Dr. Jessica R. Priestley
Overview
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Experienced provider by MediFind in the treatment of Leigh Syndrome. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Leigh Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- 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
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
35 Michigan Street Northeast, Suite 3003, Grand Rapids, MI 49503
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
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.
Robert Conway is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Conway is rated as an Advanced provider by MediFind in the treatment of Leigh Syndrome. 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.
Gregory Trowbridge is a Pediatrics provider in Grand Rapids, Michigan. Dr. Trowbridge is rated as an Experienced provider by MediFind in the treatment of Leigh Syndrome. His top areas of expertise are Malnutrition, Maternally Inherited Leigh Syndrome, Leigh Syndrome, Respiratory Syncytial Virus (RSV) Infection, and Myringotomy.
Edward W Sparrow Hospital Association
Erika Erlandson is a Physiatrist and a Pediatrics provider in Lansing, Michigan. Dr. Erlandson is rated as an Experienced provider by MediFind in the treatment of Leigh Syndrome. Her top areas of expertise are Cerebral Palsy, Spastic Diplegia Infantile Type, Spasticity, and Foot Drop. Dr. Erlandson 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
- Autosomal Recessive Congenital Methemoglobinemia
- Biotinidase DeficiencyDr. Priestley isAdvanced. Learn about Biotinidase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Classic GalactosemiaDr. Priestley isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Priestley isAdvanced. Learn about Danon Disease.
- Experienced
- 15q11.2 MicrodeletionDr. Priestley isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Priestley isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Priestley isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Priestley isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Priestley isExperienced. Learn about 47 XYY Syndrome.