Overview
Sabrina Mackinnon practices in Newcastle Upon Tyne, United Kingdom. Ms. Mackinnon is rated as an Experienced expert by MediFind in the treatment of Galactokinase Deficiency. Her top areas of expertise are Classic Galactosemia, Primary Hyperoxaluria, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, and Galactose Epimerase Deficiency.
Her clinical research consists of co-authoring 10 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Galactokinase Deficiency.
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.
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
- Classic GalactosemiaMs. Mackinnon isAdvanced. Learn about Classic Galactosemia.
- Primary HyperoxaluriaMs. Mackinnon isAdvanced. Learn about Primary Hyperoxaluria.
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
- Experienced
- Galactokinase DeficiencyMs. Mackinnon isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Mackinnon isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Mackinnon isExperienced. Learn about Galactosemia.
- Metabolic AcidosisMs. Mackinnon isExperienced. Learn about Metabolic Acidosis.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Primary Hyperoxaluria Type 1Ms. Mackinnon isExperienced. Learn about Primary Hyperoxaluria Type 1.