Overview
My practice includes caring for children and adults with inherited conditions, such as inherited disorders of metabolism, genetic syndromes, mitochondrial disorders, inherited causes of growth failure or developmental delay, and conditions detected by newborn screening. My clinic works with the Pediatric Biochemical Genetics Laboratory to diagnose these conditions. We provide treatment for inherited disorders of metabolism. I work closely with the geneticists, neurologists, pediatricians, internists, and other providers at Duke University Medical Center to provide comprehensive care for my patients. My research has been aimed at developing new treatments for inherited conditions, focusing on glycogen storage diseases, like Pompe disease and von Gierke disease. We have developed gene therapy for these conditions and are in the process of starting clinical trials to test safety and benefits.
Dr. Koeberl is highly rated in 16 conditions, according to our data. His clinical expertise encompasses Pompe Disease, Von Gierke Disease, Propionic Acidemia, and X-Linked Creatine Deficiency.
Dr. Koeberl is board certified in American Board Of Medical Genetics, Clinical Biochemical Genetics , American Board Of Medical Genetics, Clinical Genetics And Genomics - General , and American Board Of Pediatrics, General Pediatrics. He is actively involved in clinical research, co-authoring 107 peer reviewed articles and participating in 2 clinical trials. Dr. Koeberl is currently accepting new patients.
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- POS
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
2301 Erwin Rd, Durham, NC 27710
3000 Erwin Rd, Durham, NC 27705
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.
2 Clinical Trials
Lenox Baker Children's Hospital
I am a clinical geneticist and a pediatrician with a deep interest in undiagnosed and rare genetic disorders. I provide medical care for children and adults with chromosome 22q11.2 deletion syndrome and diagnostic evaluation for patients with symptoms and signs of genetic disorders, when evaluations have not provided a specific diagnosis. Dr. Shashi is highly rated in 8 conditions, according to our data. Her clinical expertise encompasses DiGeorge Syndrome, Hypotonia, Immune Defect due to Absence of Thymus, and Micrognathia. Dr. Shashi is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics - General. Dr. Shashi is currently accepting new patients.
Duke Health Integrated Practice Inc
Priya Kishnani is a Pediatrics provider practicing medicine in Durham, North Carolina. Dr. Kishnani is highly rated in 10 conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Glycogen Storage Disease Type 3, Hypophosphatasia (HPP), Glycogen Storage Disease Type 9, and Splenectomy. Dr. Kishnani is currently accepting new patients.
Duke Cancer Center Brain Tumor Clinic
I am an academic adult and pediatric neuro-oncologist who helps lead The Preston Robert Tisch Brain Tumor Center at Duke. I am the author of more than 500 peer-reviewed articles, reviews, and book chapters, and I have presented extensively at both international and national meetings. I am a committed educator who is a member of the executive and super-executive committees of the Duke University School of Medicine, which are responsible for the recruitment, screening and selection of medical students. I have reviewed grants for the National Institutes of Health for over 15 years, in a spectrum of different study sections. I am the senior editor of CNS Oncology and a reviewer for over 25 academic journals. I serve on the advisory board of a number of organizations, including Voices Against Brain Cancer, the Tug McGraw Foundation, Pinnacle Care, the Pediatric Brain Tumor Foundation, the National Children’s Cancer Society, and the American Brain Tumor Association. Dr. Friedman is highly rated in 18 conditions, according to our data. His clinical expertise encompasses Glioma, Astrocytoma, Glioblastoma, and Brain Tumor. Dr. Friedman is board certified in American Board Of Pediatrics, General Pediatrics and American Board Of Pediatrics, Pediatric Hematology-Oncology. Dr. Friedman is currently accepting new patients.
Frequently Asked Questions about Dr. Dwight D. Koeberl
How do I make an appointment with Dr. Dwight D. Koeberl?
You can book an appointment with Dr. Dwight D. Koeberl by calling their office at 919-684-8111. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Dwight D. Koeberl a top-rated expert for Pompe Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Dwight D. Koeberl is classified as an Elite expert for Pompe Disease, 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. Dwight D. Koeberl specialize in?
While Dr. Dwight D. Koeberl is a Medical Genetics, they have specific expertise in Pompe Disease, Von Gierke Disease, and Propionic Acidemia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Dwight D. Koeberl participate in research or clinical trials?
Yes. Dr. Dwight D. Koeberl has published 107 articles and abstracts on conditions like Pompe Disease. You can view a list of Dr. Dwight D. Koeberl's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Dwight D. Koeberl accept my insurance?
Dr. Dwight D. Koeberl accepts most major insurance plans, including Aetna and Ambetter. We recommend calling the office directly at 919-684-8111 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
- Elite
- Pompe DiseaseDr. Koeberl isElite. Learn about Pompe Disease.
- Distinguished
- Propionic AcidemiaDr. Koeberl isDistinguished. Learn about Propionic Acidemia.
- Von Gierke DiseaseDr. Koeberl isDistinguished. Learn about Von Gierke Disease.
- X-Linked Creatine DeficiencyDr. Koeberl isDistinguished. Learn about X-Linked Creatine Deficiency.
- Advanced
- CitrullinemiaDr. Koeberl isAdvanced. Learn about Citrullinemia.
- Classic GalactosemiaDr. Koeberl isAdvanced. Learn about Classic Galactosemia.
- Coenzyme Q Cytochrome C Reductase Deficiency
- Galactose Epimerase DeficiencyDr. Koeberl isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Koeberl isAdvanced. Learn about Galactosemia.
- Glycogen Storage Disease Type 0Dr. Koeberl isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Kearns-Sayre SyndromeDr. Koeberl isAdvanced. Learn about Kearns-Sayre Syndrome.
- MELAS SyndromeDr. Koeberl isAdvanced. Learn about MELAS Syndrome.
- Mitochondrial Complex 1 DeficiencyDr. Koeberl isAdvanced. Learn about Mitochondrial Complex 1 Deficiency.
- Mitochondrial Trifunctional Protein Deficiency
- Pyruvate Carboxylase DeficiencyDr. Koeberl isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Thymidine Kinase 2 Deficiency (TK2d)
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Alternating Hemiplegia of ChildhoodDr. Koeberl isExperienced. Learn about Alternating Hemiplegia of Childhood.
- Autism Spectrum DisorderDr. Koeberl isExperienced. Learn about Autism Spectrum Disorder.
- HypotoniaDr. Koeberl isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Koeberl isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Koeberl isExperienced. Learn about Maple Syrup Urine Disease.
- Newborn JaundiceDr. Koeberl isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarDr. Koeberl isExperienced. Learn about Newborn Low Blood Sugar.
- Progressive External OphthalmoplegiaDr. Koeberl isExperienced. Learn about Progressive External Ophthalmoplegia.
- Spasmus NutansDr. Koeberl isExperienced. Learn about Spasmus Nutans.
- Urea Cycle Disorders (UCD)Dr. Koeberl isExperienced. Learn about Urea Cycle Disorders (UCD).