Fingerprint Dive into the research topics where Centro Cardiologico Monzino is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.

Heart Failure Medicine & Life Sciences
Atrial Fibrillation Medicine & Life Sciences
Coronary Artery Disease Medicine & Life Sciences
Therapeutics Medicine & Life Sciences
Exercise Medicine & Life Sciences
Myocardial Infarction Medicine & Life Sciences
Registries Medicine & Life Sciences
Stents Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 2018 2018

MONZINO - CARDIOCHIRURGIA, CHIRURGIA VASCOLARE E ANESTESIOLOGIA

Ricerca, U.

1/1/1812/30/18

Project: Other project

MONZINO - CARDIOLOGIA INTERVENTISTICA ED ELETTROFISIOLOGIA

Ricerca, U.

1/1/1812/30/18

Project: Other project

MONZINO - CARDIOLOGIA CRITICA E CLINICA

Ricerca, U.

1/1/1812/30/18

Project: Other project

Research Output 1968 2019

1 Citation (Scopus)

A case of right Alzheimer’s disease

Abbate, C., Trimarchi, P. D., Inglese, S., Damanti, S., Dolci, G. A. M., Ciccone, S., Rossi, P. D., Mari, D., Arosio, B. & Cesari, M., Jan 1 2019, (Accepted/In press) In : Aging clinical and experimental research.

Research output: Contribution to journalArticle

Adrenal incidentaloma: Differential diagnosis and management strategies

Morelli, V. & Palmieri, S., Mar 1 2019, In : Minerva Endocrinologica. 44, 1, p. 4-18 15 p.

Research output: Contribution to journalReview article

Differential Diagnosis
Adrenalectomy
Hydrocortisone
Randomized Controlled Trials
Hormones

A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins

Paganini, L., Hadi, L. A., Chetta, M., Rovina, D., Fontana, L., Colapietro, P., Bonaparte, E., Pezzani, L., Marchisio, P., Tabano, S. M., Costanza, J., Sirchia, S. M., Riboni, L., Milani, D. & Miozzo, M., 2019, In : Clinical Genetics. 95, 3, p. 368-374

Research output: Contribution to journalArticle

Myopia
Intellectual Disability
Exome
Genes
Phosphoadenosine Phosphosulfate