Overview
Hiroshi Mochizuki practices in Saitama, Japan. Mr. Mochizuki is rated as an Experienced expert by MediFind in the treatment of Urea Cycle Disorders (UCD). His top areas of expertise are Achondroplasia, Acanthosis Nigricans, Hypophosphatasia (HPP), and Argininosuccinic Aciduria.
His clinical research consists of co-authoring 15 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Urea Cycle Disorders (UCD).
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.
1 Clinical Trials
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
- Elite
- AchondroplasiaMr. Mochizuki isElite. Learn about Achondroplasia.
- Advanced
- Acanthosis NigricansMr. Mochizuki isAdvanced. Learn about Acanthosis Nigricans.
- Experienced
- Albright's Hereditary OsteodystrophyMr. Mochizuki isExperienced. Learn about Albright's Hereditary Osteodystrophy.
- Allan-Herndon-Dudley SyndromeMr. Mochizuki isExperienced. Learn about Allan-Herndon-Dudley Syndrome.
- Argininosuccinic AciduriaMr. Mochizuki isExperienced. Learn about Argininosuccinic Aciduria.
- Classic GalactosemiaMr. Mochizuki isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMr. Mochizuki isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Mochizuki isExperienced. Learn about Galactose Epimerase Deficiency.