Overview
Arthavan Selvanathan practices practicing medicine in Westmead, Australia.
Selvanathan is highly rated in 8 conditions, according to our data. Their clinical expertise encompasses Orotic Aciduria Type 1, Ornithine Transcarbamylase Deficiency, N-Acetylglutamate Synthase Deficiency, Urea Cycle Disorders (UCD), and Bone Marrow Transplant.
They are actively involved in clinical research, co-authoring 31 peer reviewed articles.
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 Arthavan Selvanathan
Is Arthavan Selvanathan a top-rated expert for Orotic Aciduria Type 1?
MediFind is an objective health platform that identifies experts based on real-world data. Arthavan Selvanathan is classified as an Elite expert for Orotic Aciduria Type 1, 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 Arthavan Selvanathan participate in research or clinical trials?
Yes. Arthavan Selvanathan has published 31 articles and abstracts on conditions like Orotic Aciduria Type 1. You can view a list of Arthavan Selvanathan'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
- Orotic Aciduria Type 1Selvanathan isElite. Learn about Orotic Aciduria Type 1.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Lactic AcidosisSelvanathan isAdvanced. Learn about Lactic Acidosis.
- Molybdenum Cofactor Deficiency (MoCD)
- N-Acetylglutamate Synthase Deficiency
- Ornithine Transcarbamylase Deficiency
- Sulfite Oxidase DeficiencySelvanathan isAdvanced. Learn about Sulfite Oxidase Deficiency.
- Urea Cycle Disorders (UCD)Selvanathan isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Experienced
- AspartylglucosaminuriaSelvanathan isExperienced. Learn about Aspartylglucosaminuria.
- Bone Marrow TransplantSelvanathan isExperienced. Learn about Bone Marrow Transplant.
- Cholesteryl Ester Storage DiseaseSelvanathan isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Enlarged LiverSelvanathan isExperienced. Learn about Enlarged Liver.
- Glycogen Storage Disease Type 9Selvanathan isExperienced. Learn about Glycogen Storage Disease Type 9.
- Lennox-Gastaut Syndrome (LGS)Selvanathan isExperienced. Learn about Lennox-Gastaut Syndrome (LGS).
- Metabolic AcidosisSelvanathan isExperienced. Learn about Metabolic Acidosis.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- RhabdomyolysisSelvanathan isExperienced. Learn about Rhabdomyolysis.
- Sideroblastic AnemiaSelvanathan isExperienced. Learn about Sideroblastic Anemia.
- Wolman DiseaseSelvanathan isExperienced. Learn about Wolman Disease.