Overview
Graeme Nimmo practices in Toronto, Canada. Mr. Nimmo is rated as an Advanced expert by MediFind in the treatment of Mitochondrial Complex 2 Deficiency. His top areas of expertise are Mitochondrial Complex 2 Deficiency, Gaucher Disease Type 1, Coenzyme Q Cytochrome C Reductase Deficiency, and Pyruvate Decarboxylase Deficiency.
His clinical research consists of co-authoring 16 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Mitochondrial Complex 2 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
- Coenzyme Q Cytochrome C Reductase Deficiency
- Gaucher Disease Type 1Mr. Nimmo isAdvanced. Learn about Gaucher Disease Type 1.
- Mitochondrial Complex 2 Deficiency
- Experienced
- AchondrogenesisMr. Nimmo isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Nimmo isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Chondrodysplasia Punctata SyndromeMr. Nimmo isExperienced. Learn about Chondrodysplasia Punctata Syndrome.