Search Results - Veniani, Emanuela

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  1. 1
    Clinical evaluation and molecular screening of a large consecutive series of albino patients

    Clinical evaluation and molecular screening of a large consecutive series of albino patients by Mauri, Lucia, Manfredini, Emanuela, Del Longo, Alessandra, Veniani, Emanuela, Scarcello, Manuela, Terrana, Roberta, Radaelli, Adriano Egidio, Calò, Donata, Mingoia, Giuseppe, Rossetti, Antonella, Marsico, Giovanni, Mazza, Marco, Gesu, Giovanni Pietro, Cristina Patrosso, Maria, Penco, Silvana, Piozzi, Elena, Primignani, Paola

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  2. 2
    Detection of the first OCA6 Italian patient in a large cohort of albino subjects

    Detection of the first OCA6 Italian patient in a large cohort of albino subjects by Veniani, Emanuela, Mauri, Lucia, Manfredini, Emanuela, Gesu, Giovanni P, Patrosso, Maria Cristina, Zelante, Leopoldo, D’Agruma, Leonardo, Del Longo, Alessandra, Mazza, Marco, Piozzi, Elena, Penco, Silvana, Primignani, Paola

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  3. 3
    Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1 , IDH2 , and TERT mutation status

    Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1 , IDH2 , and TERT mutation status by Pesenti, Chiara, Paganini, Leda, Fontana, Laura, Veniani, Emanuela, Runza, Letterio, Ferrero, Stefano, Bosari, Silvano, Menghi, Maura, Marfia, Giovanni, Caroli, Manuela, Silipigni, Rosamaria, Guerneri, Silvana, Tabano, Silvia, Miozzo, Monica

    Published in Oncotarget
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  4. 4
    A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report

    A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report by Cennamo, Michele, Sirocchi, Davide, Giudici, Carolina, Giagnacovo, Marzia, Petracco, Guido, Ferrario, Daniela, Garganigo, Simona, Papa, Angela, Veniani, Emanuela, Squizzato, Alessandro, Del Vecchio, Lucia, Patriarca, Carlo, Partenope, Michelarcangelo, Modena, Piergiorgio

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  5. 5
    Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations

    Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations by Primignani, Paola, Allegrini, Davide, Manfredini, Emanuela, Romitti, Lorenza, Mauri, Lucia, Patrosso, Maria Cristina, Veniani, Emanuela, Franzoni, Alessandra, Del Longo, Alessandra, Gesu, Giovanni Pietro, Piozzi, Elena, Damante, Giuseppe, Penco, Silvana

    Published in Ophthalmic genetics
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  6. 6
    A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report

    A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report by Cennamo, Michele, Sirocchi, Davide, Giudici, Carolina, Giagnacovo, Marzia, Petracco, Guido, Ferrario, Daniela, Garganigo, Simona, Papa, Angela, Veniani, Emanuela, Squizzato, Alessandro, Del Vecchio, Lucia, Patriarca, Carlo, Partenope, Michelarcangelo, Modena, Piergiorgio

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  7. 7
    Detection of the first OCA6 Italian patient in a large cohort of albino subjects

    Detection of the first OCA6 Italian patient in a large cohort of albino subjects by Veniani, Emanuela, Mauri, Lucia, Manfredini, Emanuela, Gesu, Giovanni P, Patrosso, Maria Cristina, Zelante, Leopoldo, D'Agruma, Leonardo, Del Longo, Alessandra, Mazza, Marco, Piozzi, Elena, Penco, Silvana, Primignani, Paola

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  8. 8
    Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations

    Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations by Primignani, Paola, Allegrini, Davide, Manfredini, Emanuela, Romitti, Lorenza, Mauri, Lucia, Patrosso, Maria Cristina, Veniani, Emanuela, Franzoni, Alessandra, Del Longo, Alessandra, Gesu, Giovanni Pietro, Piozzi, Elena, Damante, Giuseppe, Penco, Silvana

    Published in Ophthalmic Genetics
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