Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Servidei, Serenella"'
Autor:
Holt, James, Pritchard, Jane, Wall, Jasmine, Gamez, Josep, Oktay, YAVUZ, Macken, William L, Nesbitt, Victoria, Sansone, Valeria, Evangelista, Teresinha, Watson-Fargie, Taylor, Keddie, Stephen, Ramaratnam, Sridharan, Desai, Soaham, Yareeda, Sireesha, Rinaldi, Simon, Raga, Sharika, Menon R, Sarath, Sasidharan, Sandhya, Neshuku, Saara, Keh, Ryan, Geraldes, Ruth, Paterson, Ross W, Nortley, Ross, McFarland, Robert, Horvath, Rita, Thomas, Rhys H, Mehta, Puja R, Ambrose, Philip, Chinnery, Patrick F, Price, Olivia, Musumeci, Olimpia, Janssen, Mirian, Mancuso, Michelangelo, Dhamne, Megha, Zosmer, Maya, Ciocca, Matteo, Laura, Matilde, Skorupinska, Mariola, Househam, Liz, Clayton, Lisa, Saavedra, Lillian, Brennan, Kathryn, Wannop, Kate, Shakthi, K J S, Pizzamiglio, Chiara, Pitceathly, Robert D S, Lunn, Michael P, Brady, Stefen, De Marchi, Fabiola, Galan, Lucia, Heckmann, Jeannine M, Horga, Alejandro, Molnar, Maria J, Oliveira, Acary S B, Pinto, Wladimir B V R, Primiano, Guido, Santos, Ernestina, Schoser, Benedikt, Servidei, Serenella, Sgobbi Souza, Paulo V, Venugopalan, Vishnu, Hanna, Michael G, Dimachkie, Mazen M, Machado, Pedro M, Lim, Albert, Elsaddig, Amar, Juanatey, Ana, Romeiro, Ana, Themistocleous, Andreas, Kiss-Csenki, Annamaria, Guerrero Sola, Antonio, Patil, Anuja, Duggal, Ashish, Gabriel, Carolyn, Marshall, Charles, Record, Christopher, Allen, Claire, Bearden, David, Rathna Sabapathi, DeviPriya, R, Dileep, Vecchio, Domizia, Newman, Edward, Eshun, Edwin, Foo, Eng C, Bugiardini, Enrico, Burke, Georgina, Ramdharry, Gita, Gorman, Gràinne S, Kumar, Guru, Sivasathiaseelan, Harri, Braga Farias, Igor, Smuts, Izelle, Groothuis, Jan T
Publikováno v:
European Journal of Neurology, 30, 399-412
European Journal of Neurology, 30, 2, pp. 399-412
European Journal of Neurology, 30, 2, pp. 399-412
Contains fulltext : 291815.pdf (Publisher’s version ) (Open Access) BACKGROUND AND PURPOSE: Clinical outcome information on patients with neuromuscular diseases (NMDs) who have been infected with SARS-CoV-2 is limited. The aim of this study was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3425444b8bd1e5b2e0ab6acc97180ee2
https://doi.org/10.1111/ene.15613
https://doi.org/10.1111/ene.15613
Autor:
Barbato, Francesco, Di Paolantonio, Andrea, Distefano, M, Mastrorosa, Alessia, Sabatelli, Mario, Servidei, Serenella, Luigetti, Marco
Publikováno v:
La Clinica terapeutica. 168(3)
Miller Fisher syndrome (MFS) is considered to be an uncommon variant of Guillain-Barré Syndrome. The disease is clinically characterized by acute ataxia of limbs, areflexia and ophthalmoplegia, although the set of symptoms and signs can be quite het
Autor:
Mancuso, M, Orsucci, D, Angelini, C, Bertini, E, Catteruccia, M, Pegoraro, E, Carelli, V, Valentino, Ml, Comi, Gp, Minetti, C, Bruno, C, Moggio, M, Ienco, Ec, Mongini, T, Vercelli, L, Primiano, Guido Alessandro, Servidei, Serenella, Tonin, P, Scarpelli, M, Toscano, A, Musumeci, O, Moroni, I, Uziel, G, Santorelli, Fm, Nesti, C, Filosto, M, Lamperti, C, Zeviani, M, Siciliano, G.
