Anita MacDonald

Rare Disease Specialist

Birmingham Women's and Children's NHS Foundation Trust

Birmingham

PI on 10 trials

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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.

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Rare diseases treated or studied

Based on trial PI assignments and publication topics.

Glutaryl-CoA dehydrogenase deficiency
Maple syrup urine disease
Classic phenylketonuria
Tyrosinemia type 3
Central nervous system malformation
Homocystinuria
Tyrosinemia
Tyrosinemia type 1
Alkaptonuria
Phenylketonuria
Tyrosinemia type 2

Clinical trials (10)

NCT05995717
NCT06940193
NCT04196959
NCT05051657
NCT04076176
NCT03168399
NCT05096988
NCT03058848
NCT03913156
NCT06581991

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ClinicalTrials.gov PI search for Anita MacDonald

Other specialists for Glutaryl-CoA dehydrogenase deficiency

Peers ranked by clinical-trial PI role, publications, and verification quality.

Nicholas Ah Mew, MD
Children's National Research Institute
Laurent Servais
Centre Hospitalier Universitaire de Liege
Rulai Yang
The Children's Hospital Zhejiang University Shcool of Medicine
Qiang Shu
The Children's Hospital Zhejiang University Shcool of Medicine
Guanping Dong
The Children's Hospital Zhejiang University Shcool of Medicine
Leo G Visser, MD
Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands
Robert W. Sauerwein, MD
Radboud University Medical Center, Geert Grooteplein 28, 6525 GA Nijmegen, The Netherlands
Elena D Belousova, Prof
Veltischev Research and Clinical Institute for Pediatrics and Pediatric Surgery of the Pirogov Russian National Research Medical University

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