Overview
Robert Conway is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Conway is rated as an Experienced provider by MediFind in the treatment of Classic Galactosemia. His top areas of expertise are Hypermethioninemia, Biotinidase Deficiency, Phenylketonuria (PKU), and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Conway is currently accepting new patients.
His clinical research consists of co-authoring 21 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Classic Galactosemia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MEDICARE MAPD
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.
2 Clinical Trials
Stacie Adams is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of Classic Galactosemia. Her top areas of expertise are Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactosemia. Dr. Adams is currently accepting new patients.
Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 7 years and is rated as an Advanced provider by MediFind in the treatment of Classic Galactosemia. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.
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
- Distinguished
- Biotinidase DeficiencyDr. Conway isDistinguished. Learn about Biotinidase Deficiency.
- HypermethioninemiaDr. Conway isDistinguished. Learn about Hypermethioninemia.
- Advanced
- Dihydropteridine Reductase Deficiency
- Isovaleric AcidemiaDr. Conway isAdvanced. Learn about Isovaleric Acidemia.
- Maternal HyperphenylalaninemiaDr. Conway isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Dr. Conway isAdvanced. Learn about Phenylketonuria (PKU).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Conway isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- CitrullinemiaDr. Conway isExperienced. Learn about Citrullinemia.
- Classic GalactosemiaDr. Conway isExperienced. Learn about Classic Galactosemia.
- Cortical DysplasiaDr. Conway isExperienced. Learn about Cortical Dysplasia.
- Danon DiseaseDr. Conway isExperienced. Learn about Danon Disease.
- Gastroesophageal Reflux in InfantsDr. Conway isExperienced. Learn about Gastroesophageal Reflux in Infants.