Overview
Anastasia Ambrose practices in Edmonton, Canada. Ms. Ambrose is rated as an Experienced expert by MediFind in the treatment of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Her top areas of expertise are Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, PGM1-CDG, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Aminoaciduria.
Her clinical research consists of co-authoring 8 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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.
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
- Experienced
- AminoaciduriaMs. Ambrose isExperienced. Learn about Aminoaciduria.
- Cerebellar HypoplasiaMs. Ambrose isExperienced. Learn about Cerebellar Hypoplasia.
- Congenital Fiber-Type DisproportionMs. Ambrose isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Fanconi Bickel SyndromeMs. Ambrose isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMs. Ambrose isExperienced. Learn about Fanconi Syndrome.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency