C. Soldera

A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function.

S. Marcato, A. Casonato, E. Pontara, 2004, The Journal of laboratory and clinical medicine.

An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant.

A. Bertomoro, A. Girolami, A. Casonato, 2003, Blood.

Fainting induces an acute increase in the concentration of plasma factor VIII and von Willebrand factor.

A. Bertomoro, A. Girolami, A. Casonato, 2003, Haematologica.

Effects of photobiomodulation on experimental models of peripheral nerve injury

S. Bussadori, R. Mesquita‐Ferrari, C. Soldera, 2017, Lasers in Medical Science.

An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant.

A. Bertomoro, A. Girolami, A. Casonato, 2003 .