Overview
Hideaki Sawai practices in Kyoto, Japan. Sawai is highly rated in 7 conditions, according to our data. Their top areas of expertise are Thanatophoric Dysplasia, Acromicric Dysplasia, Kniest Dysplasia, Achondroplasia, and Salpingo-Oophorectomy.
Their clinical research consists of co-authoring 55 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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.
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
- Thanatophoric DysplasiaSawai isDistinguished. Learn about Thanatophoric Dysplasia.
- Advanced
- Acanthosis NigricansSawai isAdvanced. Learn about Acanthosis Nigricans.
- AchondroplasiaSawai isAdvanced. Learn about Achondroplasia.
- Acromicric DysplasiaSawai isAdvanced. Learn about Acromicric Dysplasia.
- Hypophosphatasia (HPP)Sawai isAdvanced. Learn about Hypophosphatasia (HPP).
- Kniest DysplasiaSawai isAdvanced. Learn about Kniest Dysplasia.
- Trisomy 18Sawai isAdvanced. Learn about Trisomy 18.
- Experienced
- Alpha ThalassemiaSawai isExperienced. Learn about Alpha Thalassemia.
- Bannayan-Riley-Ruvalcaba Syndrome
- Brachydactyly Mononen TypeSawai isExperienced. Learn about Brachydactyly Mononen Type.
- Chromosome 13q DuplicationSawai isExperienced. Learn about Chromosome 13q Duplication.
- Cowden SyndromeSawai isExperienced. Learn about Cowden Syndrome.
- Down SyndromeSawai isExperienced. Learn about Down Syndrome.