Overview
Dorina Supak practices practicing medicine in Budapest, Hungary.
Her clinical expertise encompasses Chromosome 13q Duplication, Trisomy 13, Preeclampsia, and Trisomy 18.
She is actively involved in clinical research, co-authoring 10 peer reviewed articles.
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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 Dorina Supak
Is Dorina Supak a top-rated expert for Chromosome 13q Duplication?
MediFind is an objective health platform that identifies experts based on real-world data. Dorina Supak is classified as an Experienced expert for Chromosome 13q Duplication, 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 Dorina Supak participate in research or clinical trials?
Yes. Dorina Supak has published 10 articles and abstracts on conditions like Chromosome 13q Duplication. You can view a list of Dorina Supak'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
- Experienced
- Chromosome 13q DuplicationMs. Supak isExperienced. Learn about Chromosome 13q Duplication.
- PreeclampsiaMs. Supak isExperienced. Learn about Preeclampsia.
- Trisomy 13Ms. Supak isExperienced. Learn about Trisomy 13.
- Trisomy 18Ms. Supak isExperienced. Learn about Trisomy 18.