Overview
Vanusa Manfredini practices practicing medicine in Uruguaiana, Brazil.
Manfredini is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Maple Syrup Urine Disease, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, L-2-Hydroxyglutaric Aciduria, and Hypermethioninemia.
They are actively involved in clinical research, co-authoring 59 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 Vanusa Manfredini
Is Vanusa Manfredini a top-rated expert for Maple Syrup Urine Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Vanusa Manfredini is classified as an Advanced expert for Maple Syrup Urine 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 Vanusa Manfredini participate in research or clinical trials?
Yes. Vanusa Manfredini has published 59 articles and abstracts on conditions like Maple Syrup Urine Disease. You can view a list of Vanusa Manfredini'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
- Maple Syrup Urine DiseaseManfredini isAdvanced. Learn about Maple Syrup Urine Disease.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Abdominal Obesity Metabolic SyndromeManfredini isExperienced. Learn about Abdominal Obesity Metabolic Syndrome.
- Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency
- Glutaric Acidemia Type 1Manfredini isExperienced. Learn about Glutaric Acidemia Type 1.
- HypermethioninemiaManfredini isExperienced. Learn about Hypermethioninemia.
- L-2-Hydroxyglutaric AciduriaManfredini isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.
- MalabsorptionManfredini isExperienced. Learn about Malabsorption.
- MalnutritionManfredini isExperienced. Learn about Malnutrition.
- Memory LossManfredini isExperienced. Learn about Memory Loss.
- Metabolic SyndromeManfredini isExperienced. Learn about Metabolic Syndrome.
- Methylmalonic AcidemiaManfredini isExperienced. Learn about Methylmalonic Acidemia.
- ObesityManfredini isExperienced. Learn about Obesity.
- Ocular ToxoplasmosisManfredini isExperienced. Learn about Ocular Toxoplasmosis.
- Propionic AcidemiaManfredini isExperienced. Learn about Propionic Acidemia.