Overview
Gittan Kollberg practices practicing medicine in Goeteborg, Sweden.
Kollberg is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Cytochrome C Oxidase Deficiency, Glycogen Storage Disease Type 0, MELAS Syndrome, and Retinopathy Pigmentary Mental Retardation.
They are actively involved in clinical research, co-authoring 21 peer reviewed articles.
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 Gittan Kollberg
Is Gittan Kollberg a top-rated expert for Cytochrome C Oxidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Gittan Kollberg is classified as an Distinguished expert for Cytochrome C Oxidase 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 Gittan Kollberg participate in research or clinical trials?
Yes. Gittan Kollberg has published 21 articles and abstracts on conditions like Cytochrome C Oxidase Deficiency. You can view a list of Gittan Kollberg'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
- Cytochrome C Oxidase DeficiencyKollberg isDistinguished. Learn about Cytochrome C Oxidase Deficiency.
- Advanced
- Glycogen Storage Disease Type 0
- Experienced
- CACH SyndromeKollberg isExperienced. Learn about CACH Syndrome.
- DysarthriaKollberg isExperienced. Learn about Dysarthria.
- Kearns-Sayre SyndromeKollberg isExperienced. Learn about Kearns-Sayre Syndrome.
- MELAS SyndromeKollberg isExperienced. Learn about MELAS Syndrome.
- Progressive External Ophthalmoplegia
- Pyruvate Decarboxylase DeficiencyKollberg isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyKollberg isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Retinopathy Pigmentary Mental Retardation
- RhabdomyolysisKollberg isExperienced. Learn about Rhabdomyolysis.
- Sialic Acid Storage DiseaseKollberg isExperienced. Learn about Sialic Acid Storage Disease.
- SialuriaKollberg isExperienced. Learn about Sialuria.