Rezultati - Bassi, Maria Teresa

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  1. 1
    ZFYVE26/SPASTIZIN: A close link between complicated hereditary spastic paraparesis and autophagy

    ZFYVE26/SPASTIZIN: A close link between complicated hereditary spastic paraparesis and autophagy od Vantaggiato, Chiara, Clementi, Emilio, Bassi, Maria Teresa

    Izdano 2014
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  2. 2
    KIF5A and ALS2 Variants in a Family With Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis

    KIF5A and ALS2 Variants in a Family With Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis od Simone, Marta, Trabacca, Antonio, Panzeri, Elena, Losito, Luciana, Citterio, Andrea, Bassi, Maria Teresa

    Izdano 2018
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  3. 3
    The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation

    The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation od Vantaggiato, Chiara, Castelli, Marianna, Giovarelli, Matteo, Orso, Genny, Bassi, Maria Teresa, Clementi, Emilio, De Palma, Clara

    Izdano 2019
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  4. 4
    Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5

    Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5 od Romaniello, Romina, Citterio, Andrea, Panzeri, Elena, Arrigoni, Filippo, De Rinaldis, Marta, Trabacca, Antonio, Bassi, Maria Teresa

    Izdano 2021
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  5. 5
    Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP

    Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP od Buono, Roberta, Vantaggiato, Chiara, Pisa, Viviana, Azzoni, Emanuele, Bassi, Maria Teresa, Brunelli, Silvia, Sciorati, Clara, Clementi, Emilio

    Izdano 2012
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  6. 6
    Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases

    Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases od Foschi, Matteo, Vacchiano, Veria, Avoni, Patrizia, Incensi, Alex, Battaglia, Stella, Donadio, Vincenzo, Panzeri, Elena, Bassi, Maria Teresa, Liguori, Rocco, Rizzo, Giovanni

    Izdano 2019
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  7. 7
    Long‐term follow‐up in a cohort of children with isolated corpus callosum agenesis at fetal MRI

    Long‐term follow‐up in a cohort of children with isolated corpus callosum agenesis at fetal MRI od Romaniello, Romina, Arrigoni, Filippo, De Salvo, Patrizia, Bonaglia, Maria Clara, Panzeri, Elena, Bassi, Maria Teresa, Parazzini, Cecilia, Righini, Andrea, Borgatti, Renato

    Izdano 2021
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  8. 8
    SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features

    SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features od Epifanio, Roberta, Giorda, Roberto, Merlano, Maria Carolina, Zanotta, Nicoletta, Romaniello, Romina, Marelli, Susan, Russo, Silvia, Cogliati, Francesca, Bassi, Maria Teresa, Zucca, Claudio

    Izdano 2021
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  9. 9
    Syntaxin 4 Is Required for Acid Sphingomyelinase Activity and Apoptotic Function

    Syntaxin 4 Is Required for Acid Sphingomyelinase Activity and Apoptotic Function od Perrotta, Cristiana, Bizzozero, Laura, Cazzato, Denise, Morlacchi, Sara, Assi, Emma, Simbari, Fabio, Zhang, Yang, Gulbins, Erich, Bassi, Maria Teresa, Rosa, Patrizia, Clementi, Emilio

    Izdano 2010
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  10. 10
    The Low-Affinity Receptor for Neurotrophins p75(NTR) Plays a Key Role for Satellite Cell Function in Muscle Repair Acting via RhoA

    The Low-Affinity Receptor for Neurotrophins p75(NTR) Plays a Key Role for Satellite Cell Function in Muscle Repair Acting via RhoA od Deponti, Daniela, Buono, Roberta, Catanzaro, Giuseppina, De Palma, Clara, Longhi, Renato, Meneveri, Raffaella, Bresolin, Nereo, Bassi, Maria Teresa, Cossu, Giulio, Clementi, Emilio, Brunelli, Silvia

    Izdano 2009
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  11. 11
    Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes

    Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes od Velardo, Daniele, D'Angelo, Maria Grazia, Citterio, Andrea, Panzeri, Elena, Napoli, Laura, Cinnante, Claudia, Moggio, Maurizio, Comi, Giacomo Pietro, Ronchi, Dario, Bassi, Maria Teresa

