Overview
Danielle Demarzo is a Medical Genetics specialist and an Obstetrics and Gynecologist in Oklahoma City, Oklahoma. Dr. Demarzo is rated as an Experienced provider by MediFind in the treatment of 15q11.2 Microdeletion. Her top areas of expertise are Micrognathia, Isovaleric Acidemia, Glycogen Storage Disease Type 3, and Hypotonia.
Her clinical research consists of co-authoring 6 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
Locations
1200 Childrens Ave, Suite B770, Oklahoma City, OK 73104
900 Ne 10th St, Ouhp Family Medicine, Oklahoma City, OK 73104
Additional Areas of Focus
Dr. Demarzo 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
Ou Health Partners Inc
Tarachandra Narumanchi is a Medical Genetics specialist and a Pediatrics provider in Oklahoma City, Oklahoma. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of 15q11.2 Microdeletion. His top areas of expertise are Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
Molly Khoury is a Pediatrics provider in Oklahoma City, Oklahoma. Dr. Khoury is rated as an Experienced provider by MediFind in the treatment of 15q11.2 Microdeletion. Her top areas of expertise are Microcephaly Deafness Syndrome, Early Infantile Epileptic Encephalopathy, CHARGE Syndrome, and Wildervanck Syndrome. Dr. Khoury is currently accepting new patients.
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
- Advanced
- MicrognathiaDr. Demarzo isAdvanced. Learn about Micrognathia.
- Experienced
- 15q11.2 MicrodeletionDr. Demarzo isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Demarzo isExperienced. Learn about 3p Deletion Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Demarzo isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Chromosome 12p DeletionDr. Demarzo isExperienced. Learn about Chromosome 12p Deletion.
- Chromosome 15q DeletionDr. Demarzo isExperienced. Learn about Chromosome 15q Deletion.