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Stefano Duga

Showing results (11-20 of 141) with videos related to

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Biochimica Et Biophysica Acta|May 29, 2007
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patientManuela Platé, Rosanna Asselta, Flora Peyvandi, et al.
International Journal of Molecular Sciences|February 23, 2019
Understanding the Impact of Aberrant Splicing in Coagulation Factor V DeficiencyElvezia Maria Paraboschi, Marzia Menegatti, Flora Peyvandi, et al.
Frontiers in Genetics|January 9, 2019
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated RegionsElvezia Maria Paraboschi, Giulia Cardamone, Giulia Soldà, et al.
Thrombosis Research|May 27, 2015
Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylationRosanna Asselta, Michela Robusto, Manuela Platé, et al.
Haematologica|June 15, 2004
Rescue of activated protein C-resistance phenotype by cis-acting factor V Gly2032Asp mutationRosanna Asselta, Anna Bossone, Luigi Iannaccone, et al.
Annals of Neurology|April 8, 2010
The PDXK rs2010795 variant is not associated with Parkinson disease in ItalyIlaria Guella, Rosanna Asselta, Silvana Tesei, et al.
American Journal of Hematology|October 8, 2008
Factor XI gene mutations in factor XI deficient patients of the Czech RepublicGiancarlo Castaman, Sofia H Giacomelli, David Habart, et al.
Haematologica|June 3, 2008
Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutationsGiancarlo Castaman, Sofia H Giacomelli, Alfredo Dragani, et al.
Thrombosis and Haemostasis|May 27, 2011
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiencyIlaria Guella, Elvezia Maria Paraboschi, Willem A van Schalkwyk, et al.
Biomedicines|December 21, 2018
Genetic Association and Altered Gene Expression of <i>CYBB</i> in Multiple Sclerosis PatientsGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Pageof 15

Showing results (11-20 of 141) with videos related to

Sort By:
Pageof 15
Biochimica Et Biophysica Acta|May 29, 2007
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patientManuela Platé, Rosanna Asselta, Flora Peyvandi, et al.
International Journal of Molecular Sciences|February 23, 2019
Understanding the Impact of Aberrant Splicing in Coagulation Factor V DeficiencyElvezia Maria Paraboschi, Marzia Menegatti, Flora Peyvandi, et al.
Frontiers in Genetics|January 9, 2019
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated RegionsElvezia Maria Paraboschi, Giulia Cardamone, Giulia Soldà, et al.
Thrombosis Research|May 27, 2015
Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylationRosanna Asselta, Michela Robusto, Manuela Platé, et al.
Haematologica|June 15, 2004
Rescue of activated protein C-resistance phenotype by cis-acting factor V Gly2032Asp mutationRosanna Asselta, Anna Bossone, Luigi Iannaccone, et al.
Annals of Neurology|April 8, 2010
The PDXK rs2010795 variant is not associated with Parkinson disease in ItalyIlaria Guella, Rosanna Asselta, Silvana Tesei, et al.
American Journal of Hematology|October 8, 2008
Factor XI gene mutations in factor XI deficient patients of the Czech RepublicGiancarlo Castaman, Sofia H Giacomelli, David Habart, et al.
Haematologica|June 3, 2008
Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutationsGiancarlo Castaman, Sofia H Giacomelli, Alfredo Dragani, et al.
Thrombosis and Haemostasis|May 27, 2011
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiencyIlaria Guella, Elvezia Maria Paraboschi, Willem A van Schalkwyk, et al.
Biomedicines|December 21, 2018
Genetic Association and Altered Gene Expression of <i>CYBB</i> in Multiple Sclerosis PatientsGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Pageof 15