Resultados da pesquisa - Francesca Magri

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  1. 1
    mi<scp>RNA</scp> in spinal muscular atrophy pathogenesis and therapy

    mi<scp>RNA</scp> in spinal muscular atrophy pathogenesis and therapy Por Francesca Magri, Fiammetta Vanoli, Stefania Corti

    Publicado em 2017
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  2. 2
    SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis

    SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis Por Francesco Tafuri, Dario Ronchi, Francesca Magri, Giacomo P. Comi, Stefania Corti

    Publicado em 2015
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  3. 3
    Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy

    Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy Por Alessandra Govoni, Francesca Magri, Simona Brajkovic, Chiara Zanetta, Irene Faravelli, Stefania Corti, Nereo Bresolin, Giacomo P. Comi

    Publicado em 2013
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  4. 4
    Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies

    Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies Por Daniela Piga, Sabrina Salani, Francesca Magri, Roberta Brusa, Eleonora Mauri, Giacomo P. Comi, Nereo Bresolin, Stefania Corti

    Publicado em 2019
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  5. 5
    Gait Variability Detects Women in Early Postmenopause With Low Bone Mineral Density

    Gait Variability Detects Women in Early Postmenopause With Low Bone Mineral Density Por Kerstin M. Palombaro, Laurita M. Hack, Kathleen K Mangione, Ann E. Barr, Roberta A. Newton, Francesca Magri, Theresa Speziale

    Publicado em 2009
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  6. 6
    MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples

    MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples Por Marco Savarese, Giuseppina Di Fruscio, Margherita Mutarelli, Annalaura Torella, Francesca Magri, Filippo M. Santorelli, Giacomo P. Comi, Claudio Bruno, Vincenzo Nigro

    Publicado em 2014
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  7. 7
    New onset of alopecia areata in a patient with SARS‐CoV‐2 infection: Possible pathogenetic correlations?

    New onset of alopecia areata in a patient with SARS‐CoV‐2 infection: Possible pathogenetic correlations? Por Alfredo Rossi, Francesca Magri, Simone Michelini, Alvise Sernicola, Marta Muscianese, Gemma Caro, Marco Di Fraia, Camilla Chello, Maria Caterina Fortuna, Teresa Grieco

    Publicado em 2021
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  8. 8
    Telogen Effluvium after SARS-CoV-2 Infection: A Series of Cases and Possible Pathogenetic Mechanisms

    Telogen Effluvium after SARS-CoV-2 Infection: A Series of Cases and Possible Pathogenetic Mechanisms Por Alfredo Rossi, Francesca Magri, Alvise Sernicola, Simone Michelini, Gemma Caro, Marta Muscianese, Marco Di Fraia, Camilla Chello, Maria Caterina Fortuna, Teresa Grieco

    Publicado em 2021
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  9. 9
    Neurocognitive Profiles in Duchenne Muscular Dystrophy and Gene Mutation Site

    Neurocognitive Profiles in Duchenne Muscular Dystrophy and Gene Mutation Site Por Maria Grazia D’Angelo, Maria Luisa Lorusso, Federica Civati, Giacomo P. Comi, Francesca Magri, Roberto Del Bo, Michela Guglieri, Massimo Molteni, Anna Carla Turconi, Nereo Bresolin

    Publicado em 2011
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  10. 10
    Direct reprogramming of human astrocytes into neural stem cells and neurons

    Direct reprogramming of human astrocytes into neural stem cells and neurons Por Stefania Corti, Monica Nizzardo, Chiara Simone, Marianna Falcone, Chiara Donadoni, Sabrina Salani, Federica Rizzo, Martina Nardini, Giulietta Riboldi, Francesca Magri, Chiara Zanetta, Irene Faravelli, Nereo Bresolin, Giacomo P. Comi

    Publicado em 2012
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  11. 11
    Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy

    Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy Por Lorenzo Peverelli, Silvia Testolin, Luísa Villa, Adele D’Amico, Stefania Petrini, Chiara Favero, Francesca Magri, Lucia Morandi, Marina Mora, Tiziana Mongini, Enrico Bertini, Monica Sciacco, Giacomo P. Comi, Maurizio Moggio

    Publicado em 2015
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  12. 12
    Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies

    Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies Por Rachele Cagliani, Francesca Magri, Antonio Toscano, Luciano Merlini, Francesco Fortunato, C. Lamperti, Carmelo Rodolico, A. Prelle, Manuela Sironi, M. Aguennouz, Patrizia Ciscato, Antonino Uncini, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi

    Publicado em 2005
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  13. 13
    Genetic Correction of Human Induced Pluripotent Stem Cells from Patients with Spinal Muscular Atrophy

