Ngā hua rapu - Rosanna Asselta

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  1. 1
    Factor V Deficiency

    Factor V Deficiency mā Rosanna Asselta, Flora Peyvandi

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Revisão
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  2. 2
    Inherited defects of coagulation factor V: the hemorrhagic side

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

    I whakaputaina 2005
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā Elvezia Maria Paraboschi, Stefano Duga, Rosanna Asselta

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Rosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, Stefano Duga

    I whakaputaina 2020
    Whiwhi kuputuhi katoa
    Pré-impressão
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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 mā Rosanna Asselta, Elvezia Maria Paraboschi, Alberto Mantovani, Stefano Duga

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Genetic susceptibility to severe COVID-19

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

    I whakaputaina 2023
    Whiwhi kuputuhi katoa
    Revisão
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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 mā Giulia Cardamone, Elvezia Maria Paraboschi, Valeria Rimoldi, Stefano Duga, Giulia Soldà, Rosanna Asselta

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, Marzia Menegatti, Flora Peyvandi, Ophira Salomon, Stefano Duga

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Giulia Soldà, Sonia Caccia, Michela Robusto, Chiara Chiereghin, Pierangela Castorina, Umberto Ambrosetti, Stefano Duga, Rosanna Asselta

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Giulia Soldà, Michela Robusto, Paola Primignani, Pierangela Castorina, Elena Benzoni, Antonio Cesarani, Umberto Ambrosetti, Rosanna Asselta, Stefano Duga

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Luca Trotta, Ilaria Guella, Giulia Soldà, Francesca Sironi, Silvana Tesei, Margherita Canesi, Gianni Pezzoli, Stefano Goldwurm, Stefano Duga, Rosanna Asselta

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Glucocerebrosidase mutations in primary parkinsonism

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

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Ilaria Guella, Rosanna Asselta, Diego Ardissino, Pier Angelica Merlini, Flora Peyvandi, Sekar Kathiresan, Pier Mannuccio Mannucci, Marco Tubaro, Stefano Duga

    I whakaputaina 2010
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Letizia Straniero, Valeria Rimoldi, Maura Samarani, Stefano Goldwurm, Alessio Di Fonzo, Rejko Krüger, Michela Deleidi, Massimo Aureli, Giulia Soldà, Stefano Duga, Rosanna Asselta

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Elvezia Maria Paraboschi, Giulia Soldà, Donato Gemmati, Elisa Orioli, G Zeri, Maria Donata Benedetti, Alessandro Salviati, Nadia Barizzone, Maurizio Leone, Stefano Duga, Rosanna Asselta

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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... mā Tomáš Šimurda, Monika Brunclíková, Rosanna Asselta, Sonia Caccia, Jana Žolková, Zuzana Kolková, Dušan Loderer, Ingrid Škorňová, Jan Hudeček, Zora Lasabová, Ján Staško, Peter Kubisz

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā Margarita Kirienko, Martina Sollini, Marinella Corbetta, Emanuele Voulaz, Noemi Gozzi, Matteo Interlenghi, Francesca Gallivanone, Isabella Castiglioni, Rosanna Asselta, Stefano Duga, Giulia Soldà, Arturo Chiti

    I whakaputaina 2021
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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... mā Tomáš Šimurda, Rosanna Asselta, Jana Žolková, Monika Brunclíková, Miroslava Dobrotová, Zuzana Kolková, Dušan Loderer, Ingrid Škorňová, Jan Hudeček, Zora Lasabová, Ján Staško, Peter Kubisz

    I whakaputaina 2021
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā 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

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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