Overview
Jurgen Neesen practices practicing medicine in Vienna, Austria.
Neesen is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Boomerang Dysplasia, Epidermodysplasia Verruciformis, Familial Deafness, and Chromosome 13q Duplication.
They are actively involved in clinical research, co-authoring 29 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 Jurgen Neesen
Is Jurgen Neesen a top-rated expert for Boomerang Dysplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Jurgen Neesen is classified as an Advanced expert for Boomerang Dysplasia, 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 Jurgen Neesen participate in research or clinical trials?
Yes. Jurgen Neesen has published 29 articles and abstracts on conditions like Boomerang Dysplasia. You can view a list of Jurgen Neesen'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
- Boomerang DysplasiaNeesen isAdvanced. Learn about Boomerang Dysplasia.
- Experienced
- AlbinismNeesen isExperienced. Learn about Albinism.
- Brachydactyly Mononen TypeNeesen isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyNeesen isExperienced. Learn about Chondrodystrophy.
- Chromosome 13q DuplicationNeesen isExperienced. Learn about Chromosome 13q Duplication.
- Epidermodysplasia VerruciformisNeesen isExperienced. Learn about Epidermodysplasia Verruciformis.
- Familial DeafnessNeesen isExperienced. Learn about Familial Deafness.
- Hearing LossNeesen isExperienced. Learn about Hearing Loss.
- Hermansky-Pudlak SyndromeNeesen isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Marfan SyndromeNeesen isExperienced. Learn about Marfan Syndrome.
- Oculocutaneous AlbinismNeesen isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1Neesen isExperienced. Learn about Oculocutaneous Albinism Type 1.
- Oculocutaneous Albinism Type 2Neesen isExperienced. Learn about Oculocutaneous Albinism Type 2.
- Platelet Storage Pool Deficiency
- Schwartz-Jampel SyndromeNeesen isExperienced. Learn about Schwartz-Jampel Syndrome.
- Trisomy 13Neesen isExperienced. Learn about Trisomy 13.
- Trisomy 18Neesen isExperienced. Learn about Trisomy 18.
- WartsNeesen isExperienced. Learn about Warts.
- X-Linked Spondyloepiphyseal Dysplasia Tarda