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S Duga

Showing results (1-10 of 40) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|August 10, 2011
Mutations in disguiseS Duga, R Asselta
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Inherited defects of coagulation factor V: the hemorrhagic sideR Asselta, M L Tenchini, S Duga
Journal of Thrombosis and Haemostasis : JTH|September 27, 2006
The molecular basis of quantitative fibrinogen disordersR Asselta, S Duga, M L Tenchini
Journal of Thrombosis and Haemostasis : JTH|March 8, 2005
A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia VicenzaG Castaman, R Ghiotto, S Duga, et al.
Biochemical and Biophysical Research Communications|December 3, 1999
Genomic organization of the human gamma adducin geneL Citterio, T Azzani, S Duga, et al.
Cardiovascular & Hematological Agents in Medicinal Chemistry|April 14, 2007
Molecular genetics of quantitative fibrinogen disordersR Asselta, S Spena, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutationsG Castaman, S H Giacomelli, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Rare coagulation deficienciesF Peyvandi, S Duga, S Akhavan, et al.
Journal of Thrombosis and Haemostasis : JTH|September 22, 2010
Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficienciesG Castaman, M Platè, S H Giacomelli, et al.
Journal of Thrombosis and Haemostasis : JTH|October 26, 2005
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemiaL Monaldini, R Asselta, M Malcovati, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Journal of Thrombosis and Haemostasis : JTH|August 10, 2011
Mutations in disguiseS Duga, R Asselta
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Inherited defects of coagulation factor V: the hemorrhagic sideR Asselta, M L Tenchini, S Duga
Journal of Thrombosis and Haemostasis : JTH|September 27, 2006
The molecular basis of quantitative fibrinogen disordersR Asselta, S Duga, M L Tenchini
Journal of Thrombosis and Haemostasis : JTH|March 8, 2005
A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia VicenzaG Castaman, R Ghiotto, S Duga, et al.
Biochemical and Biophysical Research Communications|December 3, 1999
Genomic organization of the human gamma adducin geneL Citterio, T Azzani, S Duga, et al.
Cardiovascular & Hematological Agents in Medicinal Chemistry|April 14, 2007
Molecular genetics of quantitative fibrinogen disordersR Asselta, S Spena, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutationsG Castaman, S H Giacomelli, S Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Rare coagulation deficienciesF Peyvandi, S Duga, S Akhavan, et al.
Journal of Thrombosis and Haemostasis : JTH|September 22, 2010
Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficienciesG Castaman, M Platè, S H Giacomelli, et al.
Journal of Thrombosis and Haemostasis : JTH|October 26, 2005
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemiaL Monaldini, R Asselta, M Malcovati, et al.
Pageof 4