Overview
Gustavo Ferreira practices practicing medicine in Criciuma, Brazil.
Ferreira is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Maple Syrup Urine Disease, Tyrosinemia Type 2, Malonyl-CoA Decarboxylase Deficiency, and Hereditary Fructose Intolerance.
They are actively involved in clinical research, co-authoring 85 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 Gustavo C. Ferreira
Is Gustavo C. Ferreira a top-rated expert for Maple Syrup Urine Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Gustavo C. Ferreira is classified as an Distinguished 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 Gustavo C. Ferreira participate in research or clinical trials?
Yes. Gustavo C. Ferreira has published 85 articles and abstracts on conditions like Maple Syrup Urine Disease. You can view a list of Gustavo C. Ferreira'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
- Maple Syrup Urine DiseaseFerreira isDistinguished. Learn about Maple Syrup Urine Disease.
- Tyrosinemia Type 2Ferreira isDistinguished. Learn about Tyrosinemia Type 2.
- Advanced
- Malonyl-CoA Decarboxylase Deficiency
- Experienced
- Acute Kidney FailureFerreira isExperienced. Learn about Acute Kidney Failure.
- Childhood PancreatitisFerreira isExperienced. Learn about Childhood Pancreatitis.
- Embryonal Tumor with Multilayered Rosettes
- GalactosemiaFerreira isExperienced. Learn about Galactosemia.
- Hereditary Fructose IntoleranceFerreira isExperienced. Learn about Hereditary Fructose Intolerance.
- Memory LossFerreira isExperienced. Learn about Memory Loss.
- Methylmalonic AcidemiaFerreira isExperienced. Learn about Methylmalonic Acidemia.
- NeuroblastomaFerreira isExperienced. Learn about Neuroblastoma.
- Phenylketonuria (PKU)Ferreira isExperienced. Learn about Phenylketonuria (PKU).
- Severe Acute Respiratory Syndrome (SARS)