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 Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). 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.
Jennifer Curtis is a Pediatrics provider in Grand Rapids, Michigan. Dr. Curtis is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). Her top areas of expertise are Trisomy 13, Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). Dr. Curtis is currently accepting new patients.
Karl Nicles is a Pediatrics provider in Norton Shores, Michigan. Dr. Nicles is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). His top areas of expertise are Obesity in Children, Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), Croup, and Autism Spectrum Disorder. Dr. Nicles is currently accepting new patients.
Spectrum Health Primary Care Partners
Meghan Behrmann is a Developmental and Behavioral Pediatrics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Behrmann is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). Her top areas of expertise are Autism Spectrum Disorder, Delayed Growth, Cardiofaciocutaneous Syndrome, and Distal 18q Deletion Syndrome. Dr. Behrmann 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
- 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