Overview
Beth Potter practices practicing medicine in Ottawa, Canada.
Ms. Potter is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Phenylketonuria (PKU), Guanidinoacetate Methyltransferase Deficiency, and X-Linked Creatine Deficiency.
She is actively involved in clinical research, co-authoring 150 peer reviewed articles.
Gender
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. 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.
Frequently Asked Questions about Beth K. Potter
Is Beth K. Potter a top-rated expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Beth K. Potter is classified as an Elite expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Beth K. Potter participate in research or clinical trials?
Yes. Beth K. Potter has published 149 articles and abstracts on conditions like Medium-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Beth K. Potter's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Distinguished
- Phenylketonuria (PKU)Ms. Potter isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Guanidinoacetate Methyltransferase Deficiency
- X-Linked Creatine DeficiencyMs. Potter isAdvanced. Learn about X-Linked Creatine Deficiency.
- Experienced
- Bilirubin EncephalopathyMs. Potter isExperienced. Learn about Bilirubin Encephalopathy.
- Breast CancerMs. Potter isExperienced. Learn about Breast Cancer.
- Colorectal CancerMs. Potter isExperienced. Learn about Colorectal Cancer.
- Congenital HypothyroidismMs. Potter isExperienced. Learn about Congenital Hypothyroidism.
- Cystic FibrosisMs. Potter isExperienced. Learn about Cystic Fibrosis.
- Down SyndromeMs. Potter isExperienced. Learn about Down Syndrome.
- Dravet SyndromeMs. Potter isExperienced. Learn about Dravet Syndrome.
- EpilepsyMs. Potter isExperienced. Learn about Epilepsy.
- Hemolytic Disease of the NewbornMs. Potter isExperienced. Learn about Hemolytic Disease of the Newborn.
- MelanomaMs. Potter isExperienced. Learn about Melanoma.
- Mucopolysaccharidoses (MPS)Ms. Potter isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Myoclonic EpilepsyMs. Potter isExperienced. Learn about Myoclonic Epilepsy.
- Neonatal HypothyroidismMs. Potter isExperienced. Learn about Neonatal Hypothyroidism.
- Primary Lateral SclerosisMs. Potter isExperienced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)Ms. Potter isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 2Ms. Potter isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Ms. Potter isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Trisomy 18Ms. Potter isExperienced. Learn about Trisomy 18.