Search Results - Rosanna Asselta

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  1. 1
    Factor V Deficiency

    Factor V Deficiency by Rosanna Asselta, Flora Peyvandi

    Published 2009
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  2. 2
    Inherited defects of coagulation factor V: the hemorrhagic side

    Inherited defects of coagulation factor V: the hemorrhagic side by Rosanna Asselta, Maria Luisa Tenchini, Stefano Duga

    Published 2005
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  3. 3
    Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains

    Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains by Elvezia Maria Paraboschi, Stefano Duga, Rosanna Asselta

    Published 2017
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  4. 4
    <i>ACE2</i> and <i>TMPRSS2</i> variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

    <i>ACE2</i> and <i>TMPRSS2</i> variants and expression as candidates to sex and country differences in COVID-19 severity in Italy by Rosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, Stefano Duga

    Published 2020
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  5. 5
    ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

    ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy by Rosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, Stefano Duga

    Published 2020
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  6. 6
    Genetic susceptibility to severe COVID-19

    Genetic susceptibility to severe COVID-19 by Claudio Cappadona, Valeria Rimoldi, Elvezia Maria Paraboschi, Rosanna Asselta

    Published 2023
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  7. 7
    The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis

    The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis by Giulia Cardamone, Elvezia Maria Paraboschi, Valeria Rimoldi, Stefano Duga, Giulia Soldà, Rosanna Asselta

    Published 2017
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  8. 8
    Exploring the global landscape of genetic variation in coagulation factor XI deficiency

    Exploring the global landscape of genetic variation in coagulation factor XI deficiency by Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, Marzia Menegatti, Flora Peyvandi, Ophira Salomon, Stefano Duga

    Published 2017
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  9. 9
    First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family

    First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family by Giulia Soldà, Sonia Caccia, Michela Robusto, Chiara Chiereghin, Pierangela Castorina, Umberto Ambrosetti, Stefano Duga, Rosanna Asselta

    Published 2015
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  10. 10
    A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

    A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing by Giulia Soldà, Michela Robusto, Paola Primignani, Pierangela Castorina, Elena Benzoni, Antonio Cesarani, Umberto Ambrosetti, Rosanna Asselta, Stefano Duga

    Published 2011
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  11. 11
    SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

    SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population by Luca Trotta, Ilaria Guella, Giulia Soldà, Francesca Sironi, Silvana Tesei, Margherita Canesi, Gianni Pezzoli, Stefano Goldwurm, Stefano Duga, Rosanna Asselta

    Published 2011
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  12. 12
    Glucocerebrosidase mutations in primary parkinsonism

    Glucocerebrosidase mutations in primary parkinsonism by Rosanna Asselta, Valeria Rimoldi, Chiara Siri, Roberto Cilia, Ilaria Guella, Silvana Tesei, Giulia Soldà, Gianni Pezzoli, Stefano Duga, Stefano Goldwurm

    Published 2014
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  13. 13
    Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population

    Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population by Ilaria Guella, Rosanna Asselta, Diego Ardissino, Pier Angelica Merlini, Flora Peyvandi, Sekar Kathiresan, Pier Mannuccio Mannucci, Marco Tubaro, Stefano Duga

    Published 2010
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  14. 14
    The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p

    The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p by Letizia Straniero, Valeria Rimoldi, Maura Samarani, Stefano Goldwurm, Alessio Di Fonzo, Rejko Krüger, Michela Deleidi, Massimo Aureli, Giulia Soldà, Stefano Duga, Rosanna Asselta

    Published 2017
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  15. 15
    Genetic Association and Altered Gene Expression of Mir-155 in Multiple Sclerosis Patients

    Genetic Association and Altered Gene Expression of Mir-155 in Multiple Sclerosis Patients by Elvezia Maria Paraboschi, Giulia Soldà, Donato Gemmati, Elisa Orioli, G Zeri, Maria Donata Benedetti, Alessandro Salviati, Nadia Barizzone, Maurizio Leone, Stefano Duga, Rosanna Asselta

    Published 2011
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  16. 16
    Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype

    Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombo... by Tomáš Šimurda, Monika Brunclíková, Rosanna Asselta, Sonia Caccia, Jana Žolková, Zuzana Kolková, Dušan Loderer, Ingrid Škorňová, Jan Hudeček, Zora Lasabová, Ján Staško, Peter Kubisz

    Published 2020
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  17. 17
    Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer

    Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer by Margarita Kirienko, Martina Sollini, Marinella Corbetta, Emanuele Voulaz, Noemi Gozzi, Matteo Interlenghi, Francesca Gallivanone, Isabella Castiglioni, Rosanna Asselta, Stefano Duga, Giulia Soldà, Arturo Chiti

    Published 2021
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  18. 18
    Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management

    Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Managemen... by Tomáš Šimurda, Rosanna Asselta, Jana Žolková, Monika Brunclíková, Miroslava Dobrotová, Zuzana Kolková, Dušan Loderer, Ingrid Škorňová, Jan Hudeček, Zora Lasabová, Ján Staško, Peter Kubisz

    Published 2021
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  19. 19
    Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

    Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis by Donato Gemmati, G Zeri, Elisa Orioli, Francesca E De Gaetano, Fabrizio Salvi, Ilaria Bartolomei, Sandra D’Alfonso, C. Dall’Osso, Maurizio Leone, Ajay Singh, Rosanna Asselta, Paolo Zamboni

    Published 2012
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  20. 20
    LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population

    LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population by Roberto Cilia, Chiara Siri, Damiana Rusconi, Roberta Allegra, Andrea Ghiglietti, Giorgio Sacilotto, Michela Zini, Anna Zecchinelli, Rosanna Asselta, Stefano Duga, Anna Maria Paganoni, Gianni Pezzoli, Manuela Seia, Stefano Goldwurm

    Published 2014
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