Overview
Pavel Pichurin is a Medical Genetics specialist and a Pediatrics provider in Rochester, Minnesota. Dr. Pichurin and is rated as an Experienced provider by MediFind in the treatment of Nevoid Basal Cell Carcinoma Syndrome. His top areas of expertise are Cerebellar Hypoplasia, Cowden Syndrome, Peutz-Jeghers Syndrome, and Phacomatosis Pigmentovascularis.
His clinical research consists of co-authoring 48 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Sanford Health
- Cigna
- Medica
- Humana
- Florida Blue
Locations
Rochester, MN 55902
200 1st St Sw, Rochester, MN 55905
Additional Areas of Focus
Dr. Pichurin has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Cerebellar Hypoplasia
- Cowden Syndrome
- Hypothalamic Hamartomas
- Peutz-Jeghers Syndrome
- Phacomatosis Pigmentovascularis
- Advanced
- Coloboma
- Crouzon Syndrome
- Miller-Dieker Syndrome
- Oral-Facial-Digital Syndrome
- Smith-Magenis Syndrome
- Woodhouse-Sakati Syndrome
- Experienced
- 2q37 Deletion Syndrome
- 47 XYY Syndrome
- Aase Syndrome
- Abruzzo-Erickson Syndrome
- Achalasia Microcephaly Syndrome
- Acrodermatitis Enteropathica