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Stefano Duga

Showing results (31-40 of 141) with videos related to

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Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Parkinsonism & Related Disorders|September 28, 2020
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variantsLetizia Straniero, Valeria Rimoldi, Giada Melistaccio, et al.
Haematologica|May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain geneLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
Blood|June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiencyRosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
European Journal of Human Genetics : EJHG|October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Haematologica|April 5, 2008
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient ItaliansGiorgia Zadra, Rosanna Asselta, Maria Luisa Tenchini, et al.
Thrombosis and Haemostasis|September 9, 2011
Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian populationIlaria Guella, Stefano Duga, Diego Ardissino, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Pageof 15

Showing results (31-40 of 141) with videos related to

Sort By:
Pageof 15
Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Parkinsonism & Related Disorders|September 28, 2020
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variantsLetizia Straniero, Valeria Rimoldi, Giada Melistaccio, et al.
Haematologica|May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain geneLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
Blood|June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiencyRosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
European Journal of Human Genetics : EJHG|October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Haematologica|April 5, 2008
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient ItaliansGiorgia Zadra, Rosanna Asselta, Maria Luisa Tenchini, et al.
Thrombosis and Haemostasis|September 9, 2011
Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian populationIlaria Guella, Stefano Duga, Diego Ardissino, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Pageof 15