Stefano Duga - Dissemin

Papers authored by Stefano Duga

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2009 Silvia Spena, Rosanna Asselta, Sonia Caccia, Valeria Rimoldi, Sofia H. Giacomelli, Annarita Tagliaferri, Flora Peyvandi, Giancarlo Castaman, Stefano Duga

Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency

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Manuela Platè, Stefano Duga

, Giancarlo Castaman, Francesco Rodeghiero, Rosanna Asselta

Recurrence of the ‘deep-intronic’ FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of Veneto:

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Stefano Duga

, Ophira Salomon

Factor XI Deficiency

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This paper is made freely available by the publisher.

Ilaria Guella, Valeria Rimoldi, Rosanna Asselta, Diego Ardissino, Maura Francolini, Nicola Martinelli, Domenico Girelli, Flora Peyvandi, Marco Tubaro, Pier Angelica Merlini, Pier Mannuccio Mannucci, Stefano Duga

Association and Functional Analyses of MEF2A as a Susceptibility Gene for Premature Myocardial Infarction and Coronary Artery Disease

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Myocardial Infarction Genetics, Benjamin F. Voight, Ds Siscovick, Bf Voight, Vascular Biology Study, Nilesh J. Samani, Ja A. Spertus, Heribert Schunkert, Stephen M. Schwartz, Daniel J. Rader, Nj Samani, Muredach P. Reilly, David S. Siscovick, Heart Attack Risk, Monika Stoll and 159 other authors

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

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2008 Giancarlo Castaman, Sofia H. Giacomelli, David Habart, Rosanna Asselta, Stefano Duga

, Francesco Rodeghiero

Factor XI gene mutations in factor XI deficient patients of the Czech Republic

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Manuela Platè, Rosanna Asselta, Silvia Spena, Marta Spreafico, Sharmila Fagoonee, Flora Peyvandi, Maria Luisa Tenchini, Stefano Duga

Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion

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Claudia Dall'Osso, Ilaria Guella, Stefano Duga

, Nadia Locatelli, Elvezia Maria Paraboschi, Marta Spreafico, Abdolreza Afrasiabi, Christoph Pechlaner, Flora Peyvandi, Maria Luisa Tenchini, Rosanna Asselta

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern

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Giancarlo Castaman, Sofia H. Giacomelli, Alfredo Dragani

, Ornella Iuliani, Stefano Duga

, Francesco Rodeghiero

Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutations

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Giorgia Zadra, Rosanna Asselta, Maria Luisa Tenchini, Giancarlo Castaman, Uri Seligsohn, Pier Mannuccio Mannucci, Stefano Duga

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 Italians

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G. Castaman, S. H. Giacomelli, S. Duga

, F. Rodeghiero

Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bβ and γ chain mutations

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Ilaria Guella, Giulia Soldà, Silvia Spena, Rosanna Asselta, Rossella Ghiotto, Maria Luisa Tenchini, Giancarlo Castaman, Stefano Duga

Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect

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2007 Silvia Spena, Rosanna Asselta, Manuela Platé, Giancarlo Castaman, Stefano Duga

, Maria Luisa Tenchini

Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen ?-chain gene as a novel mechanism for congenital afibrinogenaemia

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Manuela Platé, Rosanna Asselta, Flora Peyvandi, Maria Luisa Tenchini, Stefano Duga

Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient

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R. Asselta, S. Spena, S. Duga

, M. Tenchini

Molecular Genetics of Quantitative Fibrinogen Disorders

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Luca Monaldini, Flora Peyvandi, Mehran Karimi, Massimo Malcovati, Rosanna Asselta, Maria Luisa Tenchini, Stefano Duga

Mutational screening of six afibrinogenemic patients: Identification and characterization of four novel molecular defects

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Rosanna Asselta, Marta Spreafico, Renu Saxena, Claudia Dall'Osso, Maria Luisa Tenchini, Stefano Duga

Coagulation factor V gene analysis in five Indian patients: Identification of three novel small deletions

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2006 R. Asselta, S. Duga

, M. L. Tenchini

The molecular basis of quantitative fibrinogen disorders

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Stefano Duga

Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.

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F. Peyvandi, G. Jayandharan, M. Chandy, A. Srivastava, S. M. Nakaya, M. J. Johnson, A. R. Thompson, Thompson Ar, A. Goodeve

, I. Garagiola, S. Lavoretano, M. Menegatti, R. Palla

, M. Spreafico, M. Spreaficp and 4 other authors

Genetic diagnosis of haemophilia and other inherited bleeding disorders

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Papers authored by Stefano Duga