Researcher
Diego Zanetti
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico Milano
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6 papers found
All papers authored by Diego Zanetti
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2021
Allan Thomas Højland 
,
Lisse J. M. Tavernier ,
Isabelle Schrauwen ,
Manou Sommen ,
Vedat Topsakal ,
Isabelle Schatteman ,
Ingeborg Dhooge ,
Alex Huber ,
Diego Zanetti ,
Henricus P. M. Kunst ,
Alexander Hoischen ,
Michael B. Petersen ,
Guy Van Camp ,
Erik Fransen
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,
Lisse J. M. Tavernier ,
Isabelle Schrauwen ,
Manou Sommen ,
Vedat Topsakal ,
Isabelle Schatteman ,
Ingeborg Dhooge ,
Alex Huber ,
Diego Zanetti ,
Henricus P. M. Kunst ,
Alexander Hoischen ,
Michael B. Petersen ,
Guy Van Camp ,
Erik Fransen
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2019
Hanne Valgaeren ,
Manou Sommen ,
Matthias Beyens ,
Geert Vandeweyer ,
Isabelle Schrauwen ,
Anne Schepers,
Isabelle Schatteman,
Vedat Topsakal ,
Ingeborg Dhooge ,
Henricus Kunst ,
Diego Zanetti ,
Alexander M. Huber ,
Alexander Hoischen ,
Erik Fransen ,
Guy Van Camp
,
Manou Sommen ,
Matthias Beyens ,
Geert Vandeweyer ,
Isabelle Schrauwen ,
Anne Schepers,
Isabelle Schatteman,
Vedat Topsakal ,
Ingeborg Dhooge ,
Henricus Kunst ,
Diego Zanetti ,
Alexander M. Huber ,
Alexander Hoischen ,
Erik Fransen ,
Guy Van Camp
Insufficient evidence for a role of SERPINF1 in otosclerosis
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2018
Lorenzo Piergallini,
Elisa Scola ,
Bruno Tuscano,
Roberto Brambilla,
Mauro Campoleoni,
Gabriella Raimondi,
Luciano Lombardi,
Federica Di Berardino ,
Diego Zanetti ,
Clara Sina,
Fabio Triulzi,
Giorgio Conte
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,
Bruno Tuscano,
Roberto Brambilla,
Mauro Campoleoni,
Gabriella Raimondi,
Luciano Lombardi,
Federica Di Berardino ,
Diego Zanetti ,
Clara Sina,
Fabio Triulzi,
Giorgio Conte
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G. Conte ,
E. Scola ,
S. Calloni ,
R. Brambilla ,
M. Campoleoni ,
L. Lombardi ,
F. Di Berardino ,
D. Zanetti ,
L. M. Gaini ,
F. Triulzi ,
C. Sina
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,
E. Scola ,
S. Calloni ,
R. Brambilla ,
M. Campoleoni ,
L. Lombardi ,
F. Di Berardino ,
D. Zanetti ,
L. M. Gaini ,
F. Triulzi ,
C. Sina
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Federica Di Berardino ,
Lennart Truedsson,
Diego Zanetti
,
Lennart Truedsson,
Diego Zanetti
Delayed Cochlear Implantation in Post-Meningitic Deafness and Hereditary Complement C2 Deficiency
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