Zobrazeno 1 - 10
of 573
pro vyhledávání: '"Di Pardo A"'
Autor:
Noro, Fabrizia, Pepe, Giuseppe, Pizzati, Ludovica, Di Pardo, Alba, Donati, Maria Benedetta, de Gaetano, Giovanni, Iacoviello, Licia, Maglione, Vittorio, Cerletti, Chiara
Publikováno v:
In Journal of Thrombosis and Haemostasis November 2024 22(11):3221-3234
Autor:
Pepe, Giuseppe, Cotugno, Maria, Marracino, Federico, Capocci, Luca, Pizzati, Ludovica, Forte, Maurizio, Stanzione, Rosita, Scarselli, Pamela, Di Pardo, Alba, Sciarretta, Sebastiano, Volpe, Massimo, Rubattu, Speranza, Maglione, Vittorio
Publikováno v:
In BBA - Molecular and Cell Biology of Lipids January 2024 1869(1)
Autor:
Giorgia Maria Ferlazzo, Anna Maria Gambetta, Sonia Amato, Noemi Cannizzaro, Silvia Angiolillo, Mattia Arboit, Linda Diamante, Elena Carbognin, Patrizia Romani, Federico La Torre, Elena Galimberti, Florian Pflug, Mirko Luoni, Serena Giannelli, Giuseppe Pepe, Luca Capocci, Alba Di Pardo, Paola Vanzani, Lucio Zennaro, Vania Broccoli, Martin Leeb, Enrico Moro, Vittorio Maglione, Graziano Martello
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-24 (2023)
Abstract Huntington’s disease (HD) is a neurodegenerative disorder caused by CAG-repeat expansions in the huntingtin (HTT) gene. The resulting mutant HTT (mHTT) protein induces toxicity and cell death via multiple mechanisms and no effective therap
Externí odkaz:
https://doaj.org/article/c1ac1fcec269480f96fa0a3e4fd588a3
Autor:
Rosangela Ferese, Simona Scala, Antonio Suppa, Rosa Campopiano, Francesco Asci, Alessandro Zampogna, Maria Antonietta Chiaravalloti, Annamaria Griguoli, Marianna Storto, Alba Di Pardo, Emiliano Giardina, Stefania Zampatti, Francesco Fornai, Giuseppe Novelli, Mirco Fanelli, Chiara Zecca, Giancarlo Logroscino, Diego Centonze, Stefano Gambardella
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionPure hereditary spastic paraplegia (SPG) type 4 (SPG4) is caused by mutations of SPAST gene. This study aimed to analyze SPAST variants in SPG4 patients to highlight the occurrence of splicing mutations and combine functional studies to a
Externí odkaz:
https://doaj.org/article/cd13a9fba9c44771b550bdb4a169ec6c
Autor:
Johannes Burtscher, Barbara Strasser, Giuseppe Pepe, Martin Burtscher, Martin Kopp, Alba Di Pardo, Vittorio Maglione, Andy V. Khamoui
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 9, p 4696 (2024)
Prominent pathological features of Huntington’s disease (HD) are aggregations of mutated Huntingtin protein (mHtt) in the brain and neurodegeneration, which causes characteristic motor (such as chorea and dystonia) and non-motor symptoms. However,
Externí odkaz:
https://doaj.org/article/fa664a9535894977a22ac1a6be20f4ae
Autor:
Alessandra Sborgia, Giacomo Boscia, Alfredo Niro, Luca Landini, Valentina Pastore, Valeria Albano, Marina Piepoli, Rossella Donghia, Stefano Dore, Pasquale Viggiano, Rosa Buonamassa, Camilla Di Pardo, Teresa Molfetta, Eye Clinic Research Group, Marco Coassin, Roberto Dell’Omo, Francesco Boscia, Giovanni Alessio, Giancarlo Sborgia, Antonella Guglielmi, Giacomo Scotti, Marida Gaudiomonte, Roberto Semeraro
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionInverted Internal Limiting Membrane (ILM)-flap technique demonstrated its effectiveness, in terms of anatomical closure rate and visual acuity recovery for high myopic macular holes. We evaluated macular function after a successful invert
Externí odkaz:
https://doaj.org/article/fbdb8963a33e451990c48da6993a04c7
Akademický článek
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Autor:
Britt Östlund, Monica Malvezzi, Susanne Frennert, Michael Funk, Jose Gonzalez-Vargas, Kilian Baur, Dimitris Alimisis, Freygardur Thorsteinsson, Antonio Alonso-Cepeda, Guillaume Fau, Florian Haufe, Massimo Di Pardo, Juan C. Moreno
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
IntroductionSocial robots are accompanied by high expectations of what they can bring to society and in the healthcare sector. So far, promising assumptions have been presented about how and where social robots are most relevant. We know that the ind
Externí odkaz:
https://doaj.org/article/7191572e64b446ffbb74d670de46d60e
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Giuseppe Pepe, Salvatore Fioriniello, Federico Marracino, Luca Capocci, Vittorio Maglione, Maurizio D’Esposito, Alba Di Pardo, Floriana Della Ragione
Publikováno v:
Biomolecules, Vol 13, Iss 4, p 606 (2023)
Rett syndrome (RTT, online MIM 312750) is a devastating neurodevelopmental disorder characterized by motor and cognitive disabilities. It is mainly caused by pathogenetic variants in the X-linked MECP2 gene, encoding an epigenetic factor crucial for
Externí odkaz:
https://doaj.org/article/f8b13bb92ed44651b12c02824c1dd910