Search Results - Novara, Francesca

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  1. 1
    A Big Year for Open Access Chemistry Publishing

    A Big Year for Open Access Chemistry Publishing by Novara, Francesca Rita

    Published 2020
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  2. 2
    10 Years of Open Access Society Publishing

    10 Years of Open Access Society Publishing by Novara, Francesca Rita

    Published 2020
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  3. 3
    A Golden Ten: A Decade of Open Access Society Publishing

    A Golden Ten: A Decade of Open Access Society Publishing by Novara, Francesca Rita

    Published 2022
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  4. 4
    A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy

    A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy by Caretto, Amelia, Primerano, Liviana, Novara, Francesca, Zuffardi, Orsetta, Genovese, Stefano, Rondinelli, Maurizio

    Published 2014
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  5. 5
    MECP2 duplication phenotype in symptomatic females: report of three further cases

    MECP2 duplication phenotype in symptomatic females: report of three further cases by Novara, Francesca, Simonati, Alessandro, Sicca, Federico, Battini, Roberta, Fiori, Simona, Contaldo, Annarita, Criscuolo, Lucia, Zuffardi, Orsetta, Ciccone, Roberto

    Published 2014
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  6. 6
    Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature

    Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature by Errichiello, Edoardo, Novara, Francesca, Cremante, Anna, Verri, Annapia, Galli, Jessica, Fazzi, Elisa, Bellotti, Daniela, Losa, Laura, Cisternino, Mariangela, Zuffardi, Orsetta

    Published 2016
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  7. 7
    Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor

    Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor by Ghezzi, Daniele, Sevrioukova, Irina, Invernizzi, Federica, Lamperti, Costanza, Mora, Marina, D'Adamo, Pio, Novara, Francesca, Zuffardi, Orsetta, Uziel, Graziella, Zeviani, Massimo

    Published 2010
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  8. 8
    Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood

    Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood by Novara, Francesca, Beri, Silvana, Bernardo, Maria Ester, Bellazzi, Riccardo, Malovini, Alberto, Ciccone, Roberto, Cometa, Angela Maria, Locatelli, Franco, Giorda, Roberto, Zuffardi, Orsetta

    Published 2009
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  9. 9
    The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma

    The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma by MARTINELLI, CAROLINA, GABRIELE, FABIO, MANAI, FEDERICO, CICCONE, ROBERTO, NOVARA, FRANCESCA, SAUTA, ELISABETTA, BELLAZZI, RICCARDO, PATANE, MONICA, MORONI, ISABELLA, PATERRA, ROSINA, COMINCINI, SERGIO

    Published 2020
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  10. 10
    In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients

    In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients by Lucarelli, Enrico, Bellotti, Chiara, Mantelli, Melissa, Avanzini, Maria Antonietta, Maccario, Rita, Novara, Francesca, Arrigo, Giulia, Zuffardi, Orsetta, Zuntini, Monia, Pandolfi, Martina, Sangiorgi, Luca, Lisini, Daniela, Donati, Davide, Duchi, Serena

    Published 2014
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  11. 11
    Genome-wide copy number analysis in pediatric glioblastoma multiforme

    Genome-wide copy number analysis in pediatric glioblastoma multiforme by Giunti, Laura, Pantaleo, Marilena, Sardi, Iacopo, Provenzano, Aldesia, Magi, Alberto, Cardellicchio, Stefania, Castiglione, Francesca, Tattini, Lorenzo, Novara, Francesca, Buccoliero, Anna Maria, de Martino, Maurizio, Genitori, Lorenzo, Zuffardi, Orsetta, Giglio, Sabrina

    Published 2014
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  12. 12
    Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force

    Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force by Rinaldi, Berardo, Vaisfeld, Alessandro, Amarri, Sergio, Baldo, Chiara, Gobbi, Giuseppe, Magini, Pamela, Melli, Erto, Neri, Giovanni, Novara, Francesca, Pippucci, Tommaso, Rizzi, Romana, Soresina, Annarosa, Zampini, Laura, Zuffardi, Orsetta, Crimi, Marco

    Published 2017
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  13. 13
    MCT8 Deficiency: Extrapyramidal Symptoms and Delayed Myelination as Prominent Features

    MCT8 Deficiency: Extrapyramidal Symptoms and Delayed Myelination as Prominent Features by Tonduti, Davide, Vanderver, Adeline, Berardinelli, Angela, Schmidt, Johanna L., Collins, Christin D., Novara, Francesca, Di Genni, Antonia, Mita, Alda, Triulzi, Fabio, Brunstrom-Hernandez, Janice E., Zuffardi, Orsetta, Balottin, Umberto, Orcesi, Simona

