Leipzig, SN, DE 

Overview

Urs Berger practices practicing medicine in Leipzig, Germany.

Their clinical expertise encompasses Chromosome 2 Uniparental Disomy, Carnitine Palmitoyltransferase 1 Deficiency, Pierre Robin Sequence, and Micrognathia.

They are actively involved in clinical research, co-authoring 56 peer reviewed articles.

Locations

Leipzig, SN 04318, Germany
Other Locations
Freiburg, BW, Germany
Jena, TH, Germany

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 Urs V. Berger

Is Urs V. Berger a top-rated expert for Chromosome 2 Uniparental Disomy?

MediFind is an objective health platform that identifies experts based on real-world data. Urs V. Berger is classified as an Experienced expert for Chromosome 2 Uniparental Disomy, 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 Urs V. Berger participate in research or clinical trials?

Yes. Urs V. Berger has published 56 articles and abstracts on conditions like Chromosome 2 Uniparental Disomy. You can view a list of Urs V. Berger'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.

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