Overview
Peter Currie practices in Clayton, Australia. Mr. Currie is rated as a Distinguished expert by MediFind in the treatment of Congenital Muscular Dystrophy Type 1A. His top areas of expertise are Congenital Muscular Dystrophy Type 1A, Benign Autosomal Dominant Myopathy, Limb-Girdle Muscular Dystrophy Type 2I, and Klippel-Feil Syndrome.
His clinical research consists of co-authoring 100 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Congenital Muscular Dystrophy Type 1A.
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
- Distinguished
- Congenital Muscular Dystrophy Type 1AMr. Currie isDistinguished. Learn about Congenital Muscular Dystrophy Type 1A.
- Experienced
- Becker Muscular DystrophyMr. Currie isExperienced. Learn about Becker Muscular Dystrophy.
- Benign Autosomal Dominant MyopathyMr. Currie isExperienced. Learn about Benign Autosomal Dominant Myopathy.
- Collagen VI-Related MyopathyMr. Currie isExperienced. Learn about Collagen VI-Related Myopathy.
- Congenital Fiber-Type DisproportionMr. Currie isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Duchenne Muscular DystrophyMr. Currie isExperienced. Learn about Duchenne Muscular Dystrophy.
- Frontonasal Dysplasia Klippel Feil Syndrome