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Alessandro Simonati

Showing results (41-50 of 76) with videos related to

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Developmental Medicine and Child Neurology|May 26, 2017
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5Alessandro Simonati, Ruth E Williams, Nardo Nardocci, et al.
Autism Research : Official Journal of the International Society for Autism Research|November 6, 2023
Risk of psychosis in autism spectrum disorder individuals exposed to psychosocial stressors: A 9-year chart review studyRiccardo Bortoletto, Lorenzo Bassani, Marco Garzitto, et al.
Neurology|October 3, 2014
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs diseaseRoberto Di Fabio, Francesca Moro, Liliana Pestillo, et al.
Frontiers in Molecular Neuroscience|September 8, 2017
The Networks of Genes Encoding Palmitoylated Proteins in Axonal and Synaptic Compartments Are Affected in PPT1 Overexpressing Neuronal-Like CellsFrancesco Pezzini, Marzia Bianchi, Salvatore Benfatto, et al.
Clinical Dysmorphology|October 4, 2023
Long-term outcome of a cohort of Italian patients affected with alpha-MannosidosisAnna Bertolini, Miriam Rigoldi, Annalia Cianflone, et al.
Neuromolecular Medicine|December 29, 2015
Proteomic Profiling in the Brain of CLN1 Disease Model Reveals Affected Functional ModulesSaara Tikka, Evanthia Monogioudi, Athanasios Gotsopoulos, et al.
Journal of the Neurological Sciences|September 15, 2009
Friedreich's ataxia: oxidative stress and cytoskeletal abnormalitiesMarco Sparaco, Laura Maria Gaeta, Filippo Maria Santorelli, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Neurogenetics|November 26, 2008
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing lossAlessandra Terracciano, Carlo Casali, Gaetano S Grieco, et al.
Neurogenetics|February 10, 2018
Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature reviewFrancesco Mari, Beatrice Berti, Alessandro Romano, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Developmental Medicine and Child Neurology|May 26, 2017
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5Alessandro Simonati, Ruth E Williams, Nardo Nardocci, et al.
Autism Research : Official Journal of the International Society for Autism Research|November 6, 2023
Risk of psychosis in autism spectrum disorder individuals exposed to psychosocial stressors: A 9-year chart review studyRiccardo Bortoletto, Lorenzo Bassani, Marco Garzitto, et al.
Neurology|October 3, 2014
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs diseaseRoberto Di Fabio, Francesca Moro, Liliana Pestillo, et al.
Frontiers in Molecular Neuroscience|September 8, 2017
The Networks of Genes Encoding Palmitoylated Proteins in Axonal and Synaptic Compartments Are Affected in PPT1 Overexpressing Neuronal-Like CellsFrancesco Pezzini, Marzia Bianchi, Salvatore Benfatto, et al.
Clinical Dysmorphology|October 4, 2023
Long-term outcome of a cohort of Italian patients affected with alpha-MannosidosisAnna Bertolini, Miriam Rigoldi, Annalia Cianflone, et al.
Neuromolecular Medicine|December 29, 2015
Proteomic Profiling in the Brain of CLN1 Disease Model Reveals Affected Functional ModulesSaara Tikka, Evanthia Monogioudi, Athanasios Gotsopoulos, et al.
Journal of the Neurological Sciences|September 15, 2009
Friedreich's ataxia: oxidative stress and cytoskeletal abnormalitiesMarco Sparaco, Laura Maria Gaeta, Filippo Maria Santorelli, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Neurogenetics|November 26, 2008
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing lossAlessandra Terracciano, Carlo Casali, Gaetano S Grieco, et al.
Neurogenetics|February 10, 2018
Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature reviewFrancesco Mari, Beatrice Berti, Alessandro Romano, et al.
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