Overview
Rossella Parini practices in Monza, Italy. Ms. Parini and is rated as an Elite expert by MediFind in the treatment of Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome). Her top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Brachydactyly Mononen Type, and Bone Marrow Transplant.
Her clinical research consists of co-authoring 113 peer reviewed articles and participating in 5 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 11 articles and participated in 1 clinical trial in the study of Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome).
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.
5 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
- Elite
- Mucopolysaccharidoses (MPS)Ms. Parini isElite. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Distinguished
- Argininosuccinic AciduriaMs. Parini isDistinguished. Learn about Argininosuccinic Aciduria.
- Brachydactyly Mononen TypeMs. Parini isDistinguished. Learn about Brachydactyly Mononen Type.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Advanced
- Acid Sphingomyelinase Deficiency (ASMD)
- Alpha MannosidosisMs. Parini isAdvanced. Learn about Alpha Mannosidosis.
- Classic GalactosemiaMs. Parini isAdvanced. Learn about Classic Galactosemia.
- Fabry DiseaseMs. Parini isAdvanced. Learn about Fabry Disease.
- Glycogen Storage Disease Type 3Ms. Parini isAdvanced. Learn about Glycogen Storage Disease Type 3.
- LipogranulomatosisMs. Parini isAdvanced. Learn about Lipogranulomatosis.
- Experienced
- Bone Marrow TransplantMs. Parini isExperienced. Learn about Bone Marrow Transplant.
- C SyndromeMs. Parini isExperienced. Learn about C Syndrome.
- CardiomyopathyMs. Parini isExperienced. Learn about Cardiomyopathy.
- ClubfootMs. Parini isExperienced. Learn about Clubfoot.
- Developmental Dysphasia FamilialMs. Parini isExperienced. Learn about Developmental Dysphasia Familial.
- DysarthriaMs. Parini isExperienced. Learn about Dysarthria.