Showing 1 - 19 results of 19 for search 'Rosangela Ferese', query time: 0.05s
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ccf-mtDNA as a Potential Link Between the Brain and Immune System in Neuro-Immunological Disorders by Stefano Gambardella, Fiona Limanaqi, Rosangela Ferese, Francesca Biagioni, Rosa Campopiano, Diego Centonze, Diego Centonze, Francesco Fornai, Francesco Fornai
Published 2019-05-01
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Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson’s Disease by Alfonsina Tirozzi, Nicola Modugno, Nicole Piera Palomba, Rosangela Ferese, Alessia Lombardi, Enrica Olivola, Alessandro Gialluisi, Teresa Esposito, Teresa Esposito
Published 2021-04-01
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Occurrence of Total and Proteinase K-Resistant Alpha-Synuclein in Glioblastoma Cells Depends on mTOR Activity by Larisa Ryskalin, Rosangela Ferese, Gabriele Morucci, Francesca Biagioni, Carla L. Busceti, Fabrizio Michetti, Paola Lenzi, Alessandro Frati, Francesco Fornai
Published 2022-03-01
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A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy by Stefania Zampatti, Cristina Peconi, Giulia Calvino, Rosangela Ferese, Stefano Gambardella, Raffaella Cascella, Jacopo Sebastiani, Benedetto Falsini, Andrea Cusumano, Emiliano Giardina
Published 2023-08-01
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Quantitative Ultrastructural Morphometry and Gene Expression of mTOR-Related Mitochondriogenesis within Glioblastoma Cells by Rosangela Ferese, Paola Lenzi, Federica Fulceri, Francesca Biagioni, Cinzia Fabrizi, Stefano Gambardella, Pietro Familiari, Alessandro Frati, Fiona Limanaqi, Francesco Fornai
Published 2020-06-01
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The Autophagy-Related Organelle Autophagoproteasome Is Suppressed within Ischemic Penumbra by Francesca Biagioni, Federica Mastroiacovo, Paola Lenzi, Stefano Puglisi-Allegra, Carla L. Busceti, Larisa Ryskalin, Rosangela Ferese, Domenico Bucci, Alessandro Frati, Ferdinando Nicoletti, Francesco Fornai
Published 2021-09-01
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Autophagy Activation Associates with Suppression of Prion Protein and Improved Mitochondrial Status in Glioblastoma Cells by Paola Lenzi, Carla L. Busceti, Gloria Lazzeri, Rosangela Ferese, Francesca Biagioni, Alessandra Salvetti, Elena Pompili, Valerio De Franchis, Stefano Puglisi-Allegra, Alessandro Frati, Michela Ferrucci, Francesco Fornai
Published 2023-01-01
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Modeling native and seeded Synuclein aggregation and related cellular dysfunctions in dopaminergic neurons derived by a new set of isogenic iPSC lines with SNCA multiplications by Angelo Iannielli, Mirko Luoni, Serena Gea Giannelli, Rosangela Ferese, Gabriele Ordazzo, Matteo Fossati, Andrea Raimondi, Felipe Opazo, Olga Corti, Jochen H. M. Prehn, Stefano Gambardella, Ronald Melki, Vania Broccoli
Published 2022-10-01
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Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion by Marianna De Cinque, Marianna De Cinque, Orazio Palumbo, Ermelinda Mazzucco, Antonella Simone, Antonella Simone, Pietro Palumbo, Renata Ciavatta, Giuliana Maria, Rosangela Ferese, Stefano Gambardella, Antonella Angiolillo, Massimo Carella, Silvio Garofalo
Published 2017-12-01
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A Large Family with p.Arg554His Mutation in <i>ABCD1</i>: Clinical Features and Genotype/Phenotype Correlation in Female Carriers by Rosa Campopiano, Cinzia Femiano, Maria Antonietta Chiaravalloti, Rosangela Ferese, Diego Centonze, Fabio Buttari, Stefania Zampatti, Mirco Fanelli, Stefano Amatori, Carmelo D’Alessio, Emiliano Giardina, Francesco Fornai, Francesca Biagioni, Marianna Storto, Stefano Gambardella
Published 2021-05-01
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Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease by 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
Published 2018-07-01
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A Single Nucleotide ADA Genetic Variant Is Associated to Central Inflammation and Clinical Presentation in MS: Implications for Cladribine Treatment by Mario Stampanoni Bassi, Fabio Buttari, Ilaria Simonelli, Luana Gilio, Roberto Furlan, Annamaria Finardi, Girolama Alessandra Marfia, Andrea Visconti, Andrea Paolillo, Marianna Storto, Stefano Gambardella, Rosangela Ferese, Marco Salvetti, Antonio Uccelli, Giuseppe Matarese, Diego Centonze, Francesca De Vito
