Overview
Chitra Prasad practices practicing medicine in London, Canada.
Ms. Prasad is highly rated in 15 conditions, according to our data. Her clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Micrognathia, Nicolaides-Baraitser Syndrome, and Urea Cycle Disorders (UCD).
She is actively involved in clinical research, co-authoring 109 peer reviewed articles and participating in 1 clinical trial.
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.
1 Clinical Trials
Frequently Asked Questions about Chitra K. Prasad
Is Chitra K. Prasad 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. Chitra K. Prasad 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 Chitra K. Prasad participate in research or clinical trials?
Yes. Chitra K. Prasad has published 109 articles and abstracts on conditions like Medium-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Chitra K. Prasad'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
- Advanced
- Cortical DysplasiaMs. Prasad isAdvanced. Learn about Cortical Dysplasia.
- Enlarged LiverMs. Prasad isAdvanced. Learn about Enlarged Liver.
- Fumarase DeficiencyMs. Prasad isAdvanced. Learn about Fumarase Deficiency.
- Galloway-Mowat SyndromeMs. Prasad isAdvanced. Learn about Galloway-Mowat Syndrome.
- HypotoniaMs. Prasad isAdvanced. Learn about Hypotonia.
- MELAS SyndromeMs. Prasad isAdvanced. Learn about MELAS Syndrome.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- AbetalipoproteinemiaMs. Prasad isExperienced. Learn about Abetalipoproteinemia.
- Achalasia Microcephaly SyndromeMs. Prasad isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AcheiropodyMs. Prasad isExperienced. Learn about Acheiropody.
- Acute Cerebellar AtaxiaMs. Prasad isExperienced. Learn about Acute Cerebellar Ataxia.
- Acute Hepatic Porphyria (AHP)Ms. Prasad isExperienced. Learn about Acute Hepatic Porphyria (AHP).