Myoclonus is a possible manifestation of mitochondrial disorders, and its presence is considered, in association with epilepsy and the ragged red fibers, pivotal for the syndromic diagnosis of MERRF (myoclonic epilepsy with ragged red fibers). Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0f114a996606433a37f54d784a13fae8
http://hdl.handle.net/11577/2806259
http://hdl.handle.net/11577/2806259
Autor:
Bonilla, Eduardo, Schmidt, Beny, Samitt, Craig E., Miranda, Armand F., Hays, Arthur P., De Oliveira, Acary B.S., Chang, Hai Won, Servidei, Serenella, Ricci, Enzo, Younger, David S., Dimauro, Salvatore
Dystrophin is the gene product that is affected in Duchenne muscular dystrophy (DMD). Antibodies against dystrophin were used to study the protein in muscle fibers of carriers of the gene. The results showed that DMD carriers have normal and dystroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f509299204e6dfb1efb84afd26018cfc
https://europepmc.org/articles/PMC1880814/
https://europepmc.org/articles/PMC1880814/
Autor:
Horvath, Rita, Kemp, John P, Tuppen, Helen AL, Hudson, Gavin, Oldfors, Anders, Marie, Suely KN, Moslemi, Ali-Reza, Servidei, Serenella, Holme, Elisabeth, Shanske, Sara, Kollberg, Gittan, Jayakar, Parul, Pyle, Angela, Marks, Harold M, Holinski-Feder, Elke, Scavina, Mena, Walter, Maggie C, Coku, Jorida, Günther-Scholz, Andrea, Smith, Paul M, McFarland, Robert, Chrzanowska-Lightowlers, Zofia MA, Lightowlers, Robert N, Hirano, Michio, Lochmüller, Hanns, Taylor, Robert W, Chinnery, Patrick F, Tulinius, Mar, DiMauro, Salvatore
Childhood-onset mitochondrial encephalomyopathies are usually severe, relentlessly progressive conditions that have a fatal outcome. However, a puzzling infantile disorder, long known as 'benign cytochrome c oxidase deficiency myopathy' is an excepti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de9e84bff669f24bd953179e5a18cdb9
Autor:
Hathazi, Denisa, Griffin, Helen, Jennings, Matthew J, Giunta, Michele, Powell, Christopher, Pearce, Sarah F, Munro, Benjamin, Wei, Wei, Boczonadi, Veronika, Poulton, Joanna, Pyle, Angela, Calabrese, Claudia, Gomez-Duran, Aurora, Schara, Ulrike, Pitceathly, Robert DS, Hanna, Michael G, Joost, Kairit, Cotta, Ana, Paim, Julia Filardi, Navarro, Monica Machado, Duff, Jennifer, Mattman, Andre, Chapman, Kristine, Servidei, Serenella, Della Marina, Adela, Uusimaa, Johanna, Roos, Andreas, Mootha, Vamsi, Hirano, Michio, Tulinius, Mar, Giri, Mamta, Hoffmann, Eric P, Lochmüller, Hanns, DiMauro, Salvatore, Minczuk, Michal, Chinnery, Patrick F, Müller, Juliane S, Horvath, Rita
Reversible infantile respiratory chain deficiency (RIRCD) is a rare mitochondrial myopathy leading to severe metabolic disturbances in infants, which recover spontaneously after 6-months of age. RIRCD is associated with the homoplasmic m.14674T>C mit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::762b824bd574cd8c92923261b07dc966
Autor:
Antonio Chiaretti, Benedetto Falsini, Filomena Pierri, Riccardo Riccardi, Serenella Servidei, Dario Marangoni
Background. Spontaneous visual improvement in people with an optic glioma (OG) of the anterior or retrochiasmatic optic pathways is rare. Objective. To evaluate the effects on visual function of nerve growth factor (NGF) eye drop administration in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::523fff830865c7ae4bfbd3adf03c1275
https://hdl.handle.net/11368/3002716
https://hdl.handle.net/11368/3002716