Overview
Stuart Moat practices practicing medicine in Cardiff, United Kingdom.
Mr. Moat is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Isovaleric Acidemia, Homocystinuria, and Cystic Fibrosis.
He is actively involved in clinical research, co-authoring 49 peer reviewed articles.
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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 Stuart J. Moat
Is Stuart J. Moat a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Stuart J. Moat is classified as an Distinguished expert for Phenylketonuria (PKU), 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 Stuart J. Moat participate in research or clinical trials?
Yes. Stuart J. Moat has published 49 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Stuart J. Moat'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
- Phenylketonuria (PKU)Mr. Moat isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Isovaleric AcidemiaMr. Moat isAdvanced. Learn about Isovaleric Acidemia.
- Experienced
- AnemiaMr. Moat isExperienced. Learn about Anemia.
- Becker Muscular DystrophyMr. Moat isExperienced. Learn about Becker Muscular Dystrophy.
- Beta ThalassemiaMr. Moat isExperienced. Learn about Beta Thalassemia.
- Classic GalactosemiaMr. Moat isExperienced. Learn about Classic Galactosemia.
- Congenital Hemolytic AnemiaMr. Moat isExperienced. Learn about Congenital Hemolytic Anemia.
- Cystic FibrosisMr. Moat isExperienced. Learn about Cystic Fibrosis.
- Duchenne Muscular DystrophyMr. Moat isExperienced. Learn about Duchenne Muscular Dystrophy.
- Galactokinase DeficiencyMr. Moat isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Moat isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Moat isExperienced. Learn about Galactosemia.
- HemoglobinopathyMr. Moat isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaMr. Moat isExperienced. Learn about Hemolytic Anemia.
- HomocystinuriaMr. Moat isExperienced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR Deficiency
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseMr. Moat isExperienced. Learn about Maple Syrup Urine Disease.
- Mitochondrial Trifunctional Protein Deficiency
- Multiple Sclerosis (MS)Mr. Moat isExperienced. Learn about Multiple Sclerosis (MS).
- Protein DeficiencyMr. Moat isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMr. Moat isExperienced. Learn about Rhabdomyolysis.
- Severe Acute Respiratory Syndrome (SARS)
- Sickle Cell DiseaseMr. Moat isExperienced. Learn about Sickle Cell Disease.
- ThalassemiaMr. Moat isExperienced. Learn about Thalassemia.