Overview
Stacie Adams is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Adams is rated as an Experienced provider by MediFind in the treatment of Activated PI3K Delta Syndrome (APDS). Her top areas of expertise are Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactosemia. Dr. Adams is currently accepting new patients.
Her clinical research consists of co-authoring 7 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
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- 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
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- 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
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.
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 8 years and is rated as an Advanced provider by MediFind in the treatment of Activated PI3K Delta Syndrome (APDS). Her top areas of expertise are Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.
Alger Pediatrics
Ronald Hofman is a Pediatrics provider in Grand Rapids, Michigan. Dr. Hofman has been practicing medicine for over 45 years and is rated as an Advanced provider by MediFind in the treatment of Activated PI3K Delta Syndrome (APDS). His top areas of expertise are Obesity in Children, Roseola, Croup, and Oppositional Defiant Disorder (ODD). Dr. Hofman is currently accepting new patients.
Corewell Health Pediatric Hospitalists - Grand Rapids
Nicholas Beam is a Pediatrics provider in Grand Rapids, Michigan. Dr. Beam has been practicing medicine for over 8 years and is rated as an Experienced provider by MediFind in the treatment of Activated PI3K Delta Syndrome (APDS). His top areas of expertise are Malnutrition, Respiratory Syncytial Virus (RSV) Infection, Genetic Epilepsy with Febrile Seizures Plus (GEFS+), and Streptococcal Group A Infection.
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
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Argininosuccinic AciduriaDr. Adams isAdvanced. Learn about Argininosuccinic Aciduria.
- Biotinidase DeficiencyDr. Adams isAdvanced. Learn about Biotinidase Deficiency.
- Classic GalactosemiaDr. Adams isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Adams isAdvanced. Learn about Danon Disease.
- Dihydropteridine Reductase Deficiency
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Adams isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adrenoleukodystrophy (ALD)Dr. Adams isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Adams isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency