Overview
Dawn Cordeiro practices practicing medicine in Toronto, Canada.
Ms. Cordeiro is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Mitochondrial Complex 2 Deficiency, PMM2-Congenital Disorder of Glycosylation, Coenzyme Q Cytochrome C Reductase Deficiency, and Sialuria.
She is actively involved in clinical research, co-authoring 18 peer reviewed articles.
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 Dawn Cordeiro
Is Dawn Cordeiro a top-rated expert for Mitochondrial Complex 2 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dawn Cordeiro 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 Dawn Cordeiro participate in research or clinical trials?
Yes. Dawn Cordeiro has published 18 articles and abstracts on conditions like Mitochondrial Complex 2 Deficiency. You can view a list of Dawn Cordeiro'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
- Mitochondrial Complex 2 DeficiencyMs. Cordeiro isAdvanced. Learn about Mitochondrial Complex 2 Deficiency.
- Experienced
- Absence SeizureMs. Cordeiro isExperienced. Learn about Absence Seizure.
- Coenzyme Q Cytochrome C Reductase Deficiency
- EpilepsyMs. Cordeiro isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenMs. Cordeiro isExperienced. Learn about Epilepsy in Children.
- Generalized Tonic-Clonic SeizureMs. Cordeiro isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Movement DisordersMs. Cordeiro isExperienced. Learn about Movement Disorders.
- PMM2-Congenital Disorder of GlycosylationMs. Cordeiro isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- SeizuresMs. Cordeiro isExperienced. Learn about Seizures.
- Sialic Acid Storage DiseaseMs. Cordeiro isExperienced. Learn about Sialic Acid Storage Disease.
- SialuriaMs. Cordeiro isExperienced. Learn about Sialuria.
- X-Linked Creatine DeficiencyMs. Cordeiro isExperienced. Learn about X-Linked Creatine Deficiency.