Overview
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Classic Galactosemia. Dr. Ahmad is currently accepting new patients.
Her clinical research consists of co-authoring 37 peer reviewed articles and participating in 2 clinical trials. 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
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- PPO
- 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
1500 E Medical Ctr Dr, Ann Arbor, MI 48109
1500 E Medical Ctr, Suite 0331, Ann Arbor, MI 48109
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
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 Hyperlysinemia. Her top areas of expertise are Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome.
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 Hyperlysinemia. His top areas of expertise are Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Propionic Acidemia.
Regents Of The University Of Michigan
Elizabeth Ames is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ames is rated as an Advanced provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Delayed Growth, Cardiomyopathic Lentiginosis, Noonan Syndrome, and Cardiofaciocutaneous Syndrome. Dr. Ames 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
- Elite
- Pompe DiseaseDr. Ahmad isElite. Learn about Pompe Disease.
- Distinguished
- Classic GalactosemiaDr. Ahmad isDistinguished. Learn about Classic Galactosemia.
- Inborn Amino Acid Metabolism DisorderDr. Ahmad isDistinguished. Learn about Inborn Amino Acid Metabolism Disorder.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Propionic AcidemiaDr. Ahmad isDistinguished. Learn about Propionic Acidemia.
- Von Gierke DiseaseDr. Ahmad isDistinguished. Learn about Von Gierke Disease.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Andersen DiseaseDr. Ahmad isAdvanced. Learn about Andersen Disease.
- Argininosuccinic AciduriaDr. Ahmad isAdvanced. Learn about Argininosuccinic Aciduria.
- Beta-Ketothiolase DeficiencyDr. Ahmad isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency
- Experienced
- 15q11.2 MicrodeletionDr. Ahmad isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Ahmad isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Ahmad isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Ahmad isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Ahmad isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Ahmad isExperienced. Learn about Aase Syndrome.