Published 2020-09-01
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Interleukin 6 SNP <i>rs1818879</i> Regulates Radiological and Inflammatory Activity in Multiple Sclerosis by Antonio Bruno, Ettore Dolcetti, Federica Azzolini, Alessandro Moscatelli, Stefano Gambardella, Rosangela Ferese, Francesca Romana Rizzo, Luana Gilio, Ennio Iezzi, Giovanni Galifi, Angela Borrelli, Fabio Buttari, Roberto Furlan, Annamaria Finardi, Francesca De Vito, Alessandra Musella, Livia Guadalupi, Georgia Mandolesi, Diego Centonze, Mario Stampanoni Bassi
Published 2022-05-01
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The BDNF Val66Met Polymorphism (rs6265) Modulates Inflammation and Neurodegeneration in the Early Phases of Multiple Sclerosis by Ettore Dolcetti, Antonio Bruno, Federica Azzolini, Luana Gilio, Alessandro Moscatelli, Francesca De Vito, Luigi Pavone, Ennio Iezzi, Stefano Gambardella, Emiliano Giardina, Rosangela Ferese, Fabio Buttari, Francesca Romana Rizzo, Roberto Furlan, Annamaria Finardi, Alessandra Musella, Georgia Mandolesi, Livia Guadalupi, Diego Centonze, Mario Stampanoni Bassi
Published 2022-02-01
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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 by 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
Published 2023-12-01
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Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants by 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
Published 2021-07-01
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Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Projec... by Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad-Annuar, Bashayer Al-Mubarak, Roy N. Alcalay, Victoria Alvarez, Ignacio Amorin, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A. Barker, Melinda Barkhuizen, A. Nazli Basak, Vincenzo Bonifati, Agnita Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimon, Mario Cornejo-Olivas, Leonor Correia Guedes, Jean-Christophe Corvol, David Crosiers, Joana Damásio, Parimal Das, Patricia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim Ferreira, Emilia Gatto, Gençer Genç, Nir Giladi, Pilar Gómez-Garre, Hasmet Hanagasi, Nobutaka Hattori, Faycal Hentati, Dorota Hoffman-Zacharska, Sergey N. Illarioshkin, Joseph Jankovic, Silvia Jesús, Valtteri Kaasinen, Anneke Kievit, Peter Klivenyi, Vladimir Kostic, Dariusz Koziorowski, Andrea A. Kühn, Anthony E. Lang, Shen-Yang Lim, Chin-Hsien Lin, Katja Lohmann, Vladana Markovic, Mika Henrik Martikainen, George Mellick, Marcelo Merello, Lukasz Milanowski, Pablo Mir, Özgür Öztop-Çakmak, Márcia Mattos Gonçalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther M. Sammler, Maria Skaalum Petersen, Matej Skorvanek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vitor Tumas, Enza Maria Valente, Bart van de Warrenburg, Caroline H. Williams-Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein
Published 2023-01-01
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Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Projec... by Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad-Annuar, Bashayer Al-Mubarak, Roy N Alcalay, Victoria Alvarez, Ignacio Amorin, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A Barker, Melinda Barkhuizen, A Nazli Basak, Vincenzo Bonifati, Agnita Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimon, Mario Cornejo-Olivas, Leonor Correia Guedes, Jean-Christophe Corvol, David Crosiers, Joana Damásio, Parimal Das, Patricia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim Ferreira, Emilia Gatto, Gençer Genç, Nir Giladi, Pilar Gómez-Garre, Hasmet Hanagasi, Nobutaka Hattori, Faycal Hentati, Dorota Hoffman-Zacharska, Sergey N Illarioshkin, Joseph Jankovic, Silvia Jesús, Valtteri Kaasinen, Anneke Kievit, Peter Klivenyi, Vladimir Kostic, Dariusz Koziorowski, Andrea A Kühn, Anthony E Lang, Shen-Yang Lim, Chin-Hsien Lin, Katja Lohmann, Vladana Markovic, Mika Henrik Martikainen, George Mellick, Marcelo Merello, Lukasz Milanowski, Pablo Mir, Özgür Öztop-Çakmak, Márcia Mattos Gonçalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther M Sammler, Maria Skaalum Petersen, Matej Skorvanek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vitor Tumas, Enza Maria Valente, Bart van de Warrenburg, Caroline H Williams-Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein
Published 2023-01-01
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