Alice Bruson

Sandro Michelini 2 collaborations

Stefano Paolacci 2 collaborations

Matteo Bertelli 2 collaborations

Paolo E Maltese 1 collaboration

Maurizio Ricci 1 collaboration

Silvia Maitz 1 collaboration

Alessandro Fiorentino 1 collaboration

Roberta Serrani 1 collaboration

Alessandra Lazzerotti 1 collaboration

Sabrina Benedetti 1 collaboration

Alessandra Zulian 1 collaboration

Elena Manara 1 collaboration

Raul E Mattassi 1 collaboration

Byung-Boong Lee 1 collaboration

Bruno Amato 1 collaboration

P E Maltese 1 collaboration

E Aldanova 1 collaboration

N Kriuchkova 1 collaboration

A Averianov 1 collaboration

E Manara 1 collaboration

S Paolacci 1 collaboration

A Bruson 1 collaboration

R Miotto 1 collaboration

M Sartori 1 collaboration

G Guerri 1 collaboration

M Zuntini 1 collaboration

G Marceddu 1 collaboration

S Tezzele 1 collaboration

K Tadtaeva 1 collaboration

A Chernova 1 collaboration

N Aksyutina 1 collaboration

S Nikulina 1 collaboration

S Nodari 1 collaboration

M Bertelli 1 collaboration

Francesco Schettini 1 collaboration

Silvia Paola Corona 1 collaboration

Fabiola Giudici 1 collaboration

Carla Strina 1 collaboration

Marianna Sirico 1 collaboration

Ottavia Bernocchi 1 collaboration

Manuela Milani 1 collaboration

Nicoletta Ziglioli 1 collaboration

Sergio Aguggini 1 collaboration

Carlo Azzini 1 collaboration

Giuseppina Barbieri 1 collaboration

Valeria Cervoni 1 collaboration

Maria Rosa Cappelletti 1 collaboration

Alfredo Molteni 1 collaboration

Maria Chiara Lazzari 1 collaboration

Giuseppina Ferrero 1 collaboration

Marco Ungari 1 collaboration

Elena Marasco 1 collaboration

Luciano Xumerle 1 collaboration

Elisa Zago 1 collaboration

Davide Cerra 1 collaboration

Marco Loddo 1 collaboration

Gareth H Williams 1 collaboration

Ida Paris 1 collaboration

Giovanni Scambia 1 collaboration

Daniele Generali 1 collaboration

Affiliations

Publications (4)

Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.

Vascular anomalies: molecular bases, genetic testing and therapeutic approaches.

Putative role of Brugada syndrome genes in familial atrial fibrillation.

Clinical, Radiometabolic and Immunologic Effects of Olaparib in Locally Advanced Triple Negative Breast Cancer: The OLTRE Window of Opportunity Trial.

Réseau de co-auteurs