Overview
Udo Koehler practices practicing medicine in Munich, Germany.
Koehler is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Platelet Storage Pool Deficiency, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism Type 2, and Hermansky-Pudlak Syndrome.
They are actively involved in clinical research, co-authoring 24 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 Udo Koehler
Is Udo Koehler a top-rated expert for Platelet Storage Pool Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Udo Koehler is classified as an Advanced expert for Platelet Storage Pool Deficiency, 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 Udo Koehler participate in research or clinical trials?
Yes. Udo Koehler has published 24 articles and abstracts on conditions like Platelet Storage Pool Deficiency. You can view a list of Udo Koehler'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
- Platelet Storage Pool Deficiency
- Experienced
- AlbinismKoehler isExperienced. Learn about Albinism.
- Blood ClotsKoehler isExperienced. Learn about Blood Clots.
- Brachial PlexopathyKoehler isExperienced. Learn about Brachial Plexopathy.
- Brachydactyly Mononen TypeKoehler isExperienced. Learn about Brachydactyly Mononen Type.
- Chromosome 5q DuplicationKoehler isExperienced. Learn about Chromosome 5q Duplication.
- Chromosome 7p DuplicationKoehler isExperienced. Learn about Chromosome 7p Duplication.
- Familial Adenomatous PolyposisKoehler isExperienced. Learn about Familial Adenomatous Polyposis.
- Hereditary Neuralgic AmyotrophyKoehler isExperienced. Learn about Hereditary Neuralgic Amyotrophy.
- Hermansky-Pudlak SyndromeKoehler isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Hypomelanotic DisorderKoehler isExperienced. Learn about Hypomelanotic Disorder.
- Oculocutaneous AlbinismKoehler isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1Koehler isExperienced. Learn about Oculocutaneous Albinism Type 1.
- Oculocutaneous Albinism Type 2Koehler isExperienced. Learn about Oculocutaneous Albinism Type 2.
- Potocki-Lupski SyndromeKoehler isExperienced. Learn about Potocki-Lupski Syndrome.
- Smith-Magenis SyndromeKoehler isExperienced. Learn about Smith-Magenis Syndrome.
- Trisomy 17 MosaicismKoehler isExperienced. Learn about Trisomy 17 Mosaicism.