Overview
Simona Fecarotta practices in Naples, Italy. Ms. Fecarotta is highly rated in 7 conditions, according to our data. Her top areas of expertise are Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Pompe Disease, Mucopolysaccharidoses (MPS), and Wolman Disease.
Her clinical research consists of co-authoring 42 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.
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
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
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Advanced
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Fecarotta isAdvanced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Cholesteryl Ester Storage DiseaseMs. Fecarotta isAdvanced. Learn about Cholesteryl Ester Storage Disease.
- Lysosomal Acid Lipase DeficiencyMs. Fecarotta isAdvanced. Learn about Lysosomal Acid Lipase Deficiency.
- Mucopolysaccharidoses (MPS)Ms. Fecarotta isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Pompe DiseaseMs. Fecarotta isAdvanced. Learn about Pompe Disease.
- Wolman DiseaseMs. Fecarotta isAdvanced. Learn about Wolman Disease.
- Experienced
- Cortical DysplasiaMs. Fecarotta isExperienced. Learn about Cortical Dysplasia.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Fecarotta isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Fabry DiseaseMs. Fecarotta isExperienced. Learn about Fabry Disease.
- Fukuyama Type Muscular DystrophyMs. Fecarotta isExperienced. Learn about Fukuyama Type Muscular Dystrophy.
- Gaucher DiseaseMs. Fecarotta isExperienced. Learn about Gaucher Disease.
- Hereditary Fructose IntoleranceMs. Fecarotta isExperienced. Learn about Hereditary Fructose Intolerance.