Overview
Priya Kishnani is a Pediatrics provider in Durham, North Carolina. Dr. Kishnani and is rated as an Elite provider by MediFind in the treatment of Glycogen Storage Disease Type 9. Her top areas of expertise are Pompe Disease, Glycogen Storage Disease Type 3, Hypophosphatasia (HPP), Glycogen Storage Disease Type 9, and Splenectomy. Dr. Kishnani is currently accepting new patients.
Her clinical research consists of co-authoring 319 peer reviewed articles and participating in 11 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 6 articles in the study of Glycogen Storage Disease Type 9.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Cigna
- Blue Cross Blue Shield
- Humana
- Piedmont
Locations
40 Duke Medicine Cir, Durham, NC 27710
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.
11 Clinical Trials
The Moses H Cone Memorial Hospital Operating Corporation
Chad Haldeman is a Medical Genetics specialist and a Pediatrics provider in Greensboro, North Carolina. Dr. Haldeman and is rated as an Advanced provider by MediFind in the treatment of Glycogen Storage Disease Type 9. His top areas of expertise are Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Mucopolysaccharidoses (MPS).
Duke Health Integrated Practice Inc
Areeg El-Gharbawy is a Medical Genetics specialist and an Endocrinologist in Durham, North Carolina. Dr. El-Gharbawy and is rated as an Advanced provider by MediFind in the treatment of Glycogen Storage Disease Type 9. Her top areas of expertise are Von Gierke Disease, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Mitochondrial Trifunctional Protein Deficiency, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. El-Gharbawy 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.
- Elite
- Gaucher Disease
- Gaucher Disease Type 1
- Glycogen Storage Disease Type 3
- Glycogen Storage Disease Type 9
- Hypophosphatasia (HPP)
- Pompe Disease
- Distinguished
- Gaucher Disease Type 3
- Experienced
- Anemia
- Childhood Iron Deficiency Anemia
- Delayed Growth
- Glycogen Storage Disease Type 7
- Hypotonia
- Increased Head Circumference