Overview
Emily Shelkowitz is a Pediatrics provider in Aurora, Colorado. Dr. Shelkowitz is rated as an Experienced provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. Her top areas of expertise are Hyperlysinemia, Glycogen Storage Disease Type 3, Pompe Disease, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Shelkowitz is currently accepting new patients.
Her clinical research consists of co-authoring 13 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
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- HMO
- MANAGED MEDICAID PLAN
- HMO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- PPO
- EPO
- HMO
- POS
- PPO
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.
University Physicians Incorporated
Jason Weinman is a Pediatric Radiologist and a Radiologist in Aurora, Colorado. Dr. Weinman is rated as an Advanced provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. His top areas of expertise are Phosphoglycerate Mutase Deficiency, High Blood Pressure in Infants, Interstitial Lung Disease, and Cerebral Hypoxia.
University Physicians Incorporated
Csaba Galambos is a Pediatrics provider in Aurora, Colorado. Dr. Galambos is rated as a Distinguished provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. His top areas of expertise are High Blood Pressure in Infants, Phosphoglycerate Mutase Deficiency, Pulmonary Hypertension, Cerebral Hypoxia, and Tissue Biopsy. Dr. Galambos is currently accepting new patients.
University Physicians Incorporated
Robin Deterding is a Pediatric Pulmonologist and a Pediatrics provider in Aurora, Colorado. Dr. Deterding is rated as a Distinguished provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. Her top areas of expertise are Interstitial Lung Disease, Acute Interstitial Pneumonia, Phosphoglycerate Mutase Deficiency, Endoscopy, and Gastrostomy. Dr. Deterding 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
- Glycogen Storage Disease Type 3Dr. Shelkowitz isAdvanced. Learn about Glycogen Storage Disease Type 3.
- HyperlysinemiaDr. Shelkowitz isAdvanced. Learn about Hyperlysinemia.
- Experienced
- Glycogen Storage Disease Type 0Dr. Shelkowitz isExperienced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 13Dr. Shelkowitz isExperienced. Learn about Glycogen Storage Disease Type 13.
- Glycogen Storage Disease Type 7Dr. Shelkowitz isExperienced. Learn about Glycogen Storage Disease Type 7.
- Glycogen Storage Disease Type 9Dr. Shelkowitz isExperienced. Learn about Glycogen Storage Disease Type 9.
- Increased Head CircumferenceDr. Shelkowitz isExperienced. Learn about Increased Head Circumference.
- Mitochondrial Trifunctional Protein DeficiencyDr. Shelkowitz isExperienced. Learn about Mitochondrial Trifunctional Protein Deficiency.