Overview
Jamiyan Purevsuren practices practicing medicine in Izumo, Japan.
Purevsuren is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Glutaric Acidemia Type 2, Argininosuccinic Aciduria, Maternal Hyperphenylalaninemia, and Inborn Amino Acid Metabolism Disorder.
They are actively involved in clinical research, co-authoring 15 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 Jamiyan Purevsuren
Is Jamiyan Purevsuren a top-rated expert for Glutaric Acidemia Type 2?
MediFind is an objective health platform that identifies experts based on real-world data. Jamiyan Purevsuren is classified as an Advanced expert for Glutaric Acidemia Type 2, 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 Jamiyan Purevsuren participate in research or clinical trials?
Yes. Jamiyan Purevsuren has published 15 articles and abstracts on conditions like Glutaric Acidemia Type 2. You can view a list of Jamiyan Purevsuren'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
- Advanced
- Argininosuccinic AciduriaPurevsuren isAdvanced. Learn about Argininosuccinic Aciduria.
- Glutaric Acidemia Type 2Purevsuren isAdvanced. Learn about Glutaric Acidemia Type 2.
- Experienced
- CitrullinemiaPurevsuren isExperienced. Learn about Citrullinemia.
- Congenital HypothyroidismPurevsuren isExperienced. Learn about Congenital Hypothyroidism.
- HomocystinuriaPurevsuren isExperienced. Learn about Homocystinuria.
- HypothyroidismPurevsuren isExperienced. Learn about Hypothyroidism.
- HypotoniaPurevsuren isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderPurevsuren isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseasePurevsuren isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaPurevsuren isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaPurevsuren isExperienced. Learn about Methylmalonic Acidemia.
- Multiple Carboxylase DeficiencyPurevsuren isExperienced. Learn about Multiple Carboxylase Deficiency.
- Neonatal HypothyroidismPurevsuren isExperienced. Learn about Neonatal Hypothyroidism.
- Phenylketonuria (PKU)Purevsuren isExperienced. Learn about Phenylketonuria (PKU).
- Primary Carnitine DeficiencyPurevsuren isExperienced. Learn about Primary Carnitine Deficiency.
- Primary Lateral SclerosisPurevsuren isExperienced. Learn about Primary Lateral Sclerosis.
- Propionic AcidemiaPurevsuren isExperienced. Learn about Propionic Acidemia.
- Urea Cycle Disorders (UCD)Purevsuren isExperienced. Learn about Urea Cycle Disorders (UCD).