Overview
Peter Sharp practices practicing medicine in Cobbitty, Australia.
His clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Multiple Sulfatase Deficiency.
He is actively involved in clinical research, co-authoring 13 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 Peter J. Sharp
Is Peter J. Sharp a top-rated expert for Mucopolysaccharidoses (MPS)?
MediFind is an objective health platform that identifies experts based on real-world data. Peter J. Sharp is classified as an Experienced expert for Mucopolysaccharidoses (MPS), 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 Peter J. Sharp participate in research or clinical trials?
Yes. Peter J. Sharp has published 13 articles and abstracts on conditions like Mucopolysaccharidoses (MPS). You can view a list of Peter J. Sharp'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
- Experienced
- Mucopolysaccharidoses (MPS)Mr. Sharp isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Multiple Sulfatase DeficiencyMr. Sharp isExperienced. Learn about Multiple Sulfatase Deficiency.