Zobrazeno 1 - 10
of 524
pro vyhledávání: '"Marrosu, F"'
Autor:
Solla, P., Cannas, A., Floris, G.L., Orofino, G., Costantino, E., Boi, A., Serra, C., Marrosu, M.G., Marrosu, F.
Publikováno v:
In Progress in Neuropsychopharmacology & Biological Psychiatry 2011 35(4):1009-1013
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Marrosu, F., Santoni, F., Puligheddu, M., Barberini, L., Maleci, A., Ennas, F., Mascia, M., Zanetti, G., Tuveri, A., Biggio, G.
Publikováno v:
In Clinical Neurophysiology 2005 116(9):2026-2036
Autor:
Puligheddu, Monica, Congiu, Patrizia, Laccu, Ilaria, Figorilli, Michela, Gioi, Gioia, Polizzi, Lorenzo, Pisanu, Patrizia, Marrosu, F., Provini, Federica
Publikováno v:
In Sleep Medicine August 2017 36:75-77
Autor:
Chio, A., Battistini, Stefania, Calvo, A., Caponnetto, C., Conforti, F. L., Corbo, M., Giannini, Fabio, Mandrioli, J., Mora, G., Sabatelli, M., Ajmone, C., Mastro, E., Pain, D., Mandich, P., Penco, S., Restagno, G., Zollino, M., Surbone, A., Monsurro, M. R., Tedeschi, G., Conte, A., Luigetti, M., Lattante, S., Marangi, G., Volanti, P., Marinou, K., Papetti, L., Lunetta, C., Pintor, G. L., Salvi, F., Bartolomei, I., Quattrone, A., Gambardella, A., Logroscino, G., Simone, I., Pisano, F., Spataro, R., La Bella, V., Colletti, T., Mancardi, G., Origone, P., Sola, P., Borghero, G., Marrosu, F., Marrosu, M. G., Murru, M. R., Floris, G., Cannas, A., Piras, V., Costantino, E., Pani, C., Sotgiu, M. A., Pugliatti, M., Parish, L. D., Cossu, P., Ticca, A., Rodolico, C., Portaro, S., Ricci, Claudia, Moglia, C., Ossola, I., Brunetti, M., Barberis, M., Canosa, A., Cammarosano, S., Bertuzzo, D., Fuda, G., Ilardi, A., Manera, U., Pastore, I., Sproviero, W., Logullo, F., Tanel, R.
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Vol 85
Europe PubMed Central
Europe PubMed Central
The clinical approach to patients with amyotrophic lateral sclerosis (ALS) has been largely modified by the identification of novel genes, the detection of gene mutations in apparently sporadic patients, and the discovery of the strict genetic and cl
Autor:
Chiò, A, Mora, G, Sabatelli, M, Caponnetto, C, Lunetta, C, Traynor, B. J, Johnson, J. O, Nalls, M. A, Calvo, A, Moglia, C, Borghero, G, Trojsi, F, La Bella, V, Volanti, P, Simone, I, Salvi, F, Logullo, F. O, Riva, N, Carrera, P, Giannini, F, Mandrioli, J, Tanel, R, Capasso, M, Tremolizzo, L, Battistini, S, Murru, M. R, Origone, P, Zollino, M, Penco, S, Mazzini, L, D'Alfonso, S, Restagno, G, Brunetti, M, Barberis, M, Conforti, F. L, Logroscino, G, Bartolomei, I, Mancardi, G, Mandich, P, Marinou, K, Sideri, R, Mosca, L, Lauria Pinter, G, Corbo, M, Fini, N, Fasano, A, Arosio, A, Ferrarese, C, Tedeschi, G, Monsurrò, M. R, Piccirillo, G, Femiano, C, Bersano, A, Corrado, L, Bagarotti, A, Spataro, R, Colletti, T, Conte, A, Luigetti, M, Lattante, S, Marangi, G, Santarelli, M, Petrucci, A, Ricci, C, Benigni, M, Casale, F, Marrali, G, Fuda, G, Ossola, I, Cammarosano, S, Ilardi, A, Manera, U, Bertuzzo, D, Pisano, F, Costantino, E, Pani, C, Puddu, R, Caredda, C, Piras, V, Tranquilli, S, Cuccu, S, Corongiu, D, Melis, M, Milia, A, Marrosu, F, Marrosu, M. G, Floris, G, Cannas, A, Ticca, A, Pugliatti, M, Pirisi, A, Parish, L. D, Occhineri, P, Ortu, E, Cau, T. B, Loi, D
