Hasil Pencarian - Simona Scala

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  1. 1
    Erratum to “Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson’s Disease”

    Erratum to “Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson’s Disease” oleh Stefano Gambardella, Rosangela Ferese, Simona Scala, Stefania Carboni, Francesca Biagioni, Emiliano Giardina, Stefania Zampatti, Nicola Modugno, Francesco Fabbiano, Francesco Fornai, Diego Centonze, Stefano Ruggieri

    Diterbitkan 2018-01-01
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  2. 2
    Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson’s Disease

    Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson’s Disease oleh Stefano Gambardella, Rosangela Ferese, Simona Scala, Stefania Carboni, Francesca Biagioni, Giardina Emiliano, Stefania Zampatti, Nicola Modugno, Francesco Fabbiano, Francesco Fornai, Diego Centonze, Stefano Ruggieri

    Diterbitkan 2018-01-01
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  3. 3
    MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.

    MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line. oleh Bianca Bertulat, Maria Luigia De Bonis, Floriana Della Ragione, Anne Lehmkuhl, Manuela Milden, Christian Storm, K Laurence Jost, Simona Scala, Brian Hendrich, Maurizio D'Esposito, M Cristina Cardoso

    Diterbitkan 2012-01-01
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  4. 4
    Bridging a Patient with Acute Liver Failure to Liver Transplantation by the AMC-Bioartificial Liver

    Bridging a Patient with Acute Liver Failure to Liver Transplantation by the AMC-Bioartificial Liver oleh Maarten-Paul Van De Kerkhove, Ernesto Di Florio, Vincenzo Scuderi, Antonio Mancini, Antonello Belli, Adele Bracco, Daniela Scala, Simona Scala, Laura Zeuli, Giuseppe Di Nicuolo, Pietro Amoroso, Fulvio Calise, Robert A. F. M. Chamuleau

    Diterbitkan 2003-09-01
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  5. 5
    Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease

    Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease oleh Rosangela Ferese, Simona Scala, Francesca Biagioni, Emiliano Giardina, Emiliano Giardina, Stefania Zampatti, Stefania Zampatti, Nicola Modugno, Claudio Colonnese, Claudio Colonnese, Marianna Storto, Francesco Fornai, Francesco Fornai, Giuseppe Novelli, Giuseppe Novelli, Stefano Ruggieri, Stefano Gambardella

    Diterbitkan 2018-07-01
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  6. 6
    Identification of sixteen novel candidate genes for late onset Parkinson’s disease

    Identification of sixteen novel candidate genes for late onset Parkinson’s disease oleh Alessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, Teresa Nutile, Alessia Lombardi, Luca Giovanni Di Giovannantonio, Sara Pietracupa, Daniela Ruggiero, Simona Scala, Stefano Gambardella, International Parkinson’s Disease Genomics Consortium (IPDGC), Licia Iacoviello, Fernando Gianfrancesco, Dario Acampora, Maurizio D’Esposito, Antonio Simeone, Marina Ciullo, Teresa Esposito

    Diterbitkan 2021-06-01
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  7. 7
    Cohort analysis of novel SPAST variants in SPG4 patients and implementation of in vitro and in vivo studies to identify the pathogenic mechanism caused by splicing mutations

    Cohort analysis of novel SPAST variants in SPG4 patients and implementation of in vitro and in vivo studies to identify the pathogenic mechanism caused by splicing mutations oleh Rosangela Ferese, Simona Scala, Antonio Suppa, Antonio Suppa, Rosa Campopiano, Francesco Asci, Alessandro Zampogna, Maria Antonietta Chiaravalloti, Annamaria Griguoli, Marianna Storto, Alba Di Pardo, Emiliano Giardina, Stefania Zampatti, Francesco Fornai, Francesco Fornai, Giuseppe Novelli, Giuseppe Novelli, Mirco Fanelli, Chiara Zecca, Giancarlo Logroscino, Diego Centonze, Diego Centonze, Stefano Gambardella, Stefano Gambardella

    Diterbitkan 2023-12-01
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  8. 8
    Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants

    Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants oleh Rosangela Ferese, Rosa Campopiano, Simona Scala, Carmelo D’Alessio, Marianna Storto, Fabio Buttari, Diego Centonze, Diego Centonze, Giancarlo Logroscino, Giancarlo Logroscino, Chiara Zecca, Stefania Zampatti, Stefania Zampatti, Francesco Fornai, Francesco Fornai, Vittoria Cianci, Elisabetta Manfroi, Emiliano Giardina, Emiliano Giardina, Mauro Magnani, Antonio Suppa, Antonio Suppa, Giuseppe Novelli, Giuseppe Novelli, Stefano Gambardella, Stefano Gambardella

    Diterbitkan 2021-07-01
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