Overview
Massimiliano Paganelli practices in Montreal, Canada. Mr. Paganelli is rated as an Experienced expert by MediFind in the treatment of Liver Failure. His top areas of expertise are Congenital Cardiovascular Shunt, Neonatal Hemochromatosis, Cholestasis, Hepato-Pancreato-Biliary Surgery, and Liver Transplant.
His clinical research consists of co-authoring 24 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 4 articles in the study of Liver Failure.
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
- Distinguished
- Congenital Cardiovascular ShuntMr. Paganelli isDistinguished. Learn about Congenital Cardiovascular Shunt.
- Advanced
- CholestasisMr. Paganelli isAdvanced. Learn about Cholestasis.
- Neonatal HemochromatosisMr. Paganelli isAdvanced. Learn about Neonatal Hemochromatosis.
- Experienced
- Alagille SyndromeMr. Paganelli isExperienced. Learn about Alagille Syndrome.
- Bile Duct ObstructionMr. Paganelli isExperienced. Learn about Bile Duct Obstruction.
- CholangitisMr. Paganelli isExperienced. Learn about Cholangitis.
- Classic GalactosemiaMr. Paganelli isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMr. Paganelli isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Paganelli isExperienced. Learn about Galactose Epimerase Deficiency.