Overview
Elisabetta Pasquini practices in Florence, Italy. Ms. Pasquini is rated as an Experienced expert by MediFind in the treatment of N-Acetylglutamate Synthase Deficiency. Her top areas of expertise are Short-Chain Acyl-CoA Dehydrogenase Deficiency, N-Acetylglutamate Synthase Deficiency, Homocystinuria, and Urea Cycle Disorders (UCD).
Her clinical research consists of co-authoring 21 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of N-Acetylglutamate Synthase 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.
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
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- Amyotonia CongenitaMs. Pasquini isExperienced. Learn about Amyotonia Congenita.
- HomocystinuriaMs. Pasquini isExperienced. Learn about Homocystinuria.
- Intraventricular Hemorrhage of the NewbornMs. Pasquini isExperienced. Learn about Intraventricular Hemorrhage of the Newborn.
- MELAS SyndromeMs. Pasquini isExperienced. Learn about MELAS Syndrome.
- Mucopolysaccharidoses (MPS)Ms. Pasquini isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)