Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Anna Sagnelli"'
Autor:
Antonio Ziello, Cristina Scavone, Maria Elena Di Battista, Simona Salvatore, Daniele Di Giulio Cesare, Ornella Moreggia, Lia Allegorico, Anna Sagnelli, Stefano Barbato, Valentino Manzo, Annalisa Capuano, Giorgia Teresa Maniscalco
Publikováno v:
Brain Sciences, Vol 11, Iss 7, p 890 (2021)
Background. The so-called “vaccine hesitancy” still represents a common phenomenon that undermines the effectiveness of vaccination campaigns. In 2020, the Italian Medicines Agency recommended to bring forward the flu vaccination campaign, whose
Externí odkaz:
https://doaj.org/article/685935fc0de3409b8afcf39f86225e9c
Autor:
Francesca Trojsi, Anna Sagnelli, Nicola Vanacore, Giovanni Piccirillo, Luca Daniele, Francesco Izzo, Anna Laiola, Alfonso Di Costanzo, Giovanni Savettieri, Maria Rosaria Monsurrò, Gioacchino Tedeschi
Publikováno v:
Annali dell'Istituto Superiore di Sanità, Vol 48, Iss 3, Pp 287-291 (2012)
BACKGROUND: Physical activity and occupational exposures appeared to play a relevant role in pathogenesis of amyotrophic lateral sclerosis (ALS), a neurodegenerative disease of unknown origin. MATERIALS AND METHODS: We aimed to make an overview of th
Externí odkaz:
https://doaj.org/article/00a82054b55f495b81a84363eac4b0d2
Autor:
Marta Dossena, Gloria Bedini, Paola Rusmini, Elisa Giorgetti, Alessandra Canazza, Valentina Tosetti, Ettore Salsano, Anna Sagnelli, Caterina Mariotti, Cinzia Gellera, Stefania Elena Navone, Giovanni Marfia, Giulio Alessandri, Fabio Corsi, Eugenio Agostino Parati, Davide Pareyson, Angelo Poletti
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e112746 (2014)
Spinal and bulbar muscular atrophy (SBMA) or Kennedy's disease is an X-linked CAG/polyglutamine expansion motoneuron disease, in which an elongated polyglutamine tract (polyQ) in the N-terminal androgen receptor (ARpolyQ) confers toxicity to this pro
Externí odkaz:
https://doaj.org/article/0823a55f6275454f8f227e0deaa25077
Autor:
Francesca Trojsi, Anna Sagnelli, Giovanni Cirillo, Giovanni Piccirillo, Cinzia Femiano, Francesco Izzo, Maria Rosaria Monsurrò, Gioacchino Tedeschi
Publikováno v:
Case Reports in Medicine, Vol 2012 (2012)
The concurrence of amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) is extremely rare. We reported the case of a 33-year-old woman with a past history of paresthesias at the right hand, who developed progressive quadriparesis with musc
Externí odkaz:
https://doaj.org/article/3d1510814a3a4a599fb55839ec8aff54
Autor:
Stefano Barbato, Maria Elena Di Battista, Giorgia Teresa Maniscalco, Ornella Moreggia, Antonio Rosario Ziello, Simona Salvatore, Lia Allegorico, Anna Sagnelli, Valentino Manzo, Annalisa Capuano, Daniele Di Giulio Cesare, Cristina Scavone
Publikováno v:
Brain Sciences
Volume 11
Issue 7
Brain Sciences, Vol 11, Iss 890, p 890 (2021)
Volume 11
Issue 7
Brain Sciences, Vol 11, Iss 890, p 890 (2021)
Background. The so-called “vaccine hesitancy” still represents a common phenomenon that undermines the effectiveness of vaccination campaigns. In 2020, the Italian Medicines Agency recommended to bring forward the flu vaccination campaign, whose
Autor:
Valentino Manzo, Massimo Napolitano, Simona Salvatore, Angelo Ranieri, Mariana Rippa, Gennaro Alfieri, Rosaria Renna, Giovanna Servillo, Anna Sagnelli, Ciro Florio, Katia Longo, Paolo Candelaresi, Giorgia Teresa Maniscalco, Walter Di Iorio
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 41(Suppl 2)
Autor:
Laura Fadda, Franco Taroni, Claudia Ciano, Davide Pareyson, L Melzi, Dante Facchetti, Daniela Di Bella, Giuseppe Piscosquito, Anna Sagnelli, Ettore Salsano, Antonio Morico
Publikováno v:
Journal of the Peripheral Nervous System. 22:59-63
We report the first Italian family affected by hereditary gelsolin amyloidosis (HGA), a rare autosomal dominant disease characterized by adult-onset slowly progressive cranial neuropathy, lattice corneal dystrophy, and cutis laxa. The index case was
Autor:
V. La Bella, Antonio E. Elia, Anna Sagnelli, Alfonsa Claudia Taiello, B. Reggiori, Maria Rosaria Monsurrò, G. Tedeschi, Stefania Lalli, Alberto Albanese
Publikováno v:
European Journal of Neurology. 23:45-52
Background and purpose: Tauroursodeoxycholic acid (TUDCA) is a hydrophilic bile acid that is produced in the liver and used for treatment of chronic cholestatic liver diseases. Experimental studies suggest that TUDCA may have cytoprotective and anti-
Autor:
Graziana Scigliuolo, Anna Sagnelli, Riccardo Benti, Luisa Chiapparini, Davide Pareyson, Daniela Di Bella, Davide Tonduti, Ettore Salsano, Giorgio Marotta, Laura Farina, Franco Taroni, Monica Consonni, Stefania Magri
Publikováno v:
Journal of Neurology. 263:591-593
Autor:
Alessandro Prelle, Carlo Casali, Anna Pichiecchio, Stefania Magri, Chiara Pisciotta, Yukiko K. Hayashi, Matilde Laura, Davide Pareyson, Paola Saveri, Maurizio Moggio, Michela Ripolone, Emanuele Buratti, Cristiana Stuani, Ichizo Nishino, Anna Sagnelli, Franco Taroni, Andrea Cortese, Mary M. Reilly
Publikováno v:
European journal of neurology. 25(1)
Introduction Mutations in the small heat shock protein 22 gene (HSPB8) have been associated with Charcot-Marie-Tooth type 2L, distal hereditary motor neuropathy (dHMN) type IIa and, more recently, distal myopathy/myofibrillar myopathy (MFM) with prot