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Stefano Duga

Showing results (1-10 of 141) with videos related to

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Seminars in Thrombosis and Hemostasis|July 15, 2009
Factor XI DeficiencyStefano Duga, Ophira Salomon
Seminars in Thrombosis and Hemostasis|August 10, 2013
Congenital factor XI deficiency: an updateStefano Duga, Ophira Salomon
Blood|May 13, 2004
Recessively inherited coagulation disordersPier Mannuccio Mannucci, Stefano Duga, Flora Peyvandi
The International Journal of Biochemistry & Cell Biology|May 19, 2004
Coagulation factor VStefano Duga, Rosanna Asselta, Maria Luisa Tenchini
International Journal of Molecular Sciences|October 27, 2020
Hereditary Hypofibrinogenemia with Hepatic StorageRosanna Asselta, Elvezia Maria Paraboschi, Stefano Duga
International Journal of Molecular Sciences|December 15, 2017
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ ChainsElvezia Maria Paraboschi, Stefano Duga, Rosanna Asselta
Frontiers in Genetics|December 28, 2020
Editorial: RNA Splicing and Backsplicing: Disease and TherapyRosanna Asselta, Stefano Duga, Eladio Andrés Velasco, et al.
Thrombosis Research|May 19, 2015
Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutationsGiancarlo Castaman, Valeria Rimoldi, Sofia H Giacomelli, et al.
Aging|June 6, 2020
<i>ACE2</i> and <i>TMPRSS2</i> variants and expression as candidates to sex and country differences in COVID-19 severity in ItalyRosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 25, 2009
Recurrence of the 'deep-intronic' FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of VenetoManuela Platè, Stefano Duga, Giancarlo Castaman, et al.
Pageof 15

Showing results (1-10 of 141) with videos related to

Sort By:
Pageof 15
Seminars in Thrombosis and Hemostasis|July 15, 2009
Factor XI DeficiencyStefano Duga, Ophira Salomon
Seminars in Thrombosis and Hemostasis|August 10, 2013
Congenital factor XI deficiency: an updateStefano Duga, Ophira Salomon
Blood|May 13, 2004
Recessively inherited coagulation disordersPier Mannuccio Mannucci, Stefano Duga, Flora Peyvandi
The International Journal of Biochemistry & Cell Biology|May 19, 2004
Coagulation factor VStefano Duga, Rosanna Asselta, Maria Luisa Tenchini
International Journal of Molecular Sciences|October 27, 2020
Hereditary Hypofibrinogenemia with Hepatic StorageRosanna Asselta, Elvezia Maria Paraboschi, Stefano Duga
International Journal of Molecular Sciences|December 15, 2017
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ ChainsElvezia Maria Paraboschi, Stefano Duga, Rosanna Asselta
Frontiers in Genetics|December 28, 2020
Editorial: RNA Splicing and Backsplicing: Disease and TherapyRosanna Asselta, Stefano Duga, Eladio Andrés Velasco, et al.
Thrombosis Research|May 19, 2015
Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutationsGiancarlo Castaman, Valeria Rimoldi, Sofia H Giacomelli, et al.
Aging|June 6, 2020
<i>ACE2</i> and <i>TMPRSS2</i> variants and expression as candidates to sex and country differences in COVID-19 severity in ItalyRosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 25, 2009
Recurrence of the 'deep-intronic' FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of VenetoManuela Platè, Stefano Duga, Giancarlo Castaman, et al.
Pageof 15