Overview
Stefan Vlaho practices practicing medicine in Altoetting, Germany.
His clinical expertise encompasses PEPCK 1 Deficiency, Klippel-Feil Syndrome, Frontonasal Dysplasia Klippel Feil Syndrome, and Hypotonia.
He is actively involved in clinical research, co-authoring 8 peer reviewed articles.
Gender
Locations
Altoetting, BY, 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 Stefan Vlaho
Is Stefan Vlaho a top-rated expert for PEPCK 1 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Stefan Vlaho is classified as an Experienced expert for PEPCK 1 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 Stefan Vlaho participate in research or clinical trials?
Yes. Stefan Vlaho has published 8 articles and abstracts on conditions like PEPCK 1 Deficiency. You can view a list of Stefan Vlaho'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
- Frontonasal Dysplasia Klippel Feil Syndrome
- HypotoniaMr. Vlaho isExperienced. Learn about Hypotonia.
- Klippel-Feil SyndromeMr. Vlaho isExperienced. Learn about Klippel-Feil Syndrome.
- PEPCK 1 DeficiencyMr. Vlaho isExperienced. Learn about PEPCK 1 Deficiency.