His clinical expertise encompasses Congenital Muscular Dystrophy Type 1A, Micrognathia, Optic Nerve Atrophy, and Duchenne Muscular Dystrophy.
He is actively involved in clinical research, co-authoring 106 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 Johan T. Den Dunnen
Is Johan T. Den Dunnen a top-rated expert for Congenital Muscular Dystrophy Type 1A?
MediFind is an objective health platform that identifies experts based on real-world data. Johan T. Den Dunnen is classified as an Advanced expert for Congenital Muscular Dystrophy Type 1A, 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 Johan T. Den Dunnen participate in research or clinical trials?
Yes. Johan T. Den Dunnen has published 106 articles and abstracts on conditions like Congenital Muscular Dystrophy Type 1A. You can view a list of Johan T. Den Dunnen'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
- Congenital Muscular Dystrophy Type 1AMr. Den Dunnen isAdvanced. Learn about Congenital Muscular Dystrophy Type 1A.
- Experienced
- Autosomal Dominant Polycystic Kidney DiseaseMr. Den Dunnen isExperienced. Learn about Autosomal Dominant Polycystic Kidney Disease.
- Becker Muscular DystrophyMr. Den Dunnen isExperienced. Learn about Becker Muscular Dystrophy.
- Coffin-Siris SyndromeMr. Den Dunnen isExperienced. Learn about Coffin-Siris Syndrome.
- Duchenne Muscular DystrophyMr. Den Dunnen isExperienced. Learn about Duchenne Muscular Dystrophy.
- Familial Adenomatous PolyposisMr. Den Dunnen isExperienced. Learn about Familial Adenomatous Polyposis.
- Genital DwarfismMr. Den Dunnen isExperienced. Learn about Genital Dwarfism.
- Huntington DiseaseMr. Den Dunnen isExperienced. Learn about Huntington Disease.
- HypotoniaMr. Den Dunnen isExperienced. Learn about Hypotonia.
- Leukocyte Adhesion Deficiency Type 1Mr. Den Dunnen isExperienced. Learn about Leukocyte Adhesion Deficiency Type 1.
- MicrognathiaMr. Den Dunnen isExperienced. Learn about Micrognathia.
- Miller SyndromeMr. Den Dunnen isExperienced. Learn about Miller Syndrome.
- Optic Nerve AtrophyMr. Den Dunnen isExperienced. Learn about Optic Nerve Atrophy.
- Polycystic Kidney DiseaseMr. Den Dunnen isExperienced. Learn about Polycystic Kidney Disease.
- Russell-Silver DwarfismMr. Den Dunnen isExperienced. Learn about Russell-Silver Dwarfism.