Overview
Kenji Watanabe practices practicing medicine in Kagoshima, Japan.
Mr. Watanabe is highly rated in 1 condition, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Rhabdomyolysis, Common Cold, and Platelet Storage Pool Deficiency.
He is actively involved in clinical research, co-authoring 8 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 Kenji Watanabe
Is Kenji Watanabe a top-rated expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Kenji Watanabe is classified as an Distinguished expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) 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 Kenji Watanabe participate in research or clinical trials?
Yes. Kenji Watanabe has published 8 articles and abstracts on conditions like Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. You can view a list of Kenji Watanabe'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
- Distinguished
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- AlbinismMr. Watanabe isExperienced. Learn about Albinism.
- Common ColdMr. Watanabe isExperienced. Learn about Common Cold.
- Hermansky-Pudlak SyndromeMr. Watanabe isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Low Blood SugarMr. Watanabe isExperienced. Learn about Low Blood Sugar.
- Oculocutaneous AlbinismMr. Watanabe isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1Mr. Watanabe isExperienced. Learn about Oculocutaneous Albinism Type 1.
- Oculocutaneous Albinism Type 2Mr. Watanabe isExperienced. Learn about Oculocutaneous Albinism Type 2.
- Platelet Storage Pool DeficiencyMr. Watanabe isExperienced. Learn about Platelet Storage Pool Deficiency.
- PseudoachondroplasiaMr. Watanabe isExperienced. Learn about Pseudoachondroplasia.
- RhabdomyolysisMr. Watanabe isExperienced. Learn about Rhabdomyolysis.