    Genetic Correction of Human Induced Pluripotent Stem Cells from Patients with Spinal Muscular Atrophy Por Stefania Corti, Monica Nizzardo, Chiara Simone, Marianna Falcone, Martina Nardini, Dario Ronchi, Chiara Donadoni, Sabrina Salani, Giulietta Riboldi, Francesca Magri, Giorgia Menozzi, María Clara Bonaglia, Federica Rizzo, Nereo Bresolin, Giacomo P. Comi

    Publicado em 2012
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  14. 14
    Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients

    Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients Por Francesca Magri, Roberto Del Bo, Maria Grazia D’Angelo, Monica Sciacco, S. Gandossini, Alessandra Govoni, Laura Napoli, Patrizia Ciscato, Francesco Fortunato, Erika Brighina, Sara Bonato, Andreina Bordoni, Valeria Lucchini, Stefania Corti, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi

    Publicado em 2012
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  15. 15
    Intravenous contrast ultrasound examination using contrast‐tuned imaging (CnTI™) and the contrast medium SonoVue® for discrimination between benign and malignant adnexal masses with solid components

    Intravenous contrast ultrasound examination using contrast‐tuned imaging (CnTI™) and the contrast medium SonoVue® for discrimination between benign and malignant adnexal masses wit... Por A. C. Testa, D. Timmerman, V. Van Belle, E. Fruscella, C. Van Holsbeke, L. Savelli, E. Ferrazzi, F. Leone, H. Marret, F. Tranquart, C. Exacoustòs, G. Nazzaro, Daniela Bokor, Francesca Magri, Sabine Van Huffel, Gabriella Ferrandina, L. Valentin

    Publicado em 2009
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  16. 16
    Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

    Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions Por Dario Ronchi, Caterina Garone, Andrea Bordoni, Purificación Gutiérrez Ríos, Sarah E. Calvo, Michela Ripolone, Michela Ranieri, Mafalda Rizzuti, Luísa Villa, Francesca Magri, Stefania Corti, Nereo Bresolin, Vamsi K. Mootha, M. Moggio, S. DiMauro, Giacomo P. Comi, Monica Sciacco

    Publicado em 2012
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  17. 17
    Histological effects of givinostat in boys with Duchenne muscular dystrophy

    Histological effects of givinostat in boys with Duchenne muscular dystrophy Por Paolo Bettica, Stefania Petrini, Valentina Doria, Adele D’Amico, Michela Catteruccia, Marika Pane, Serena Sivo, Francesca Magri, Simona Brajkovic, Sonia Messina, Gian Luca Vita, Barbara Gatti, Maurizio Moggio, Prem Puri, Maurizio Rocchetti, Giuseppe De Nicolao, Giuseppe Vita, Giacomo P. Comi, Enrico Bertini, Eugenio Mercuri

    Publicado em 2016
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  18. 18
    Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients

    Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients Por Irene Faravelli, Megi Meneri, Domenica Saccomanno, Daniele Velardo, Elena Abati, Delia Gagliardi, Valeria Parente, Lucia Petrozzi, Dario Ronchi, Nino Stocchetti, Edoardo Calderini, Maria Grazia D’Angelo, Giovanna Chidini, Edi Prandi, Giulia Ricci, Gabriele Siciliano, Nereo Bresolin, Giacomo P. Comi, Stefania Corti, Francesca Magri, Alessandra Govoni

    Publicado em 2020
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  19. 19
    Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability

    Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability Por Dario Ronchi, Alessio Di Fonzo, Weiqiang Lin, Andreina Bordoni, Changwei Liu, Elisa Fassone, Serena Pagliarani, Mafalda Rizzuti, Li Zheng, Massimiliano Filosto, Maria Teresa Ferrò, Michela Ranieri, Francesca Magri, Lorenzo Peverelli, Hongzhi Li, Yate‐Ching Yuan, Stefania Corti, Monica Sciacco, Maurizio Moggio, Nereo Bresolin, Binghui Shen, Giacomo P. Comi

    Publicado em 2013
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  20. 20
    Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

    Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy Por Andrea Barp, Luca Bello, Luisa Politano, Paola Melacini, Chiara Calore, Angela Polo, Sara Vianello, Gianni Sorarù, Claudio Semplicini, Boris Pantic, Antonella Taglia, Ester Picillo, Francesca Magri, Ksenija Gorni, Sonia Messina, Gian Luca Vita, Giuseppe Vita, Giacomo P. Comi, Mario Ermani, Vincenzo Calvo, C. Angelini, Eric P. Hoffman, Elena Pegoraro

    Publicado em 2015
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