Overview
Maria Fuller practices practicing medicine in Adelaide, Australia.
Ms. Fuller is highly rated in 12 conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Lipogranulomatosis, and Gaucher Disease.
She is actively involved in clinical research, co-authoring 87 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 Maria Fuller
Is Maria Fuller a top-rated expert for Mucopolysaccharidoses (MPS)?
MediFind is an objective health platform that identifies experts based on real-world data. Maria Fuller is classified as an Distinguished 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 Maria Fuller participate in research or clinical trials?
Yes. Maria Fuller has published 87 articles and abstracts on conditions like Mucopolysaccharidoses (MPS). You can view a list of Maria Fuller'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
- Distinguished
- Gaucher DiseaseMs. Fuller isDistinguished. Learn about Gaucher Disease.
- LipogranulomatosisMs. Fuller isDistinguished. Learn about Lipogranulomatosis.
- Mucopolysaccharidoses (MPS)Ms. Fuller isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Advanced
- Fabry DiseaseMs. Fuller isAdvanced. Learn about Fabry Disease.
- Farber LipogranulomatosisMs. Fuller isAdvanced. Learn about Farber Lipogranulomatosis.
- Fetal EdemaMs. Fuller isAdvanced. Learn about Fetal Edema.
- Gaucher Disease Type 1Ms. Fuller isAdvanced. Learn about Gaucher Disease Type 1.
- Hydrops FetalisMs. Fuller isAdvanced. Learn about Hydrops Fetalis.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyMs. Fuller isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Experienced
- Alpha ThalassemiaMs. Fuller isExperienced. Learn about Alpha Thalassemia.
- Barth SyndromeMs. Fuller isExperienced. Learn about Barth Syndrome.
- Batten DiseaseMs. Fuller isExperienced. Learn about Batten Disease.
- Bile Duct ObstructionMs. Fuller isExperienced. Learn about Bile Duct Obstruction.
- Brachydactyly Mononen TypeMs. Fuller isExperienced. Learn about Brachydactyly Mononen Type.
- CACH SyndromeMs. Fuller isExperienced. Learn about CACH Syndrome.
- CardiomyopathyMs. Fuller isExperienced. Learn about Cardiomyopathy.
- CholestasisMs. Fuller isExperienced. Learn about Cholestasis.
- CLN1 DiseaseMs. Fuller isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Fuller isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Fuller isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Fuller isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Fuller isExperienced. Learn about CLN5 Disease.
- Dentatorubral-Pallidoluysian AtrophyMs. Fuller isExperienced. Learn about Dentatorubral-Pallidoluysian Atrophy.
- Enlarged LiverMs. Fuller isExperienced. Learn about Enlarged Liver.
- GangliosidosisMs. Fuller isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMs. Fuller isExperienced. Learn about GM1 Gangliosidosis.
- HemoglobinopathyMs. Fuller isExperienced. Learn about Hemoglobinopathy.
- Hemolytic Disease of the NewbornMs. Fuller isExperienced. Learn about Hemolytic Disease of the Newborn.
- Intrahepatic Cholestasis of PregnancyMs. Fuller isExperienced. Learn about Intrahepatic Cholestasis of Pregnancy.
- Krabbe DiseaseMs. Fuller isExperienced. Learn about Krabbe Disease.
- Lafora DiseaseMs. Fuller isExperienced. Learn about Lafora Disease.
- LeukodystrophyMs. Fuller isExperienced. Learn about Leukodystrophy.
- Maple Syrup Urine DiseaseMs. Fuller isExperienced. Learn about Maple Syrup Urine Disease.
- Metachromatic LeukodystrophyMs. Fuller isExperienced. Learn about Metachromatic Leukodystrophy.
- Mucolipidosis Type 4Ms. Fuller isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Myoclonic EpilepsyMs. Fuller isExperienced. Learn about Myoclonic Epilepsy.
- Niemann-Pick DiseaseMs. Fuller isExperienced. Learn about Niemann-Pick Disease.
- Palatal MyoclonusMs. Fuller isExperienced. Learn about Palatal Myoclonus.
- Phenylketonuria (PKU)Ms. Fuller isExperienced. Learn about Phenylketonuria (PKU).
- Pompe DiseaseMs. Fuller isExperienced. Learn about Pompe Disease.
- Primary Lateral SclerosisMs. Fuller isExperienced. Learn about Primary Lateral Sclerosis.
- Sialic Acid Storage DiseaseMs. Fuller isExperienced. Learn about Sialic Acid Storage Disease.
- SialuriaMs. Fuller isExperienced. Learn about Sialuria.
- Tay-Sachs DiseaseMs. Fuller isExperienced. Learn about Tay-Sachs Disease.
- ThalassemiaMs. Fuller isExperienced. Learn about Thalassemia.