Overview
Serena Gasperini practices in Monza, Italy. Ms. Gasperini is rated as an Advanced expert by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Arginase Deficiency, Urea Cycle Disorders (UCD), and Liver Transplant.
Her clinical research consists of co-authoring 79 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Carbamoyl Phosphate Synthetase 1 Deficiency.
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
- Arginase DeficiencyMs. Gasperini isDistinguished. Learn about Arginase Deficiency.
- Mucopolysaccharidoses (MPS)Ms. Gasperini isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Advanced
- Argininosuccinic AciduriaMs. Gasperini isAdvanced. Learn about Argininosuccinic Aciduria.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Glycogen Storage Disease Type 0Ms. Gasperini isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 3Ms. Gasperini isAdvanced. Learn about Glycogen Storage Disease Type 3.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Gasperini isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- AgranulocytosisMs. Gasperini isExperienced. Learn about Agranulocytosis.
- Barth SyndromeMs. Gasperini isExperienced. Learn about Barth Syndrome.
- Beta-Propeller Protein-Associated Neurodegeneration
- Brachydactyly Mononen TypeMs. Gasperini isExperienced. Learn about Brachydactyly Mononen Type.
- CardiomyopathyMs. Gasperini isExperienced. Learn about Cardiomyopathy.