Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Giovanna Zorzi"'
Autor:
Enrica Zanuttigh, Ejona Rusha, Camille Peron, Dario Brunetti, Giovanna Zorzi, Anna Pertek, Polyxeni Nteli, Juliane Winkelmann, Valeria Tiranti, Arcangela Iuso
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103197- (2023)
Mitochondrial membrane Protein-Associated Neurodegeneration (MPAN) is a lethal neurodegenerative disorder caused by mutations in the human gene C19orf12. The molecular mechanisms underlying the disorder are still unclear, and no established therapy i
Externí odkaz:
https://doaj.org/article/8d4057d7cd0f4a128c2f6048a79d7279
Autor:
Claudia Casellato, Emilia Ambrosini, Andrea Galbiati, Emilia Biffi, Ambra Cesareo, Elena Beretta, Francesca Lunardini, Giovanna Zorzi, Terence D. Sanger, Alessandra Pedrocchi
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 16, Iss 1, Pp 1-14 (2019)
Abstract Background This study is aimed at better understanding the role of a wearable and silent ElectroMyoGraphy-based biofeedback on motor learning in children and adolescents with primary and secondary dystonia. Methods A crossover study with a w
Externí odkaz:
https://doaj.org/article/ce12c20191c1474ea4b5ea32addf4a1f
Autor:
Federica Rachele Danti, Federica Invernizzi, Isabella Moroni, Barbara Garavaglia, Nardo Nardocci, Giovanna Zorzi
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Paroxysmal exercise-induced neurological symptoms (PENS) encompass a wide spectrum of clinical phenomena commonly presenting during childhood and characteristically elicited by physical exercise. Interestingly, few shared pathogenetic mechanisms have
Externí odkaz:
https://doaj.org/article/ab32dcdb82414658b62c83c1f0f921f8
Autor:
Marco Moscatelli, Anna Ardissone, Eleonora Lamantea, Giovanna Zorzi, Claudio Bruno, Isabella Moroni, Alessandra Erbetta, Luisa Chiapparini
Publikováno v:
Neurological Sciences. 43:2081-2084
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::177ef9fe6a1b1a933751e7ce537a8d18
https://doi.org/10.1007/s10072-022-05881-8
https://doi.org/10.1007/s10072-022-05881-8
Autor:
Daniëlle G. M. Bosch, Nicole Corsten-Janssen, Colin A Ellis, Dirk Lefeber, Alfredo Brusco, Irene Bagnasco, Andrea Accogli, Ellen Macnamara, Carlo Di Bonaventura, Giovanna Zorzi, Scott Demarest, Erik A. Eklund, Noëlle Mercier, Carlo Marcelis, Rong Zhang, Ban H Edani, Camilo Toro, Ziv Gan-Or, Simone Pizzi, Kariona A. Grabińska, Nienke E. Verbeek, Karen W. Gripp, Simone Martinelli, Caterina Caputi, Luca Pannone, Marco Tartaglia, Felix Distelmaier, Louise Amlie-Wolf, Luisa Averdunk, Anne-Sophie Alaix, Renzo Guerrini, Laura Masuelli, Marwan Shinawi, Sunita Venkateswaran, Joseph Peeden, Hana Hansikova, Lucie Zdrazilova, William C. Sessa, Serena Galosi, Renske Oegema, Patricia G Wheeler, Kristin W. Barañano, Vincenzo Leuzzi, Frances Elmslie, Fadi F. Hamdan, Roberto Bei, Jean-Marc Good, Isis Atallah, Myriam Srour, Erik-Jan Kamsteeg
Publikováno v:
Brain, 145, 1, pp. 208-223
Brain
Brain, 145(1), 208-223. Oxford University Press
Brain, vol. 145, no. 1, pp. 208-223
Brain, 145, 208-223
Brain
Brain, 145(1), 208-223. Oxford University Press
Brain, vol. 145, no. 1, pp. 208-223
Brain, 145, 208-223
Subcellular membrane systems are highly enriched in dolichol, whose role in organelle homeostasis and endosomal-lysosomal pathway remains largely unclear besides being involved in protein glycosylation. DHDDS encodes for the catalytic subunit (DHDDS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012cb40531119a7d00e4415b8540c52c
