Overview
Anita Macdonald practices in Birmingham, United Kingdom. Ms. Macdonald is highly rated in 12 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Tyrosinemia Type 1, Gastrostomy, and Liver Embolization.
Her clinical research consists of co-authoring 237 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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 Anita J. Macdonald
Is Anita J. Macdonald a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Anita J. Macdonald is classified as an Elite 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 Anita J. Macdonald participate in research or clinical trials?
Yes. Anita J. Macdonald has published 236 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Anita J. Macdonald'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
- Elite
- Phenylketonuria (PKU)Ms. Macdonald isElite. Learn about Phenylketonuria (PKU).
- Distinguished
- Carnitine-Acylcarnitine Translocase DeficiencyMs. Macdonald isDistinguished. Learn about Carnitine-Acylcarnitine Translocase Deficiency.
- Classic GalactosemiaMs. Macdonald isDistinguished. Learn about Classic Galactosemia.
- Maternal HyperphenylalaninemiaMs. Macdonald isDistinguished. Learn about Maternal Hyperphenylalaninemia.
- Tyrosinemia Type 1Ms. Macdonald isDistinguished. Learn about Tyrosinemia Type 1.
- Advanced
- Argininosuccinic AciduriaMs. Macdonald isAdvanced. Learn about Argininosuccinic Aciduria.
- GalactosemiaMs. Macdonald isAdvanced. Learn about Galactosemia.
- Isovaleric AcidemiaMs. Macdonald isAdvanced. Learn about Isovaleric Acidemia.
- Metabolic AcidosisMs. Macdonald isAdvanced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaMs. Macdonald isAdvanced. Learn about Methylmalonic Acidemia.
- Propionic AcidemiaMs. Macdonald isAdvanced. Learn about Propionic Acidemia.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Brachydactyly Mononen TypeMs. Macdonald isExperienced. Learn about Brachydactyly Mononen Type.
- CitrullinemiaMs. Macdonald isExperienced. Learn about Citrullinemia.
- Enlarged LiverMs. Macdonald isExperienced. Learn about Enlarged Liver.
- Familial Adenomatous PolyposisMs. Macdonald isExperienced. Learn about Familial Adenomatous Polyposis.
- Fructose-1,6-Bisphosphatase DeficiencyMs. Macdonald isExperienced. Learn about Fructose-1,6-Bisphosphatase Deficiency.