Publikováno v:
Neurobiology of aging 39 (2016). doi:10.1016/j.neurobiolaging.2015.11.027
info:cnr-pdr/source/autori:Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Lunetta C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Trojsi F.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Riva N.; Carrera P.; Giannini F.; Mandrioli J.; Tanel R.; Capasso M.; Tremolizzo L.; Battistini S.; Murru M.R.; Origone P.; Zollino M.; Penco S.; Mazzini L.; D'Alfonso S.; Restagno G.; Brunetti M.; Barberis M.; Conforti F.L./titolo:ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion/doi:10.1016%2Fj.neurobiolaging.2015.11.027/rivista:Neurobiology of aging/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:39
info:cnr-pdr/source/autori:Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Lunetta C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Trojsi F.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Riva N.; Carrera P.; Giannini F.; Mandrioli J.; Tanel R.; Capasso M.; Tremolizzo L.; Battistini S.; Murru M.R.; Origone P.; Zollino M.; Penco S.; Mazzini L.; D'Alfonso S.; Restagno G.; Brunetti M.; Barberis M.; Conforti F.L./titolo:ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion/doi:10.1016%2Fj.neurobiolaging.2015.11.027/rivista:Neurobiology of aging/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:39
There are indications that both familial amyotrophic lateral sclerosis (ALS) and sporadic ALS phenotype and prognosis are partly regulated by genetic and environmental factors, supporting the theory that ALS is a multifactorial disease. The aim of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ef4c52e3b93196003d7c5a00a1c58ca
http://hdl.handle.net/10807/71872
http://hdl.handle.net/10807/71872
Autor:
Chiò, A1, Borghero, G, Restagno, G, Mora, G, Drepper, C, Traynor, Bj, Sendtner, M, Brunetti, M, Ossola, I, Calvo, A, Pugliatti, M, Sotgiu, Ma, Murru, Mr, Marrosu, Mg, Marrosu, F, Marinou, K, Mandrioli, J, Sola, P, Caponnetto, C, Mancardi, G, Mandich, P, La Bella, V, Spataro, R, Conte, A, Monsurrò, Mr, Tedeschi, G, Pisano, F, Bartolomei, I, Salvi, F, Lauria Pinter, G, Simone, I, Logroscino, G, Gambardella, A, Quattrone, A, Lunetta, C, Volanti, P, Zollino, M, Penco, S, Battistini, S, Renton, Ae, Majounie, E, Abramzon, Y, Conforti, Fl, Giannini, F, Corbo, M, Sabatelli, M, Moglia, C, Cammarosano, S, Fuda, G, Canosa, A, Gallo, S, Papetti, L, Luigetti, M, Lattante, S, Marangi, G, Colletti, T, Ricci, C, Origone, P, Floris, G, Cannas, A, Piras, V, Parish, Ld, Solinas, G, Ulgheri, L, Ticca, A, Izzo, F, Laiola, A, Trojsi, F.
