Overview
Courtney Strohacker is a Pediatric Cardiologist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Strohacker is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Hypoplastic Left Heart Syndrome (HLHS), Mitral Atresia, Tetralogy of Fallot, Ventricular Septal Defects, and Patent Foramen Ovale Repair. Dr. Strohacker is currently accepting new patients.
Her clinical research consists of co-authoring 12 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
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- 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.
Regents Of The University Of Michigan
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Quinonez is rated as a Distinguished provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Propionic Acidemia.
Regents Of The University Of Michigan
Kristen Lee is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome.
Regents Of The University Of Michigan
Amanda Pritchard is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Pritchard is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Aase Syndrome.
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
- Coarctation of the AortaDr. Strohacker isAdvanced. Learn about Coarctation of the Aorta.
- Congenital Heart Disease (CHD)Dr. Strohacker isAdvanced. Learn about Congenital Heart Disease (CHD).
- DiGeorge SyndromeDr. Strohacker isAdvanced. Learn about DiGeorge Syndrome.
- Double Aortic ArchDr. Strohacker isAdvanced. Learn about Double Aortic Arch.
- Double Outlet Right VentricleDr. Strohacker isAdvanced. Learn about Double Outlet Right Ventricle.
- Heart MurmursDr. Strohacker isAdvanced. Learn about Heart Murmurs.
- Experienced
- 15q11.2 MicrodeletionDr. Strohacker isExperienced. Learn about 15q11.2 Microdeletion.
- Aberrant Subclavian ArteryDr. Strohacker isExperienced. Learn about Aberrant Subclavian Artery.
- Anomalous Left Coronary Artery from the Pulmonary Artery
- Aortic RegurgitationDr. Strohacker isExperienced. Learn about Aortic Regurgitation.
- Atrial Septal Defect (ASD)Dr. Strohacker isExperienced. Learn about Atrial Septal Defect (ASD).
- Atrioventricular Septal DefectDr. Strohacker isExperienced. Learn about Atrioventricular Septal Defect.