Overview
Bruna Ferreira practices practicing medicine in Criciuma, Brazil.
Ms. Ferreira is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Malonyl-CoA Decarboxylase Deficiency, Hereditary Fructose Intolerance, Galactosemia, and Phenylketonuria (PKU).
She is actively involved in clinical research, co-authoring 14 peer reviewed articles.
Gender
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 Bruna K. Ferreira
Is Bruna K. Ferreira a top-rated expert for Malonyl-CoA Decarboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Bruna K. Ferreira is classified as an Advanced expert for Malonyl-CoA Decarboxylase Deficiency, 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 Bruna K. Ferreira participate in research or clinical trials?
Yes. Bruna K. Ferreira has published 14 articles and abstracts on conditions like Malonyl-CoA Decarboxylase Deficiency. You can view a list of Bruna K. 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
- Advanced
- Malonyl-CoA Decarboxylase DeficiencyMs. Ferreira isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Experienced
- GalactosemiaMs. Ferreira isExperienced. Learn about Galactosemia.
- Hereditary Fructose IntoleranceMs. Ferreira isExperienced. Learn about Hereditary Fructose Intolerance.
- Phenylketonuria (PKU)Ms. Ferreira isExperienced. Learn about Phenylketonuria (PKU).