https://research.rug.nl/en/publications/50de5bd9-24f7-4573-b0f2-fed69db9588d
https://research.rug.nl/en/publications/50de5bd9-24f7-4573-b0f2-fed69db9588d
Autor:
Alessia Nasca, Niccolò E Mencacci, Federica Invernizzi, Michael Zech, Ignacio J Keller Sarmiento, Andrea Legati, Chiara Frascarelli, Bernabe I Bustos, Luigi M Romito, Dimitri Krainc, Juliane Winkelmann, Miryam Carecchio, Nardo Nardocci, Giovanna Zorzi, Holger Prokisch, Steven J Lubbe, Barbara Garavaglia, Daniele Ghezzi
ATP5F1B is a subunit of the mitochondrial ATP synthase or complex V of the mitochondrial respiratory chain. Pathogenic variants in nuclear genes encoding assembly factors or structural subunits are associated with complex V deficiency, typically char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acc0a70a573e994c73106c4c132d31db
https://hdl.handle.net/11577/3470500
https://hdl.handle.net/11577/3470500
Autor:
Giovanna Zorzi, Luisa Chiapparini
Publikováno v:
AJNR. American journal of neuroradiology. 43(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a9a47bb363b06500b7023bc6577502
https://pubmed.ncbi.nlm.nih.gov/36396333
https://pubmed.ncbi.nlm.nih.gov/36396333
Autor:
Maria Novelli, Serena Galosi, Giovanna Zorzi, Simone Martinelli, Alessandro Capuano, Francesca Nardecchia, Tiziana Granata, Luca Pollini, Martina Di Rocco, Carlo Efisio Marras, Nardo Nardocci, Vincenzo Leuzzi
Publikováno v:
Parkinsonism & Related Disorders. :105405
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49d79e8a80d3a2dd1bbf632c0843a86f
https://doi.org/10.1016/j.parkreldis.2023.105405
https://doi.org/10.1016/j.parkreldis.2023.105405
Autor:
Vincenzo Levi, Ivano Dones, Luigi Romito, Angelo Franzini, Irene Tramacere, Giuseppe Messina, Giovanna Zorzi, Nardo Nardocci
Publikováno v:
Journal of Neurosurgery. 134:197-207
OBJECTIVEFirst-line pharmacological therapies have shown limited efficacy in status dystonicus (SD), while surgery is increasingly reported as remediable in refractory cases. In this context, there is no evidence regarding which neurosurgical approac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::051956bb32436ad62621c12baf8c92c9
https://doi.org/10.3171/2019.10.jns191691
https://doi.org/10.3171/2019.10.jns191691
Autor:
Manju A. Kurian, Joanna M. Flowers, Kishore R. Kumar, Glenn Anderson, Sniya Sudhakar, Matej Skorvanek, Bernhard Haslinger, Kshitij Mankad, Martje E. van Egmond, Corien Verschuuren, Rauan Kaiyrzhanov, Nicholas W. Wood, Arianna Ferrini, Nardo Nardocci, Riccardo Berutti, Arcangela Iuso, Barbara Plecko, Juliane Winkelmann, Matias Wagner, P. Darveniza, Philippe Coubes, Arianna Tucci, Paulina Gonzalez-Latapi, Ryan L. Davis, Diane Demailly, Katy Barwick, Erik-Jan Kamsteeg, Kai Bötzel, Tomasz Kmieć, Ján Necpál, Giovanna Zorzi, Derek Burke, Sylvia Boesch, Dora Steel, Barbara Garavaglia, Steven J. Lubbe, Bernabé I. Bustos, Carolyn M. Sue, Chen Zhao, Meriel McEntagart, Stephen Tisch, Henry Houlden, Jan C. Koch, Robert Jech, Sarah Wiethoff, Michael Zech, Laura Cif, Niccolo E. Mencacci, Marina A. J. Tijssen, Suvasini Sharma, Kathryn J. Peall, Paul Gissen, Kathleen M. Gorman
Publikováno v:
Annals of Neurology. 88:867-877
Objectives The majority of people with suspected genetic dystonia remain undiagnosed after maximal investigation, implying that a number of causative genes have not yet been recognised. We aimed to investigate this paucity of diagnoses. Methods We un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c14c3cabef77353a5d7d2e0a2e0c50f
https://doi.org/10.1002/ana.25879
https://doi.org/10.1002/ana.25879