Overview
Katerina Slaba practices practicing medicine in Brno, Czech Republic.
Her clinical expertise encompasses Adenylosuccinate Lyase Deficiency, PMM2-Congenital Disorder of Glycosylation, Fetal Edema, and Hydrops Fetalis.
She is actively involved in clinical research, co-authoring 20 peer reviewed articles.
Gender
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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 Katerina Slaba
Is Katerina Slaba a top-rated expert for Adenylosuccinate Lyase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Katerina Slaba is classified as an Experienced expert for Adenylosuccinate Lyase 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 Katerina Slaba participate in research or clinical trials?
Yes. Katerina Slaba has published 20 articles and abstracts on conditions like Adenylosuccinate Lyase Deficiency. You can view a list of Katerina Slaba'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
- Adenylosuccinate Lyase DeficiencyMs. Slaba isExperienced. Learn about Adenylosuccinate Lyase Deficiency.
- Alpha ThalassemiaMs. Slaba isExperienced. Learn about Alpha Thalassemia.
- Colorectal CancerMs. Slaba isExperienced. Learn about Colorectal Cancer.
- Fetal EdemaMs. Slaba isExperienced. Learn about Fetal Edema.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hemolytic Disease of the NewbornMs. Slaba isExperienced. Learn about Hemolytic Disease of the Newborn.
- Hydrops FetalisMs. Slaba isExperienced. Learn about Hydrops Fetalis.
- HypotoniaMs. Slaba isExperienced. Learn about Hypotonia.
- Intraventricular Hemorrhage of the Newborn
- Magnesium DeficiencyMs. Slaba isExperienced. Learn about Magnesium Deficiency.
- MosaicismMs. Slaba isExperienced. Learn about Mosaicism.
- NephrocalcinosisMs. Slaba isExperienced. Learn about Nephrocalcinosis.
- PMM2-Congenital Disorder of Glycosylation
- PolyhydramniosMs. Slaba isExperienced. Learn about Polyhydramnios.
- SeizuresMs. Slaba isExperienced. Learn about Seizures.
- Spastic Paraplegia Type 2Ms. Slaba isExperienced. Learn about Spastic Paraplegia Type 2.
- ThalassemiaMs. Slaba isExperienced. Learn about Thalassemia.