Overview
Judit Balog practices practicing medicine in Leiden, Netherlands.
Ms. Balog is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Facioscapulohumeral Muscular Dystrophy (FSHD), Chromosome 18p Deletion, and RUNX1 Familial Platelet Disorder.
She is actively involved in clinical research, co-authoring 34 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 Judit Balog
Is Judit Balog a top-rated expert for Facioscapulohumeral Muscular Dystrophy (FSHD)?
MediFind is an objective health platform that identifies experts based on real-world data. Judit Balog is classified as an Distinguished expert for Facioscapulohumeral Muscular Dystrophy (FSHD), 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 Judit Balog participate in research or clinical trials?
Yes. Judit Balog has published 34 articles and abstracts on conditions like Facioscapulohumeral Muscular Dystrophy (FSHD). You can view a list of Judit Balog'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
- Distinguished
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Advanced
- Chromosome 18p DeletionMs. Balog isAdvanced. Learn about Chromosome 18p Deletion.
- Experienced
- RUNX1 Familial Platelet DisorderMs. Balog isExperienced. Learn about RUNX1 Familial Platelet Disorder.