Overview
Tarachandra Narumanchi is a Medical Genetics specialist and a Pediatrics provider in Oklahoma City, Oklahoma. Dr. Narumanchi is highly rated in 8 conditions, according to our data. Their top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Tyrosinemia Type 1.
Their clinical research consists of co-authoring 3 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance plans
- Cigna
- Blue Cross Blue Shield
- Anthem
- CareSource
- Humana
Locations
1200 Childrens Ave, Oklahoma City, OK 73104
Additional Areas of Focus
Dr. Narumanchi 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
John Mulvihill is a Medical Genetics provider in Oklahoma City, Oklahoma. Dr. Mulvihill is highly rated in 3 conditions, according to our data. His top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Split Hand Foot Malformation, and Clouston Syndrome.
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Matthew Payne is a Pediatrics specialist and an Internal Medicine provider in Stillwater, Oklahoma. Dr. Payne is highly rated in 16 conditions, according to our data. His top areas of expertise are Sepsis, Encephalitis, Hypertensive Heart Disease, Gastrostomy, and Hip Replacement. Dr. Payne is currently accepting new 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.
- Advanced
- Chromosome 10q Deletion
- Citrullinemia
- Dihydropteridine Reductase Deficiency
- Maternal Hyperphenylalaninemia
- Phenylketonuria (PKU)
- Tyrosinemia Type 1
- Experienced
- Brittle Cornea Syndrome
- Dandy-Walker Syndrome
- Ehlers-Danlos Syndrome (EDS)
- Gerstmann-Straussler-Scheinker Syndrome
- Glutaric Acidemia Type 1
- Hyperlysinemia