Overview
John Mitchell practices practicing medicine in Montreal, Canada.
Mr. Mitchell is highly rated in 10 conditions, according to our data. His clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Lipogranulomatosis, Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), and Mucopolysaccharidoses (MPS).
He is actively involved in clinical research, co-authoring 74 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 John J. Mitchell
Is John J. Mitchell 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. John J. Mitchell 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 John J. Mitchell participate in research or clinical trials?
Yes. John J. Mitchell has published 74 articles and abstracts on conditions like Medium-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of John J. Mitchell'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
- LipogranulomatosisMr. Mitchell isDistinguished. Learn about Lipogranulomatosis.
- Mucopolysaccharidoses (MPS)Mr. Mitchell isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Advanced
- Agenesis of the Dorsal PancreasMr. Mitchell isAdvanced. Learn about Agenesis of the Dorsal Pancreas.
- Brachydactyly Mononen TypeMr. Mitchell isAdvanced. Learn about Brachydactyly Mononen Type.
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Multiple Sulfatase DeficiencyMr. Mitchell isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Phenylketonuria (PKU)Mr. Mitchell isAdvanced. Learn about Phenylketonuria (PKU).
- Von Gierke DiseaseMr. Mitchell isAdvanced. Learn about Von Gierke Disease.
- Experienced
- Dentatorubral-Pallidoluysian AtrophyMr. Mitchell isExperienced. Learn about Dentatorubral-Pallidoluysian Atrophy.
- Farber LipogranulomatosisMr. Mitchell isExperienced. Learn about Farber Lipogranulomatosis.
- HivesMr. Mitchell isExperienced. Learn about Hives.
- Lafora DiseaseMr. Mitchell isExperienced. Learn about Lafora Disease.
- LeukodystrophyMr. Mitchell isExperienced. Learn about Leukodystrophy.
- Low Blood SugarMr. Mitchell isExperienced. Learn about Low Blood Sugar.
- Maternal HyperphenylalaninemiaMr. Mitchell isExperienced. Learn about Maternal Hyperphenylalaninemia.
- MosaicismMr. Mitchell isExperienced. Learn about Mosaicism.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Myoclonic EpilepsyMr. Mitchell isExperienced. Learn about Myoclonic Epilepsy.
- Newborn Low Blood SugarMr. Mitchell isExperienced. Learn about Newborn Low Blood Sugar.
- Primary Lateral SclerosisMr. Mitchell isExperienced. Learn about Primary Lateral Sclerosis.
- Progressive Myoclonic EpilepsyMr. Mitchell isExperienced. Learn about Progressive Myoclonic Epilepsy.