Overview
Daniella De Moura Coelho practices practicing medicine in Porto Alegre, Brazil.
Ms. De Moura Coelho is highly rated in 5 conditions, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Maple Syrup Urine Disease, Orotic Aciduria Type 1, and Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
She is actively involved in clinical research, co-authoring 16 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 Daniella De Moura Coelho
Is Daniella De Moura Coelho a top-rated expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Daniella De Moura Coelho is classified as an Advanced expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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 Daniella De Moura Coelho participate in research or clinical trials?
Yes. Daniella De Moura Coelho has published 16 articles and abstracts on conditions like 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. You can view a list of Daniella De Moura Coelho'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
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyMs. De Moura Coelho isAdvanced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Glutaric Acidemia Type 1Ms. De Moura Coelho isAdvanced. Learn about Glutaric Acidemia Type 1.
- Maple Syrup Urine DiseaseMs. De Moura Coelho isAdvanced. Learn about Maple Syrup Urine Disease.
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMs. De Moura Coelho isAdvanced. Learn about Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
- Orotic Aciduria Type 1Ms. De Moura Coelho isAdvanced. Learn about Orotic Aciduria Type 1.
- Experienced
- Addison's DiseaseMs. De Moura Coelho isExperienced. Learn about Addison's Disease.
- Adrenoleukodystrophy (ALD)Ms. De Moura Coelho isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Argininosuccinic AciduriaMs. De Moura Coelho isExperienced. Learn about Argininosuccinic Aciduria.
- CACH SyndromeMs. De Moura Coelho isExperienced. Learn about CACH Syndrome.
- Carbamoyl Phosphate Synthetase 1 DeficiencyMs. De Moura Coelho isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- L-2-Hydroxyglutaric AciduriaMs. De Moura Coelho isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.
- Metabolic AcidosisMs. De Moura Coelho isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaMs. De Moura Coelho isExperienced. Learn about Methylmalonic Acidemia.
- Phenylketonuria (PKU)Ms. De Moura Coelho isExperienced. Learn about Phenylketonuria (PKU).
- Primary Carnitine DeficiencyMs. De Moura Coelho isExperienced. Learn about Primary Carnitine Deficiency.
- Propionic AcidemiaMs. De Moura Coelho isExperienced. Learn about Propionic Acidemia.
- Urea Cycle Disorders (UCD)Ms. De Moura Coelho isExperienced. Learn about Urea Cycle Disorders (UCD).