Overview
Graeme Nimmo practices practicing medicine in Toronto, Canada.
Mr. Nimmo is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Mitochondrial Complex 2 Deficiency, Gaucher Disease Type 1, Coenzyme Q Cytochrome C Reductase Deficiency, and Gaucher Disease.
He is actively involved in clinical research, co-authoring 18 peer reviewed articles.
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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 Graeme M. Nimmo
Is Graeme M. Nimmo a top-rated expert for Mitochondrial Complex 2 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Graeme M. Nimmo is classified as an Advanced expert for Mitochondrial Complex 2 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 Graeme M. Nimmo participate in research or clinical trials?
Yes. Graeme M. Nimmo has published 18 articles and abstracts on conditions like Mitochondrial Complex 2 Deficiency. You can view a list of Graeme M. Nimmo'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
- Coenzyme Q Cytochrome C Reductase Deficiency
- Gaucher Disease Type 1Mr. Nimmo isAdvanced. Learn about Gaucher Disease Type 1.
- Mitochondrial Complex 2 Deficiency
- Experienced
- Gaucher DiseaseMr. Nimmo isExperienced. Learn about Gaucher Disease.
- Glycogen Storage Disease Type 5Mr. Nimmo isExperienced. Learn about Glycogen Storage Disease Type 5.
- Hallervorden-Spatz DiseaseMr. Nimmo isExperienced. Learn about Hallervorden-Spatz Disease.
- Mevalonate Kinase DeficiencyMr. Nimmo isExperienced. Learn about Mevalonate Kinase Deficiency.
- Movement DisordersMr. Nimmo isExperienced. Learn about Movement Disorders.
- Pantothenate Kinase-Associated Neurodegeneration
- Pyruvate Decarboxylase DeficiencyMr. Nimmo isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Nimmo isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Recessive Chondrodysplasia Punctata 1Mr. Nimmo isExperienced. Learn about Recessive Chondrodysplasia Punctata 1.