Publikováno v:
Brain; Vol 135
A large hexanucleotide (GGGGCC) repeat expansion in the first intron of C9ORF72, a gene located on chromosome 9p21, has been recently reported to be responsible for 40% of familial amyotrophic lateral sclerosis cases of European ancestry. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7b1331de09fc72396eac00281aea79
http://hdl.handle.net/10807/4510
http://hdl.handle.net/10807/4510
Autor:
Majounie, E1, Renton, Ae, Mok, K, Dopper, Eg, Waite, A, Rollinson, S, Chiò, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten JC, Abramzon, Y, Johnson, Jo, Sendtner, M, Pamphlett, R, Orrell, Rw, Mead, S, Sidle, Kc, Houlden, H, Rohrer, Jd, Morrison, Ke, Pall, H, Talbot, K, Ansorge, O, Hernandez, Dg, Arepalli, S, Sabatelli, M, Mora, G, Corbo, M, Giannini, F, Calvo, A, Englund, E, Borghero, G, Floris, Gl, Remes, Am, Laaksovirta, H, Mccluskey, L, Trojanowski, Jq, Van Deerlin VM, Schellenberg, Gd, Nalls, Ma, Drory, Ve, Lu, Cs, Yeh, Th, Ishiura, H, Takahashi, Y, Tsuji, S, Le Ber, I, Brice, A, Drepper, C, Williams, N, Kirby, J, Shaw, P, Hardy, J, Tienari, Pj, Heutink, P, Morris, Hr, Pickering-Brown, S, Traynor, Bj, Adamson, G, Bayer, Aj, Beck, J, Callister, Jb, Blake, Dj, Blumen, Sc, Collinge, J, Dunckley, T, Ealing, J, East, S, Elman, L, Gerhard, A, Guerreiro, Rj, Gwinn, K, Halliwell, N, Hamdalla, Hh, Hewitt, C, Ince, P, Jablonka, S, James, C, Kent, L, Knock, Jc, Lynch, T, Mahoney, C, Mann, D, Neal, J, Norris, D, O'Dowd, S, Richardson, A, Rossor, M, Rothstein, J, Scholz, Sw, Snowden, J, Stephan, Da, Toulson, G, Turner, Mr, Warren, Jd, Young, K, Weng, Yh, Kuo, Hc, Lai, Sc, Huang, Cl, Camuzat, A, Entraingues, L, Guillot-Noël, Verpillat, P, Blanc, F, Camu, W, Clerget-Darpoux, F, Corcia, P, Couratier, P, Didic, M, Dubois, B, Duyckaerts, C, Guedj, E, Golfier, V, Habert, Mo, Hannequin, D, Lacomblez, L, Meininger, V, Salachas, F, Levy, R, Michel, Bf, Pasquier, F, Puel, M, Thomas-Anterion, C, Sellal, F, Vercelletto, M, Moglia, C, Cammarosano, S, Canosa, A, Gallo, S, Brunetti, M, Ossola, I, Marinou, K, Papetti, L, Pisano, F, Pinter, Gl, Conte, A, Luigetti, M, Zollino, M, Lattante, S, Marangi, G, la Bella, V, Spataro, R, Colletti, T, Battistini, S, Ricci, C, Caponnetto, C, Mancardi, G, Mandich, P, Salvi, F, Bartolomei, I, Mandrioli, J, Sola, P, Lunetta, C, Penco, S, Monsurrò, Mr, Tedeschi, G, Conforti, Fl, Gambardella, A, Quattrone, A, Volanti, P, Floris, G, Cannas, A, Piras, V, Marrosu, F, Marrosu, Mg, Murru, Mr, Pugliatti, M, Parish, Ld, Sotgiu, A, Solinas, G, Ulgheri, L, Ticca, A, Simone, I, Logroscino, G.
