Arama Sonuçları - 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 Yazar: Vantaggiato, Chiara, Clementi, Emilio, Bassi, Maria Teresa

    Baskı/Yayın Bilgisi 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 Yazar: Simone, Marta, Trabacca, Antonio, Panzeri, Elena, Losito, Luciana, Citterio, Andrea, Bassi, Maria Teresa

    Baskı/Yayın Bilgisi 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 Yazar: Vantaggiato, Chiara, Castelli, Marianna, Giovarelli, Matteo, Orso, Genny, Bassi, Maria Teresa, Clementi, Emilio, De Palma, Clara

    Baskı/Yayın Bilgisi 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 Yazar: Romaniello, Romina, Citterio, Andrea, Panzeri, Elena, Arrigoni, Filippo, De Rinaldis, Marta, Trabacca, Antonio, Bassi, Maria Teresa

    Baskı/Yayın Bilgisi 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 Yazar: Buono, Roberta, Vantaggiato, Chiara, Pisa, Viviana, Azzoni, Emanuele, Bassi, Maria Teresa, Brunelli, Silvia, Sciorati, Clara, Clementi, Emilio

    Baskı/Yayın Bilgisi 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 Yazar: Foschi, Matteo, Vacchiano, Veria, Avoni, Patrizia, Incensi, Alex, Battaglia, Stella, Donadio, Vincenzo, Panzeri, Elena, Bassi, Maria Teresa, Liguori, Rocco, Rizzo, Giovanni

    Baskı/Yayın Bilgisi 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 Yazar: Romaniello, Romina, Arrigoni, Filippo, De Salvo, Patrizia, Bonaglia, Maria Clara, Panzeri, Elena, Bassi, Maria Teresa, Parazzini, Cecilia, Righini, Andrea, Borgatti, Renato

    Baskı/Yayın Bilgisi 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 Yazar: Epifanio, Roberta, Giorda, Roberto, Merlano, Maria Carolina, Zanotta, Nicoletta, Romaniello, Romina, Marelli, Susan, Russo, Silvia, Cogliati, Francesca, Bassi, Maria Teresa, Zucca, Claudio

    Baskı/Yayın Bilgisi 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 Yazar: Perrotta, Cristiana, Bizzozero, Laura, Cazzato, Denise, Morlacchi, Sara, Assi, Emma, Simbari, Fabio, Zhang, Yang, Gulbins, Erich, Bassi, Maria Teresa, Rosa, Patrizia, Clementi, Emilio

    Baskı/Yayın Bilgisi 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 Yazar: Deponti, Daniela, Buono, Roberta, Catanzaro, Giuseppina, De Palma, Clara, Longhi, Renato, Meneveri, Raffaella, Bresolin, Nereo, Bassi, Maria Teresa, Cossu, Giulio, Clementi, Emilio, Brunelli, Silvia

    Baskı/Yayın Bilgisi 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 Yazar: Velardo, Daniele, D'Angelo, Maria Grazia, Citterio, Andrea, Panzeri, Elena, Napoli, Laura, Cinnante, Claudia, Moggio, Maurizio, Comi, Giacomo Pietro, Ronchi, Dario, Bassi, Maria Teresa

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 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 Yazar: 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

    Baskı/Yayın Bilgisi 2013
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