Overview
Garry Brown practices practicing medicine in Oxford, United Kingdom.
Mr. Brown is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Pyruvate Dehydrogenase Deficiency, Pyruvate Decarboxylase Deficiency, Cytochrome C Oxidase Deficiency, and Dihydrolipoamide Dehydrogenase Deficiency.
He is actively involved in clinical research, co-authoring 26 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 Garry K. Brown
Is Garry K. Brown a top-rated expert for Pyruvate Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Garry K. Brown is classified as an Distinguished expert for Pyruvate 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 Garry K. Brown participate in research or clinical trials?
Yes. Garry K. Brown has published 26 articles and abstracts on conditions like Pyruvate Dehydrogenase Deficiency. You can view a list of Garry K. Brown'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
- Distinguished
- Pyruvate Decarboxylase DeficiencyMr. Brown isDistinguished. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Brown isDistinguished. Learn about Pyruvate Dehydrogenase Deficiency.
- Advanced
- Cytochrome C Oxidase DeficiencyMr. Brown isAdvanced. Learn about Cytochrome C Oxidase Deficiency.
- Dihydrolipoamide Dehydrogenase Deficiency
- Lactic AcidosisMr. Brown isAdvanced. Learn about Lactic Acidosis.
- Leigh SyndromeMr. Brown isAdvanced. Learn about Leigh Syndrome.
- Pyruvate Carboxylase DeficiencyMr. Brown isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Experienced
- Early Infantile Epileptic Encephalopathy
- Familial DysautonomiaMr. Brown isExperienced. Learn about Familial Dysautonomia.
- HypotoniaMr. Brown isExperienced. Learn about Hypotonia.
- MELAS SyndromeMr. Brown isExperienced. Learn about MELAS Syndrome.
- Multiple System AtrophyMr. Brown isExperienced. Learn about Multiple System Atrophy.
- Olivopontocerebellar AtrophyMr. Brown isExperienced. Learn about Olivopontocerebellar Atrophy.
- Pontocerebellar HypoplasiaMr. Brown isExperienced. Learn about Pontocerebellar Hypoplasia.
- Spastic Paraplegia Type 2Mr. Brown isExperienced. Learn about Spastic Paraplegia Type 2.
- Spinocerebellar AtaxiaMr. Brown isExperienced. Learn about Spinocerebellar Ataxia.
- West SyndromeMr. Brown isExperienced. Learn about West Syndrome.