Search Results - BETTINAGLIO, Paola

  • Showing 1 - 10 results of 10
Refine Results
  1. 1
    Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

    Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome by Caprioli, Jessica, Noris, Marina, Brioschi, Simona, Pianetti, Gaia, Castelletti, Federica, Bettinaglio, Paola, Mele, Caterina, Bresin, Elena, Cassis, Linda, Gamba, Sara, Porrati, Francesca, Bucchioni, Sara, Monteferrante, Giuseppe, Fang, Celia J., Liszewski, M.K., Kavanagh, David, Atkinson, John P., Remuzzi, Giuseppe

    Published in Blood
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Angiotensin Converting Enzyme Insertion/Deletion Polymorphism and Renoprotection in Diabetic and Nondiabetic Nephropathies

    Angiotensin Converting Enzyme Insertion/Deletion Polymorphism and Renoprotection in Diabetic and Nondiabetic Nephropathies by Ruggenenti, Piero, Bettinaglio, Paola, Pinares, Franck, Remuzzi, Giuseppe

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Expression analysis of NF1‐mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR

    Expression analysis of NF1‐mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR by Bettinaglio, Paola, Tritto, Viviana, Paterra, Rosina, Eoli, Marica, Riva, Paola

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  4. 4
    Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes

    Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes by Tritto, Viviana, Bettinaglio, Paola, Mangano, Eleonora, Cesaretti, Claudia, Marasca, Federica, Castronovo, Chiara, Bordoni, Roberta, Battaglia, Cristina, Saletti, Veronica, Ranzani, Valeria, Bodega, Beatrice, Eoli, Marica, Natacci, Federica, Riva, Paola

    Published in Human genetics
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  5. 5
    New insights into the molecular basis of spinal neurofibromatosis type 1

    New insights into the molecular basis of spinal neurofibromatosis type 1 by Bettinaglio, Paola, Mangano, Eleonora, Tritto, Viviana, Bordoni, Roberta, Paterra, Rosina, Borghi, Arianna, Volontè, Marinella, Battaglia, Cristina, Saletti, Veronica, Cesaretti, Claudia, Natacci, Federica, Melone, Mariarosa A B, Eoli, Marica, Riva, Paola

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort

    A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort by Paterra, Rosina, Bettinaglio, Paola, Borghi, Arianna, Mangano, Eleonora, Tritto, Viviana, Cesaretti, Claudia, Schettino, Carla, Bordoni, Roberta, Santoro, Claudia, Avignone, Sabrina, Moscatelli, Marco, Melone, Mariarosa Anna Beatrice, Saletti, Veronica, Piluso, Giulio, Natacci, Federica, Riva, Paola, Eoli, Marica

    Published in Cancers
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    BIOM-10. PREVALENCE OF NF1 MISSENSE MUTATIONS AND CANDIDATE MODIFIER GENES IN SPINAL NEUROFIBROMATOSIS PATIENTS

    BIOM-10. PREVALENCE OF NF1 MISSENSE MUTATIONS AND CANDIDATE MODIFIER GENES IN SPINAL NEUROFIBROMATOSIS PATIENTS by Riva, Paola, Bianchessi, Donata, Mangano, Eleonora, Cesaretti, Claudia, Bettinaglio, Paola, Bordoni, Roberta, Tritto, Viviana, Battaglia, Cristina, Cagnoli, Giulia, Saletti, Veronica, Melone, Marina, Schettino, Carla, Natacci, Federica, Finocchiaro, Gaetano, Eoli, Marica

    Get full text
    Article
    Save to List
    Saved in:
  8. 8
    Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

    Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease by Caprioli, Jessica, Castelletti, Federica, Bucchioni, Sara, Bettinaglio, Paola, Bresin, Elena, Pianetti, Gaia, Gamba, Sara, Brioschi, Simona, Daina, Erica, Remuzzi, Giuseppe, Noris, Marina

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  9. 9
    The molecular basis of Familial hemolytic uremic syndrome : Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20

    The molecular basis of Familial hemolytic uremic syndrome : Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20 by CAPRIOLI, Jessica, BETTINAGLIO, Paola, ZIPFEL, Peter F, AMADEI, Barbara, DAINA, Erica, GAMBA, Sara, SKERKA, Christine, MARZILIANO, Nicola, REMUZZI, Giuseppe, NORIS, Marina

    Get full text
    Article
    Save to List
    Saved in:
  10. 10
    Single strand conformation polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene

    Single strand conformation polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene by Bettinaglio, Paola, Galbusera, Andrea, Caprioli, Jessica, Orisio, Silvia, Perna, Annalisa, Arnoldi, Federica, Bucchioni, Sara, Noris, Marina

    Published in Clinical biochemistry
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: