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of 138
pro vyhledávání: '"Pani, C"'
Publikováno v:
In Composites Part A 2007 38(4):1174-1182
Publikováno v:
In Engineering Fracture Mechanics 2007 74(4):500-514
Akademický článek
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Autor:
Bandres‐Ciga, S, Noyce, AJ, Hemani, G, Nicolas, A, Calvo, A, Mora, G, Arosio, A, Barberis, M, Bartolomei, I, Battistini, S, Benigni, M, Borghero, G, Brunetti, M, Cammarosano, S, Cannas, A, Canosa, A, Capasso, M, Caponnetto, C, Caredda, C, Carrera, P, Casale, F, Cavallaro, S, Chiò, A, Colletti, T, Conforti, FL, Conte, A, Corrado, L, Costantino, E, D'Alfonso, S, Fasano, A, Femiano, C, Ferrarese, C, Fini, N, Floris, G, Fuda, G, Giannini, F, Grassano, M, Ilardi, A, La Bella, V, Lattante, S, Logroscino, G, Logullo, FO, Loi, D, Lunetta, C, Mancardi, G, Mandich, P, Mandrioli, J, Manera, U, Marangi, G, Marinou, K, Marrali, G, Marrosu, MG, Mazzini, L, Melis, M, Messina, S, Moglia, C, Monsurro, MR, Mosca, L, Occhineri, P, Origone, P, Pani, C, Penco, S, Petrucci, A, Piccirillo, G, Pirisi, A, Pisano, F, Pugliatti, M, Restagno, G, Ricci, C, Rita Murru, M, Riva, N, Sabatelli, M, Salvi, F, Santarelli, M, Sideri, R, Simone, I, Spataro, R, Tanel, R, Tedeschi, G, Tranquilli, S, Tremolizzo, L, Trojsi, F, Volanti, P, Zollino, M, Abramzon, Y, Arepalli, S, Baloh, RH, Bowser, R, Brady, CB, Brice, A, Broach, J, Campbell, RH, Camu, W, Chia, R, Cooper‐Knock, J, Cusi, D, Ding, J, Drepper, C, Drory, VE, Dunckley, TL, Eicher, JD, Faghri, F, Feldman, E, Kay Floeter, M, Fratta, P, Geiger, JT, Gerhard, G, Gibbs, JR, Gibson, SB, Glass, JD, Hardy, J, Harms, MB, Heiman‐Patterson, TD, Hernandez, DG, Jansson, L, Kamel, F, Kirby, J, Kowall, NW, Laaksovirta, H, Landi, F, Le Ber, I, Lumbroso, S, MacGowan, DJL, Maragakis, NJ, Mouzat, K, Murphy, NA, Myllykangas, L, Nalls, MA, Orrell, RW, Ostrow, LW, Pamphlett, R, Pickering‐Brown, S, Pioro, E, Pliner, HA, Pulst, SM, Ravits, JM, Renton, AE, Rivera, A, Robbrecht, W, Rogaeva, E, Rollinson, S, Rothstein, JD, Salvi, E, Scholz, SW, Sendtner, M, Shaw, PJ, Sidle, KC, Simmons, Z, Singleton, AB, Stone, DC, Sulkava, R, Tienari, PJ, Traynor, BJ, Trojanowski, JQ, Troncoso, JC, Van Damme, P, Van Deerlin, VM, Van Den Bosch, L, Zinman, L, Stone, DJ
Publikováno v:
Annals of neurology 85 (2019): 470–481. doi:10.1002/ana.25431
info:cnr-pdr/source/autori:Bandres-Ciga S; Noyce AJ; Hemani G; Nicolas A; Calvo A; Mora G; Arosio A; Barberis M; Bartolomei I; Battistini S; Benigni M; Borghero G; Brunetti M; Cammarosano S; Cannas A; Canosa A; Capasso M; Caponnetto C; Caredda C; Carrera P; Casale F; Cavallaro S; Chiò A; Colletti T; Conforti FL; Conte A; Corrado L; Costantino E; D'Alfonso S; Fasano A; Femiano C; Ferrarese C; Fini N; Floris G; Fuda G; Giannini F; Grassano M; Ilardi A; La Bella V; Lattante S; Logroscino G; Logullo FO; Loi D; Lunetta C; Mancardi G; Mandich P; Mandrioli J; Manera U; Marangi G; Marinou K; Marrali G; Marrosu MG; Mazzini L; Melis M; Messina S; Moglia C; Monsurro MR; Mosca L; Occhineri P; Origone P; Pani C; Penco S; Petrucci A; Piccirillo G; Pirisi A; Pisano F; Pugliatti M; Restagno G; Ricci C; Rita Murru M; Riva N; Sabatelli M; Salvi F; Santarelli M; Sideri R; Simone I; Spataro R; Tanel R; Tedeschi G; Tranquilli S; Tremolizzo L; Trojsi F; Volanti P; Zollino M; Abramzon Y; Arepalli S; Baloh RH; Bowser R; Brady CB; Brice A; Broach J; Campbell RH; Camu W; Chia R; Cooper-Knock J; Cusi D; Ding J; Drepper C; Drory VE; Dunckley TL; Eicher JD; Faghri F; Feldman E; Kay Floeter M; Fratta P; Geiger JT; Gerhard G; Gibbs JR; Gibson SB; Glass JD; Hardy J; Harms MB; Heiman-Patterson TD; Hernandez DG; Jansson L; Kamel F; Kirby J; Kowall NW; Laaksovirta H; Landi F; Le Ber I; Lumbroso S; MacGowan DJL; Maragakis NJ; Mouzat K; Murphy NA; Myllykangas L; Nalls MA; Orrell RW; Ostrow LW; Pamphlett R; Pickering-Brown S; Pioro E; Pliner HA; Pulst SM; Ravits JM; Renton AE; Rivera A; Robbrecht W; Rogaeva E; Rollinson S; Rothstein JD; Salvi E; Scholz SW; Sendtner M; Shaw PJ; Sidle KC; Simmons Z; Singleton AB; Stone DC; Sulkava R; Tienari PJ; Traynor BJ; Trojanowski JQ; Troncoso JC; Van Damme P; Van Deerlin VM; Van Den Bosch L; Zinman L; Stone DJ;/titolo:Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis/doi:10.1002%2Fana.25431/rivista:Annals of neurology/anno:2019/pagina_da:470/pagina_a:481/intervallo_pagine:470–481/volume:85
2019, ' Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis ', Annals of Neurology, vol. 85, no. 4, pp. 470-481 . https://doi.org/10.1002/ana.25431
Annals of Neurology
Annals of Neurology, Wiley, 2019, 85 (4), pp.470-481. ⟨10.1002/ana.25431⟩
info:cnr-pdr/source/autori:Bandres-Ciga S; Noyce AJ; Hemani G; Nicolas A; Calvo A; Mora G; Arosio A; Barberis M; Bartolomei I; Battistini S; Benigni M; Borghero G; Brunetti M; Cammarosano S; Cannas A; Canosa A; Capasso M; Caponnetto C; Caredda C; Carrera P; Casale F; Cavallaro S; Chiò A; Colletti T; Conforti FL; Conte A; Corrado L; Costantino E; D'Alfonso S; Fasano A; Femiano C; Ferrarese C; Fini N; Floris G; Fuda G; Giannini F; Grassano M; Ilardi A; La Bella V; Lattante S; Logroscino G; Logullo FO; Loi D; Lunetta C; Mancardi G; Mandich P; Mandrioli J; Manera U; Marangi G; Marinou K; Marrali G; Marrosu MG; Mazzini L; Melis M; Messina S; Moglia C; Monsurro MR; Mosca L; Occhineri P; Origone P; Pani C; Penco S; Petrucci A; Piccirillo G; Pirisi A; Pisano F; Pugliatti M; Restagno G; Ricci C; Rita Murru M; Riva N; Sabatelli M; Salvi F; Santarelli M; Sideri R; Simone I; Spataro R; Tanel R; Tedeschi G; Tranquilli S; Tremolizzo L; Trojsi F; Volanti P; Zollino M; Abramzon Y; Arepalli S; Baloh RH; Bowser R; Brady CB; Brice A; Broach J; Campbell RH; Camu W; Chia R; Cooper-Knock J; Cusi D; Ding J; Drepper C; Drory VE; Dunckley TL; Eicher JD; Faghri F; Feldman E; Kay Floeter M; Fratta P; Geiger JT; Gerhard G; Gibbs JR; Gibson SB; Glass