Publikováno v:
The Lancet Neurology; Vol 11
Majounie, E, Renton, A E, Mok, K, Dopper, E G P, Waite, A, Rollinson, S, Chio, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J C, Abramzon, Y, Johnson, J O, Sendtner, M, Pamphlett, R, Orrell, R W, Mead, S, Sidle, K C, Houlden, H, Rohrer, J D, Morrison, K E, Pall, H, Talbot, K, Ansorge, O, Hernandez, D G, Arepalli, S, Sabatelli, M, Mora, G, Corbo, M, Giannini, F, Calvo, A, Englund, E, Borghero, G, Foris, G L, Remes, A M, Laaksovirta, H, McCluskey, L, Trojanowski, J Q, Van Deerlin, V M, Schellenberg, G D, Nalls, M A, Drory, V E, Lu, C S, Yeh, T H, Ishiura, H, Takahashi, Y, Tsuji, S, Le Ber, I, Brice, A, Drepper, C, Williams, N, Kirby, J, Shaw, P, Hardy, J, Tienari, P J, Heutink, P, Morris, H R, Pickering-Brown, S & Traynor, B J 2012, ' Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study ', Lancet Neurology, vol. 11, no. 4, pp. 323-330 . https://doi.org/10.1016/S1474-4422(12)70043-1
Lancet Neurology, 11(4), 323-330. Lancet Publishing Group
Nature Communications
Nature Communications, Nature Publishing Group, 2012, 11 (4), pp.323-30. ⟨10.1016/S1474-4422(12)70043-1⟩
Nature Communications, 2012, 11 (4), pp.323-30. ⟨10.1016/S1474-4422(12)70043-1⟩
Lancet Neurology; 11(4), pp 323-330 (2012)
Majounie, E, Renton, A E, Mok, K, Dopper, E G P, Waite, A, Rollinson, S, Chio, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J C, Abramzon, Y, Johnson, J O, Sendtner, M, Pamphlett, R, Orrell, R W, Mead, S, Sidle, K C, Houlden, H, Rohrer, J D, Morrison, K E, Pall, H, Talbot, K, Ansorge, O, Hernandez, D G, Arepalli, S, Sabatelli, M, Mora, G, Corbo, M, Giannini, F, Calvo, A, Englund, E, Borghero, G, Foris, G L, Remes, A M, Laaksovirta, H, McCluskey, L, Trojanowski, J Q, Van Deerlin, V M, Schellenberg, G D, Nalls, M A, Drory, V E, Lu, C S, Yeh, T H, Ishiura, H, Takahashi, Y, Tsuji, S, Le Ber, I, Brice, A, Drepper, C, Williams, N, Kirby, J, Shaw, P, Hardy, J, Tienari, P J, Heutink, P, Morris, H R, Pickering-Brown, S & Traynor, B J 2012, ' Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study ', Lancet Neurology, vol. 11, no. 4, pp. 323-330 . https://doi.org/10.1016/S1474-4422(12)70043-1
Lancet Neurology, 11(4), 323-330. Lancet Publishing Group
Nature Communications
Nature Communications, Nature Publishing Group, 2012, 11 (4), pp.323-30. ⟨10.1016/S1474-4422(12)70043-1⟩
Nature Communications, 2012, 11 (4), pp.323-30. ⟨10.1016/S1474-4422(12)70043-1⟩
Lancet Neurology; 11(4), pp 323-330 (2012)
International audience; BACKGROUND: We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large proportion of cases of amyotrophic lateral sclerosis (ALS) and frontotemporal deme
Autor:
Chiò, A, Mora, G, Sabatelli, M, Caponnetto, C, Traynor, B. J, Johnson, J. O, Nalls, M. A, Calvo, A, Moglia, C, Borghero, G, Monsurrò, M. R, La Bella, V, Volanti, P, Simone, I, Salvi, F, Logullo, F. O, Nilo, R, Battistini, S, Mandrioli, J, Tanel, R, Murru, M. R, Mandich, P, Zollino, M, Conforti, F. L, Brunetti, M, Barberis, M, Restagno, G, Penco, S, Lunetta, C, Giannini, F, Ricci, C, Mancardi, G, Bartolomei, I, Corbo, M, Conte, A, Luigetti, M, Lattante, S, Marangi, G, Ossola, I, Logroscino, G, Tedeschi, G, Pugliatti, M, Pinter, G. L, Glynn, S, Gibbs, J. R, Cammarosano, S, Canosa, A, Manera, U, Bertuzzo, D, Ilardi, A, Marinou, K, Sideri, R, Pisano, F, Spataro, R, Colletti, T, Floris, G, Cannas, A, Piras, V, Marrosu, F, Marrosu, M. G, Parish, L. D, Ticca, A, Pirisi, A, Ortu, E, Cau, T. B, Loi, D, Traccis, S, Fini, N, Georgoulopoulou, E, Casale, F, Marrali, G, Fuda, G, Solamone, P, Maestri, E, Mazzei, R, Cristillo, V, Puddu, R, Costantino, E, Pani, C, Caredda, C, Origone, P, Mosca, L, Capasso, M, Turri, M, Petrucci, A, Tremolizzo, L, Santarelli, M.