    Published 2012
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  14. 14
    Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions

    Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions by Bonaglia, Maria C, Marelli, Susan, Novara, Francesca, Commodaro, Simona, Borgatti, Renato, Minardo, Grazia, Memo, Luigi, Mangold, Elisabeth, Beri, Silvana, Zucca, Claudio, Brambilla, Daniele, Molteni, Massimo, Giorda, Roberto, Weber, Ruthild G, Zuffardi, Orsetta

    Published 2010
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  15. 15
    Three reportedly unrelated families with Liddle’s syndrome inherited from a common ancestor

    Three reportedly unrelated families with Liddle’s syndrome inherited from a common ancestor by Pagani, Luca, Diekmann, Yoan, Sazzini, Marco, De Fanti, Sara, Rondinelli, Maurizio, Farnetti, Enrico, Casali, Bruno, Caretto, Amelia, Novara, Francesca, Zuffardi, Orsetta, Garagnani, Paolo, Mantero, Franco, Thomas, Mark G., Luiselli, Donata, Rossi, Ermanno

    Published 2017
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  16. 16
    Generation of mesenchymal stromal cells in the presence of platelet lysate: a phenotypic and functional comparison of umbilical cord blood- and bone marrow-derived progenitors

    Generation of mesenchymal stromal cells in the presence of platelet lysate: a phenotypic and functional comparison of umbilical cord blood- and bone marrow-derived progenitors by Avanzini, Maria Antonietta, Bernardo, Maria Ester, Cometa, Angela Maria, Perotti, Cesare, Zaffaroni, Nadia, Novara, Francesca, Visai, Livia, Moretta, Antonia, Del Fante, Claudia, Villa, Raffaella, Ball, Lynne M., Fibbe, Willem E., Maccario, Rita, Locatelli, Franco

    Published 2009
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  17. 17
    A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

    A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations by Conti, Valerio, Carabalona, Aurelie, Pallesi-Pocachard, Emilie, Leventer, Richard J., Schaller, Fabienne, Parrini, Elena, Deparis, Agathe A., Watrin, Françoise, Buhler, Emmanuelle, Novara, Francesca, Lise, Stefano, Pagnamenta, Alistair T., Kini, Usha, Taylor, Jenny C., Zuffardi, Orsetta, Represa, Alfonso, Keays, David Antony, Guerrini, Renzo, Falace, Antonio, Cardoso, Carlos

    Published 2017
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  18. 18
    Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases

    Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases by Novara, Francesca, Rinaldi, Berardo, Sisodiya, Sanjay M, Coppola, Antonietta, Giglio, Sabrina, Stanzial, Franco, Benedicenti, Francesco, Donaldson, Alan, Andrieux, Joris, Stapleton, Rachel, Weber, Astrid, Reho, Paolo, van Ravenswaaij-Arts, Conny, Kerstjens-Frederikse, Wilhelmina S, Vermeesch, Joris Robert, Devriendt, Koenraad, Bacino, Carlos A, Delahaye, Andrée, Maas, S M, Iolascon, Achille, Zuffardi, Orsetta

    Published 2017
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  19. 19
    Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder

    Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder by Bain, Jennifer M., Thornburg, Olivia, Pan, Cheryl, Rome-Martin, Donnielle, Boyle, Lia, Fan, Xiao, Devinsky, Orrin, Frye, Richard, Hamp, Silke, Keator, Cynthia G., LaMarca, Nicole M., Maddocks, Alexis B.R., Madruga-Garrido, Marcos, Niederhoffer, Karen Y., Novara, Francesca, Peron, Angela, Poole-Di Salvo, Elizabeth, Salazar, Rachel, Skinner, Steven A., Soares, Gabriela, Goldman, Sylvie, Chung, Wendy K.

    Published 2021
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  20. 20
    A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

    A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures by Sharp, Andrew J, Mefford, Heather C, Li, Kelly, Baker, Carl, Skinner, Cindy, Stevenson, Roger E, Schroer, Richard J, Novara, Francesca, De Gregori, Manuela, Ciccone, Roberto, Broomer, Adam, Casuga, Iris, Wang, Yu, Xiao, Chunlin, Barbacioru, Catalin, Gimelli, Giorgio, Bernardina, Bernardo Dalla, Torniero, Claudia, Giorda, Roberto, Regan, Regina, Murday, Victoria, Mansour, Sahar, Fichera, Marco, Castiglia, Lucia, Failla, Pinella, Ventura, Mario, Jiang, Zhaoshi, Cooper, Gregory M, Knight, Samantha JL, Romano, Corrado, Zuffardi, Orsetta, Chen, Caifu, Schwartz, Charles E, Eichler, Evan E

    Published 2008
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