Overview
Jagdeep Walia practices practicing medicine in Kingston, Canada.
Mr. Walia is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Sandhoff Disease, Tay-Sachs Disease, Gangliosidosis, and Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
He is actively involved in clinical research, co-authoring 52 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 Jagdeep S. Walia
Is Jagdeep S. Walia a top-rated expert for Sandhoff Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Jagdeep S. Walia is classified as an Elite expert for Sandhoff Disease, 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 Jagdeep S. Walia participate in research or clinical trials?
Yes. Jagdeep S. Walia has published 52 articles and abstracts on conditions like Sandhoff Disease. You can view a list of Jagdeep S. Walia'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
- GangliosidosisMr. Walia isElite. Learn about Gangliosidosis.
- Sandhoff DiseaseMr. Walia isElite. Learn about Sandhoff Disease.
- Tay-Sachs DiseaseMr. Walia isElite. Learn about Tay-Sachs Disease.
- Distinguished
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Advanced
- Ornithine Translocase Deficiency
- Experienced
- Achard SyndromeMr. Walia isExperienced. Learn about Achard Syndrome.
- Alpha ThalassemiaMr. Walia isExperienced. Learn about Alpha Thalassemia.
- ArachnodactylyMr. Walia isExperienced. Learn about Arachnodactyly.
- Congenital Contractural Arachnodactyly
- Crouzon SyndromeMr. Walia isExperienced. Learn about Crouzon Syndrome.
- Drug Induced DyskinesiaMr. Walia isExperienced. Learn about Drug Induced Dyskinesia.
- EpilepsyMr. Walia isExperienced. Learn about Epilepsy.
- Fetal EdemaMr. Walia isExperienced. Learn about Fetal Edema.
- Gaucher DiseaseMr. Walia isExperienced. Learn about Gaucher Disease.
- Guanidinoacetate Methyltransferase Deficiency
- Hemolytic Disease of the NewbornMr. Walia isExperienced. Learn about Hemolytic Disease of the Newborn.
- Hydrops FetalisMr. Walia isExperienced. Learn about Hydrops Fetalis.
- HypotoniaMr. Walia isExperienced. Learn about Hypotonia.
- LipogranulomatosisMr. Walia isExperienced. Learn about Lipogranulomatosis.
- MacroglossiaMr. Walia isExperienced. Learn about Macroglossia.
- Patent Ductus ArteriosusMr. Walia isExperienced. Learn about Patent Ductus Arteriosus.
- Phenylketonuria (PKU)Mr. Walia isExperienced. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Mr. Walia isExperienced. Learn about Urea Cycle Disorders (UCD).