Publikováno v:
Neurobiology of aging (Online) 36 (2015): 1767.e3–1767.e6. doi:10.1016/j.neurobiolaging.2015.01.017
info:cnr-pdr/source/autori:Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Monsurro M.R.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Nilo R.; Battistini S.; Mandrioli J.; Tanel R.; Murru M.R.; Mandich P.; Zollino M.; Conforti F.L.; Brunetti M.; Barberis M.; Restagno G.; Penco S.; Lunetta C.; Giannini F.; Ricci C.; Mancardi G.; Bartolomei I.; Corbo M.; Conte A.; Luigetti M.; Lattante S.; Marangi G.; Ossola I.; Logroscino G.; Tedeschi G.; Pugliatti M.; Pinter G.L.; Glynn S.; Gibbs J.R.; Cammarosano S.; Canosa A.; Manera U.; Bertuzzo D.; Ilardi A.; Marinou K.; Sideri R.; Pisano F.; Spataro R.; Colletti T.; Floris G.; Cannas A.; Piras V.; Marrosu F.; Marrosu M.G.; Parish L.D.; Ticca A.; Pirisi A.; Ortu E.; Cau T.B.; Loi D.; Traccis S.; Fini N.; Georgoulopoulou E.; Casale F.; Marrali G.; Fuda G.; Solamone P.; Maestri E.; Mazzei R.; Cristillo V.; Puddu R.; Costantino E.; Pani C.; Caredda C.; Origone P.; Mosca L.; Capasso M.; Turri M.; Petrucci A.; Tremolizzo L.; Santarelli M./titolo:CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients/doi:10.1016%2Fj.neurobiolaging.2015.01.017/rivista:Neurobiology of aging (Online)/anno:2015/pagina_da:1767.e3/pagina_a:1767.e6/intervallo_pagine:1767.e3–1767.e6/volume:36
info:cnr-pdr/source/autori:Chio A.; Mora G.; Sabatelli M.; Caponnetto C.; Traynor B.J.; Johnson J.O.; Nalls M.A.; Calvo A.; Moglia C.; Borghero G.; Monsurro M.R.; La Bella V.; Volanti P.; Simone I.; Salvi F.; Logullo F.O.; Nilo R.; Battistini S.; Mandrioli J.; Tanel R.; Murru M.R.; Mandich P.; Zollino M.; Conforti F.L.; Brunetti M.; Barberis M.; Restagno G.; Penco S.; Lunetta C.; Giannini F.; Ricci C.; Mancardi G.; Bartolomei I.; Corbo M.; Conte A.; Luigetti M.; Lattante S.; Marangi G.; Ossola I.; Logroscino G.; Tedeschi G.; Pugliatti M.; Pinter G.L.; Glynn S.; Gibbs J.R.; Cammarosano S.; Canosa A.; Manera U.; Bertuzzo D.; Ilardi A.; Marinou K.; Sideri R.; Pisano F.; Spataro R.; Colletti T.; Floris G.; Cannas A.; Piras V.; Marrosu F.; Marrosu M.G.; Parish L.D.; Ticca A.; Pirisi A.; Ortu E.; Cau T.B.; Loi D.; Traccis S.; Fini N.; Georgoulopoulou E.; Casale F.; Marrali G.; Fuda G.; Solamone P.; Maestri E.; Mazzei R.; Cristillo V.; Puddu R.; Costantino E.; Pani C.; Caredda C.; Origone P.; Mosca L.; Capasso M.; Turri M.; Petrucci A.; Tremolizzo L.; Santarelli M./titolo:CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients/doi:10.1016%2Fj.neurobiolaging.2015.01.017/rivista:Neurobiology of aging (Online)/anno:2015/pagina_da:1767.e3/pagina_a:1767.e6/intervallo_pagine:1767.e3–1767.e6/volume:36
Mutations in CHCHD10 have recently been described as a cause of frontotemporal dementia (FTD) comorbid with amyotrophic lateral sclerosis (ALS). The aim of this study was to assess the frequency and clinical characteristics of CHCHD10 mutations in It