JD; Hardy J; Harms MB; Heiman-Patterson TD; Hernandez DG; Jansson L; Kamel F; Kirby J; Kowall NW; Laaksovirta H; Landi F; Le Ber I; Lumbroso S; MacGowan DJL; Maragakis NJ; Mouzat K; Murphy NA; Myllykangas L; Nalls MA; Orrell RW; Ostrow LW; Pamphlett R; Pickering-Brown S; Pioro E; Pliner HA; Pulst SM; Ravits JM; Renton AE; Rivera A; Robbrecht W; Rogaeva E; Rollinson S; Rothstein JD; Salvi E; Scholz SW; Sendtner M; Shaw PJ; Sidle KC; Simmons Z; Singleton AB; Stone DC; Sulkava R; Tienari PJ; Traynor BJ; Trojanowski JQ; Troncoso JC; Van Damme P; Van Deerlin VM; Van Den Bosch L; Zinman L; Stone DJ;/titolo:Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis/doi:10.1002%2Fana.25431/rivista:Annals of neurology/anno:2019/pagina_da:470/pagina_a:481/intervallo_pagine:470–481/volume:85
2019, ' Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis ', Annals of Neurology, vol. 85, no. 4, pp. 470-481 . https://doi.org/10.1002/ana.25431
Annals of Neurology
Annals of Neurology, Wiley, 2019, 85 (4), pp.470-481. ⟨10.1002/ana.25431⟩
OBJECTIVE: To identify shared polygenic risk and causal associations in amyotrophic lateral sclerosis (ALS). METHODS: Linkage disequilibrium score regression and Mendelian randomization were applied in a large-scale, data-driven manner to explore gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ec44e96e87becc7f1c928039052519
http://hdl.handle.net/11591/406432
http://hdl.handle.net/11591/406432
Autor:
Manes, Marta, Benussi, Alberto, Alberici, Antonella, Di Gregorio, E, Boccone, L, Premi, Enrico, Mitro, N, Pasolini, Mp, Pani, C, Paghera, Barbara, Perani, Daniela, Orsi, L, Costanzi, C, Ferrero, M, Zoppo, A, Tempia, A, Caruso, D, Grassi, Mario, Padovani, Alessandro, Brusco, Alfredo, Borroni, Barbara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3662::08cfbcf74ac23f926a49b52e9d3b74ea
http://hdl.handle.net/11379/516499
http://hdl.handle.net/11379/516499
Autor:
Manes, M, Alberici, A, Di Gregorio, E, Boccone, L, Premi, E, Mitro, N, Pasolini, Maria Pia, Pani, C, Paghera, B, Perani, D, Orsi, Lorenzo, Costanzi, C, Ferrero, M, Zoppo, A, Tempia, F, Caruso, D, Grassi, M, Padovani, A, Brusco, Alessandro, Borroni, B.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3662::381f791669a1ab831b75342b56c514aa
http://hdl.handle.net/11379/501911
http://hdl.handle.net/11379/501911
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, 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
Publikováno v:
European Journal of Transport and Infrastructure Research, Vol 15, Iss 4 (2015)
European journal of transport and infrastructure research
Scopus-Elsevier
European journal of transport and infrastructure research
Scopus-Elsevier
Vessel arrival uncertainty in ports has become a very common problem worldwide. Although ship operators have to notify the Estimated Time of Arrival (ETA) at predetermined time intervals, they frequently have to update the latest ETA due to unforesee