Overview
Ivan Sebesta practices in Prague, Czech Republic. Mr. Sebesta is rated as an Elite expert by MediFind in the treatment of Hereditary Xanthinuria. His top areas of expertise are Hereditary Xanthinuria, Molybdenum Cofactor Deficiency (MoCD), Fanconi Syndrome, and Fanconi Bickel Syndrome.
His clinical research consists of co-authoring 16 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 6 articles in the study of Hereditary Xanthinuria.
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
- Elite
- Hereditary XanthinuriaMr. Sebesta isElite. Learn about Hereditary Xanthinuria.
- Experienced
- CystinosisMr. Sebesta isExperienced. Learn about Cystinosis.
- Fanconi Bickel SyndromeMr. Sebesta isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMr. Sebesta isExperienced. Learn about Fanconi Syndrome.
- GoutMr. Sebesta isExperienced. Learn about Gout.
- Molybdenum Cofactor Deficiency (MoCD)Mr. Sebesta isExperienced. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)