Dr. Angelika Erwin
Overview
Angelika Erwin is a Pediatrics provider in Cleveland, Ohio. Dr. Erwin is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Gaucher Disease Type 2, Gaucher Disease, Gaucher Disease Type 3, and Gaucher Disease Type 1.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- MEDICARE SNP
- MEDICARE MAPD
- OTHER MEDICARE
- EPO
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- OTHER MANAGED MEDICAID
- HMO
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- INDEMNITY
- PPO
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE PART D
- MEDICARE SNP
- HMO
- PPO
- HMO
- MANAGED MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- EPO
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
9620 Carnegie Avenue, Cleveland, OH 44106
University Hospitals Medical Group Inc
Suzanne Debrosse is a Medical Genetics specialist and a Pediatrics provider in Cleveland, Ohio. Dr. Debrosse is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, Dihydrolipoamide Dehydrogenase Deficiency, and PEPCK 1 Deficiency. Dr. Debrosse is currently accepting new patients.
Cleveland Clinic Main Campus
Elia Knight is a Pediatrics provider in Cleveland, Ohio. Dr. Knight is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Epilepsy in Children, Genetic Epilepsy with Febrile Seizures Plus (GEFS+), Wildervanck Syndrome, and Microcephaly Deafness Syndrome.
University Primary Care Practices Inc
Jennifer Carandang is a primary care provider, practicing in Pediatrics and Internal Medicine in Conneaut, Ohio. Dr. Carandang is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Vitamin D Deficiency, Vitamin B12 Deficiency Anemia, Folate Deficiency, and Multiple Carboxylase Deficiency. Dr. Carandang 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
- Distinguished
- Gaucher DiseaseDr. Erwin isDistinguished. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Erwin isDistinguished. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Erwin isDistinguished. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Erwin isDistinguished. Learn about Gaucher Disease Type 3.
- Advanced
- Fabry DiseaseDr. Erwin isAdvanced. Learn about Fabry Disease.
- Niemann-Pick DiseaseDr. Erwin isAdvanced. Learn about Niemann-Pick Disease.
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy
- Pompe DiseaseDr. Erwin isAdvanced. Learn about Pompe Disease.
- Experienced
- Amniotic Band SyndromeDr. Erwin isExperienced. Learn about Amniotic Band Syndrome.
- Ehlers-Danlos Syndrome (EDS)Dr. Erwin isExperienced. Learn about Ehlers-Danlos Syndrome (EDS).
- Hereditary AtaxiaDr. Erwin isExperienced. Learn about Hereditary Ataxia.
- Hereditary Spastic ParaparesisDr. Erwin isExperienced. Learn about Hereditary Spastic Paraparesis.
- Mucopolysaccharidoses (MPS)Dr. Erwin isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)