Overview
Heidi Peters practices practicing medicine in Melbourne, Australia.
Ms. Peters is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Leigh Syndrome, Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and Riboflavin Transporter Deficiency Neuronopathy.
She is actively involved in clinical research, co-authoring 41 peer reviewed articles and participating in 2 clinical trials.
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.
2 Clinical Trials
Frequently Asked Questions about Heidi L. Peters
Is Heidi L. Peters a top-rated expert for Leigh Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Heidi L. Peters is classified as an Advanced expert for Leigh Syndrome, 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 Heidi L. Peters participate in research or clinical trials?
Yes. Heidi L. Peters has published 41 articles and abstracts on conditions like Leigh Syndrome. You can view a list of Heidi L. Peters'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
- Leigh SyndromeMs. Peters isAdvanced. Learn about Leigh Syndrome.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Pyruvate Decarboxylase DeficiencyMs. Peters isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Peters isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Riboflavin Transporter Deficiency Neuronopathy
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Peters isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Alternating Hemiplegia of ChildhoodMs. Peters isExperienced. Learn about Alternating Hemiplegia of Childhood.
- CACH SyndromeMs. Peters isExperienced. Learn about CACH Syndrome.
- Dihydrolipoamide Dehydrogenase Deficiency
- Early Infantile Epileptic Encephalopathy
- Fabry DiseaseMs. Peters isExperienced. Learn about Fabry Disease.
- Gaucher DiseaseMs. Peters isExperienced. Learn about Gaucher Disease.
- HemiplegiaMs. Peters isExperienced. Learn about Hemiplegia.
- HistiocytosisMs. Peters isExperienced. Learn about Histiocytosis.
- HypotoniaMs. Peters isExperienced. Learn about Hypotonia.
- Infantile Axonal NeuropathyMs. Peters isExperienced. Learn about Infantile Axonal Neuropathy.
- Liver FailureMs. Peters isExperienced. Learn about Liver Failure.
- Metabolic AcidosisMs. Peters isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaMs. Peters isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidoses (MPS)Ms. Peters isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Multiple Sulfatase DeficiencyMs. Peters isExperienced. Learn about Multiple Sulfatase Deficiency.
- Niemann-Pick DiseaseMs. Peters isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMs. Peters isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Ornithine Transcarbamylase DeficiencyMs. Peters isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Ms. Peters isExperienced. Learn about Phenylketonuria (PKU).
- Pompe DiseaseMs. Peters isExperienced. Learn about Pompe Disease.
- Primary Lateral SclerosisMs. Peters isExperienced. Learn about Primary Lateral Sclerosis.
- ReticulohistiocytomaMs. Peters isExperienced. Learn about Reticulohistiocytoma.
- RhabdomyolysisMs. Peters isExperienced. Learn about Rhabdomyolysis.
- Urea Cycle Disorders (UCD)Ms. Peters isExperienced. Learn about Urea Cycle Disorders (UCD).