Overview
Karolina Peskova practices practicing medicine in Prague, Czech Republic.
Ms. Peskova is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Carnitine-Acylcarnitine Translocase Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Glycogen Storage Disease Type 9, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
She is actively involved in clinical research, co-authoring 10 peer reviewed articles.
Gender
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.
Frequently Asked Questions about Karolina Peskova
Is Karolina Peskova a top-rated expert for Carnitine-Acylcarnitine Translocase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Karolina Peskova is classified as an Advanced expert for Carnitine-Acylcarnitine Translocase Deficiency, 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 Karolina Peskova participate in research or clinical trials?
Yes. Karolina Peskova has published 10 articles and abstracts on conditions like Carnitine-Acylcarnitine Translocase Deficiency. You can view a list of Karolina Peskova'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
- Advanced
- Carnitine-Acylcarnitine Translocase Deficiency
- Experienced
- Carnitine Palmitoyltransferase 1 Deficiency
- Enlarged LiverMs. Peskova isExperienced. Learn about Enlarged Liver.
- Familial HypertriglyceridemiaMs. Peskova isExperienced. Learn about Familial Hypertriglyceridemia.
- Glycogen Storage Disease Type 9Ms. Peskova isExperienced. Learn about Glycogen Storage Disease Type 9.
- Homocystinuria due to MTHFR DeficiencyMs. Peskova isExperienced. Learn about Homocystinuria due to MTHFR Deficiency.
- Mucopolysaccharidoses (MPS)Ms. Peskova isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- X-Linked AgammaglobulinemiaMs. Peskova isExperienced. Learn about X-Linked Agammaglobulinemia.