Overview
Radhika Dhamija is a Medical Genetics specialist and a Neurologist in Rochester, Minnesota. Dr. Dhamija and is rated as an Experienced provider by MediFind in the treatment of Congenital Toxoplasmosis. Her top areas of expertise are Retinal Vasculopathy with Cerebral Leukodystrophy, Cowden Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, and Lhermitte-Duclos Disease.
Her clinical research consists of co-authoring 78 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Congenital Toxoplasmosis.
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
Locations
200 1st St Sw, Rochester, MN 55905
Additional Areas of Focus
Dr. Dhamija 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.
1 Clinical Trials
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
- Bannayan-Riley-Ruvalcaba Syndrome
- Cowden Syndrome
- Lhermitte-Duclos Disease
- Retinal Vasculopathy with Cerebral Leukodystrophy
- Advanced
- Ehlers-Danlos Syndrome (EDS)
- Myoclonic Epilepsy
- Neurofibromatosis
- Neurofibromatosis Type 1 (NF1)
- Ruvalcaba Syndrome
- Split Hand Foot Malformation
- Experienced
- Absence Seizure
- Achalasia Microcephaly Syndrome
- Acute Cerebellar Ataxia
- Aplasia Cutis Congenita
- Arteriovenous Malformation
- Benign Familial Neonatal Seizures