    Izdano 2022
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  12. 12
    Tensor‐based morphometry using scalar and directional information of diffusion tensor MRI data (DTBM): Application to hereditary spastic paraplegia

    Tensor‐based morphometry using scalar and directional information of diffusion tensor MRI data (DTBM): Application to hereditary spastic paraplegia od Sadeghi, Neda, Arrigoni, Filippo, D'Angelo, Maria Grazia, Thomas, Cibu, Irfanoglu, M. Okan, Hutchinson, Elizabeth B., Nayak, Amritha, Modi, Pooja, Bassi, Maria Teresa, Pierpaoli, Carlo

    Izdano 2018
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  13. 13
    U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene

    U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene od Sferruzza, Giacomo, Del Bondio, Andrea, Citterio, Andrea, Vezzulli, Paolo, Guerrieri, Simone, Radaelli, Marta, Martinelli Boneschi, Filippo, Filippi, Massimo, Maltecca, Francesca, Bassi, Maria Teresa, Scarlato, Marina

    Izdano 2021
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  14. 14
    Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA

    Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA od Revenkova, Ekaterina, Focarelli, Maria Luisa, Susani, Lucia, Paulis, Marianna, Bassi, Maria Teresa, Mannini, Linda, Frattini, Annalisa, Delia, Domenico, Krantz, Ian, Vezzoni, Paolo, Jessberger, Rolf, Musio, Antonio

    Izdano 2009
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  15. 15
    Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant

    Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant od Bersano, Anna, Ranieri, Michela, Ciammola, Andrea, Cinnante, Claudia, Lanfranconi, Silvia, Dotti, Maria Teresa, Candelise, Livia, Baschirotto, Cinzia, Ghione, Isabella, Ballabio, Elena, Bresolin, Nereo, Bassi, Maria Teresa

    Izdano 2013
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  16. 16
    ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

    ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis od Vantaggiato, Chiara, Panzeri, Elena, Castelli, Marianna, Citterio, Andrea, Arnoldi, Alessia, Santorelli, Filippo Maria, Liguori, Rocco, Scarlato, Marina, Musumeci, Olimpia, Toscano, Antonio, Clementi, Emilio, Bassi, Maria Teresa

    Izdano 2018
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  17. 17
    Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism

    Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism od Zecchini, Silvia, Giovarelli, Matteo, Perrotta, Cristiana, Morisi, Federica, Touvier, Thierry, Di Renzo, Ilaria, Moscheni, Claudia, Bassi, Maria Teresa, Cervia, Davide, Sandri, Marco, Clementi, Emilio, De Palma, Clara

    Izdano 2018
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  18. 18
    Clinical and genetic features of a cohort of patients with MFN2-related neuropathy

    Clinical and genetic features of a cohort of patients with MFN2-related neuropathy od Abati, Elena, Manini, Arianna, Velardo, Daniele, Del Bo, Roberto, Napoli, Laura, Rizzo, Federica, Moggio, Maurizio, Bresolin, Nereo, Bellone, Emilia, Bassi, Maria Teresa, D’Angelo, Maria Grazia, Comi, Giacomo Pietro, Corti, Stefania

    Izdano 2022
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  19. 19
    Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders

    Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders od Romaniello, Romina, Pasca, Ludovica, Panzeri, Elena, D’Abrusco, Fulvio, Travaglini, Lorena, Serpieri, Valentina, Signorini, Sabrina, Aiello, Chiara, Bertini, Enrico, Bassi, Maria Teresa, Valente, Enza Maria, Zanni, Ginevra, Borgatti, Renato, Arrigoni, Filippo

    Izdano 2022
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  20. 20
    Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15

    Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15 od Vantaggiato, Chiara, Crimella, Claudia, Airoldi, Giovanni, Polishchuk, Roman, Bonato, Sara, Brighina, Erika, Scarlato, Marina, Musumeci, Olimpia, Toscano, Antonio, Martinuzzi, Andrea, Santorelli, Filippo Maria, Ballabio, Andrea, Bresolin, Nereo, Clementi, Emilio, Bassi, Maria Teresa

    Izdano 2013
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