Overview
Dimitar Gavrilov is a Pediatrics provider practicing medicine in Rochester, Minnesota.
Dr. Gavrilov is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Malonyl-CoA Decarboxylase Deficiency, Zellweger Syndrome, Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Pompe Disease.
He is actively involved in clinical research, co-authoring 42 peer reviewed articles. Dr. Gavrilov is currently accepting new patients.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- PPO
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. Providers 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.
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Frequently Asked Questions about Dr. Dimitar K. Gavrilov
How do I make an appointment with Dr. Dimitar K. Gavrilov?
You can book an appointment with Dr. Dimitar K. Gavrilov by calling their office at 507-284-2511. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Dimitar K. Gavrilov a top-rated expert for Malonyl-CoA Decarboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Dimitar K. Gavrilov is classified as an Advanced expert for Malonyl-CoA Decarboxylase 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.
What conditions does Dr. Dimitar K. Gavrilov specialize in?
While Dr. Dimitar K. Gavrilov is a Pediatrics, they have specific expertise in Malonyl-CoA Decarboxylase Deficiency, Zellweger Syndrome, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Dimitar K. Gavrilov participate in research or clinical trials?
Yes. Dr. Dimitar K. Gavrilov has published 42 articles and abstracts on conditions like Malonyl-CoA Decarboxylase Deficiency. You can view a list of Dr. Dimitar K. Gavrilov's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Dimitar K. Gavrilov accept my insurance?
Dr. Dimitar K. Gavrilov accepts most major insurance plans, including Medica. We recommend calling the office directly at 507-284-2511 to verify that your specific plan is currently accepted before your visit.
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
- Advanced
- Malonyl-CoA Decarboxylase DeficiencyDr. Gavrilov isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Zellweger SyndromeDr. Gavrilov isAdvanced. Learn about Zellweger Syndrome.
- Experienced
- Gaucher DiseaseDr. Gavrilov isExperienced. Learn about Gaucher Disease.
- Glutaric Acidemia Type 2Dr. Gavrilov isExperienced. Learn about Glutaric Acidemia Type 2.
- Mucopolysaccharidoses (MPS)Dr. Gavrilov isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Niemann-Pick DiseaseDr. Gavrilov isExperienced. Learn about Niemann-Pick Disease.
- Pompe DiseaseDr. Gavrilov isExperienced. Learn about Pompe Disease.
- Short-Chain Acyl-CoA Dehydrogenase Deficiency