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Grone, Brian P, Marchese, Maria, Hamling, Kyla R, Kumar, Maneesh G, Krasniak, Christopher S, Sicca, Federico, Santorelli, Filippo M, Patel, Manisha, Baraban, Scott C
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Published in PloS one (10.03.2016)
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Published in International journal of molecular sciences (13.03.2023)
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Published in Frontiers in neurology (22.01.2019)
Published in Frontiers in neurology (22.01.2019)
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Tackling Dysfunction of Mitochondrial Bioenergetics in the Brain
Zanfardino, Paola, Doccini, Stefano, Santorelli, Filippo M, Petruzzella, Vittoria
Published in International journal of molecular sciences (03.08.2021)
Published in International journal of molecular sciences (03.08.2021)
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Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysis
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Published in Neurogenetics (01.01.2018)
Published in Neurogenetics (01.01.2018)
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Ogi, Asahi, Licitra, Rosario, Naef, Valentina, Marchese, Maria, Fronte, Baldassare, Gazzano, Angelo, Santorelli, Filippo M
Published in Frontiers in veterinary science (22.01.2021)
Published in Frontiers in veterinary science (22.01.2021)
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Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking
Behne, Robert, Teinert, Julian, Wimmer, Miriam, D’Amore, Angelica, Davies, Alexandra K, Scarrott, Joseph M, Eberhardt, Kathrin, Brechmann, Barbara, Chen, Ivy Pin-Fang, Buttermore, Elizabeth D, Barrett, Lee, Dwyer, Sean, Chen, Teresa, Hirst, Jennifer, Wiesener, Antje, Segal, Devorah, Martinuzzi, Andrea, Duarte, Sofia T, Bennett, James T, Bourinaris, Thomas, Houlden, Henry, Roubertie, Agathe, Santorelli, Filippo M, Robinson, Margaret, Azzouz, Mimoun, Lipton, Jonathan O, Borner, Georg H H, Sahin, Mustafa, Ebrahimi-Fakhari, Darius
Published in Human molecular genetics (15.01.2020)
Published in Human molecular genetics (15.01.2020)
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Understanding Spreading Depression from Headache to Sudden Unexpected Death
Cozzolino, Olga, Marchese, Maria, Trovato, Francesco, Pracucci, Enrico, Ratto, Gian Michele, Buzzi, Maria Gabriella, Sicca, Federico, Santorelli, Filippo M
Published in Frontiers in neurology (01.02.2018)
Published in Frontiers in neurology (01.02.2018)
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Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice
Fortier, Manon, Cauhapé, Margaux, Buono, Suzie, Becker, Julien, Menuet, Alexia, Branchu, Julien, Ricca, Ivana, Mero, Serena, Dorgham, Karim, El Hachimi, Khalid-Hamid, Dobrenis, Kostantin, Colsch, Benoit, Samaroo, Dominic, Devaux, Morgan, Durr, Alexandra, Stevanin, Giovanni, Santorelli, Filippo M., Colombo, Sophie, Cowling, Belinda, Darios, Frédéric
Published in Neurobiology of disease (01.09.2024)
Published in Neurobiology of disease (01.09.2024)
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Branchu, Julien, Boutry, Maxime, Sourd, Laura, Depp, Marine, Leone, Céline, Corriger, Alexandrine, Vallucci, Maeva, Esteves, Typhaine, Matusiak, Raphaël, Dumont, Magali, Muriel, Marie-Paule, Santorelli, Filippo M, Brice, Alexis, El Hachimi, Khalid Hamid, Stevanin, Giovanni, Darios, Frédéric
Published in Neurobiology of disease (01.06.2017)
Published in Neurobiology of disease (01.06.2017)
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Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish model
Marchese, Maria, Bernardi, Sara, Ogi, Asahi, Licitra, Rosario, Silvi, Giada, Mero, Serena, Galatolo, Daniele, Gammaldi, Nicola, Doccini, Stefano, Ratto, Gian Michele, Rapposelli, Simona, Neuhauss, Stephan C.F., Zang, Jingjing, Rocchiccioli, Silvia, Michelucci, Elena, Ceccherini, Elisa, Santorelli, Filippo M.
Published in Neurobiology of disease (01.07.2024)
Published in Neurobiology of disease (01.07.2024)
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Cerium oxide nanoparticles: the regenerative redox machine in bioenergetic imbalance
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Published in Nanomedicine (London, England) (01.02.2017)
Published in Nanomedicine (London, England) (01.02.2017)
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Converging Role for REEP1/SPG31 in Oxidative Stress
Naef, Valentina, Meschini, Maria C, Tessa, Alessandra, Morani, Federica, Corsinovi, Debora, Ogi, Asahi, Marchese, Maria, Ori, Michela, Santorelli, Filippo M, Doccini, Stefano
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Published in International journal of molecular sciences (01.02.2023)
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Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Naef, Valentina, Marchese, Maria, Ogi, Asahi, Fichi, Gianluca, Galatolo, Daniele, Licitra, Rosario, Doccini, Stefano, Verri, Tiziano, Argenton, Francesco, Morani, Federica, Santorelli, Filippo M.
Published in International journal of molecular sciences (05.08.2021)
Published in International journal of molecular sciences (05.08.2021)
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The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15
Saffari, Afshin, Kellner, Melanie, Jordan, Catherine, Rosengarten, Helena, Mo, Alisa, Zhang, Bo, Strelko, Oleksandr, Neuser, Sonja, Davis, Marie Y, Yoshikura, Nobuaki, Futamura, Naonobu, Takeuchi, Tomoya, Nabatame, Shin, Ishiura, Hiroyuki, Tsuji, Shoji, Aldeen, Huda Shujaa, Cali, Elisa, Rocca, Clarissa, Houlden, Henry, Efthymiou, Stephanie, Assmann, Birgit, Yoon, Grace, Trombetta, Bianca A, Kivisäkk, Pia, Eichler, Florian, Nan, Haitian, Takiyama, Yoshihisa, Tessa, Alessandra, Santorelli, Filippo M, Sahin, Mustafa, Blackstone, Craig, Yang, Edward, Schüle, Rebecca, Ebrahimi-Fakhari, Darius
Published in Brain (London, England : 1878) (02.05.2023)
Published in Brain (London, England : 1878) (02.05.2023)
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Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System
Fichi, Gianluca, Naef, Valentina, Barca, Amilcare, Longo, Giovanna, Fronte, Baldassare, Verri, Tiziano, Santorelli, Filippo M, Marchese, Maria, Petruzzella, Vittoria
Published in International journal of molecular sciences (15.05.2019)
Published in International journal of molecular sciences (15.05.2019)
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Swimming in Deep Water : Zebrafish Modeling of Complicated Forms of Hereditary Spastic Paraplegia and Spastic Ataxia
Naef, Valentina, Mero, Serena, Fichi, Gianluca, D'Amore, Angelica, Ogi, Asahi, Gemignani, Federica, Santorelli, Filippo M, Marchese, Maria
Published in Frontiers in neuroscience (10.12.2019)
Published in Frontiers in neuroscience (10.12.2019)
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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype
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Published in Human molecular genetics (15.09.2014)
Published in Human molecular genetics (15.09.2014)
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