Expertise in
1
conditions

Ivan Sebesta

Prague, PR, CZ 
Expertise in
1
conditions
Prague, PR, CZ 

Overview

Ivan Sebesta practices practicing medicine in Prague, Czech Republic.

Mr. Sebesta is highly rated in 1 condition, according to our data. His clinical expertise encompasses Hereditary Xanthinuria, Molybdenum Cofactor Deficiency (MoCD), Fanconi Syndrome, and Fanconi Bickel Syndrome.

He is actively involved in clinical research, co-authoring 14 peer reviewed articles.

Gender

Male

Locations

Prague, PR, Czech Republic

Frequently Asked Questions about Ivan Sebesta

Is Ivan Sebesta a top-rated expert for Hereditary Xanthinuria?

MediFind is an objective health platform that identifies experts based on real-world data. Ivan Sebesta is classified as an Elite expert for Hereditary Xanthinuria, 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.

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

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