Overview
Mari Mori is a Medical Genetics specialist and a Pediatrics provider in Atlanta, Georgia. Dr. Mori is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Glycogen Storage Disease Type 7, FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Von Gierke Disease. Dr. Mori is currently accepting new patients.
Her clinical research consists of co-authoring 33 peer reviewed articles. 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
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- HMO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
Locations
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.
Emory Clinic At 1365 Clifton Road
Hong Li is a Medical Genetics provider in Atlanta, Georgia. Dr. Li has been practicing medicine for over 32 years and is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Beta-Ketothiolase Deficiency.
Emory Clinic At 1365 Clifton Road
William Wilcox is a Medical Genetics provider in Atlanta, Georgia. Dr. Wilcox has been practicing medicine for over 38 years and is rated as a Distinguished provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
Juanita Neira-Fresneda is a Medical Genetics specialist and a Pediatrics provider in Atlanta, Georgia. Dr. Neira-Fresneda is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Potocki-Lupski Syndrome, Smith-Magenis Syndrome, Trisomy 17 Mosaicism, and Phenylketonuria (PKU). Dr. Neira-Fresneda 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
- Andersen DiseaseDr. Mori isAdvanced. Learn about Andersen Disease.
- Danon DiseaseDr. Mori isAdvanced. Learn about Danon Disease.
- FG SyndromeDr. Mori isAdvanced. Learn about FG Syndrome.
- Glycogen Storage Disease Type 7
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Ornithine Transcarbamylase Deficiency
- Experienced
- 3MC SyndromeDr. Mori isExperienced. Learn about 3MC Syndrome.
- Acromicric DysplasiaDr. Mori isExperienced. Learn about Acromicric Dysplasia.
- Alpha ThalassemiaDr. Mori isExperienced. Learn about Alpha Thalassemia.
- Arginase DeficiencyDr. Mori isExperienced. Learn about Arginase Deficiency.
- Atypical Hemolytic Uremic Syndrome (aHUS)
- Beta-Ketothiolase DeficiencyDr. Mori isExperienced. Learn about Beta-Ketothiolase Deficiency.