Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Graziana Tavilla"'
Autor:
Laura Ciatto, Massimo Pullia, Graziana Tavilla, Biagio Dauccio, Daniela Messina, Maria Cristina De Cola, Angelo Quartarone, Roberta Cellini, Mirjam Bonanno, Rocco Salvatore Calabrò
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2148 (2023)
Parkinson’s disease (PD) is a neurodegenerative disorder characterized by motor and non-motor alterations. Typical motor symptoms include resting tremors, bradykinesia (hypokinesia or akinesia), muscular stiffness, gait alterations, and postural in
Externí odkaz:
https://doaj.org/article/17c0db17ecf94b88a3f1f9708dc31993
Autor:
Gaetano Caramori, Michele Gaeta, Olimpia Musumeci, Antonio Toscano, Lucia Monaco, Graziana Tavilla, Paolo Ruggeri
Publikováno v:
Neurological Sciences. 41:2175-2184
Late-Onset Pompe Disease (LOPD) is characterized by progressive limb-girdle muscle weakness and respiratory dysfunction. Diaphragm is the most impaired muscle in LOPD and its dysfunction cause major respiratory symptoms. The aim of this study was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc7e5ee3f93244db1741993a99841a2
https://doi.org/10.1007/s10072-020-04316-6
https://doi.org/10.1007/s10072-020-04316-6
Autor:
Graziana Tavilla, Olimpia Musumeci, Antonio Armando Caragliano, Marcello Longo, Sergio Vinci, Antonio Toscano, Anna Ciranni, Francesca Granata, Agostino Tessitore, Antonio Pitrone, Enricomaria Mormina
Pompe disease is a rare hereditary metabolic disorder caused by α-glucosidase (GAA) deficiency. The late-onset form of the disease (LOPD) is considered a multisystemic disorder which could involve vascular system with cerebrovascular abnormalities s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f767eab1757e0663dcec20ff399ce10
http://hdl.handle.net/11570/3178056
http://hdl.handle.net/11570/3178056
Autor:
V. Montano, Massimiliano Filosto, Francesco Gruosso, Serenella Servidei, Angela Modenese, Giacomo P. Comi, Gabriele Siciliano, Silvia Marchet, Maria Lucia Valentino, Graziana Tavilla, Michelangelo Mancuso, Costanza Lamperti, Valerio Carelli, Paola Tonin, Guido Primiano, T. Mongini, Olimpia Musumeci, Megi Meneri, Antonio Toscano, Sara Bortolani
Publikováno v:
Neurology: Genetics
article-version (Version of Record) 3
article-version (Version of Record) 3
ObjectiveTo determine whether a set of functional tests, clinical scales, patient-reported questionnaires, and specific biomarkers can be considered reliable outcome measures in patients with primary mitochondrial myopathy (PMM), we analyzed a cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28852ea329033b3671a973ba2b5b1f6c
https://pubmed.ncbi.nlm.nih.gov/33209982
https://pubmed.ncbi.nlm.nih.gov/33209982
Autor:
Montano, VINCENZO GIOVANNI, Gruosso, Francesco, Valerio, Carelli, Giacomo Pietro Comi, Massimiliano, Filosto, Costanza, Lamperti, Tiziana, Mongini, Olimpia, Musumeci, Serenella, Servidei, Paola, Tonin, Antonio, Toscano, Angela, Modenese, Guido, Primiano, Maria Lucia Valentino, Sara, Bortolani, Silvia, Marchet, Megi, Meneri, Graziana, Tavilla, Siciliano, Gabriele, Mancuso, Michelangelo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3728::85eca972fe4498381e477fa93e7059c8
http://hdl.handle.net/11568/1059114
http://hdl.handle.net/11568/1059114
Autor:
Grazia Maria Igea Falcone, Filippo M. Santorelli, Antonio Toscano, Graziana Tavilla, Olimpia Musumeci, Alessandra Tessa
Publikováno v:
Journal of the Neurological Sciences. 429:118261
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c4cf37d9c50e98abbd7da6690e85bbc
https://doi.org/10.1016/j.jns.2021.118261
https://doi.org/10.1016/j.jns.2021.118261