المؤلفون: P M Rossini, R Di Iorio, F Vecchio, M Anfossi, C Babiloni, Marco Bozzali, A C Bruni, S F Cappa, J Escudero, F J Fraga, P Giannakopoulos, B Guntekin, G Logroscino, C Marra, F Miraglia, F Panza, F Tecchio, A Pascual-Leone, B Dubois

مصطلحات موضوعية: Uncategorised value

العلاقة: 10779/uos.23306918.v1; https://figshare.com/articles/journal_contribution/Early_diagnosis_of_Alzheimer_s_disease_the_role_of_biomarkers_including_advanced_EEG_signal_analysis_Report_from_the_IFCN-sponsored_panel_of_experts/23306918Test

الإتاحة: https://figshare.com/articles/journal_contribution/Early_diagnosis_of_Alzheimer_s_disease_the_role_of_biomarkers_including_advanced_EEG_signal_analysis_Report_from_the_IFCN-sponsored_panel_of_experts/23306918Test

المؤلفون: L. W. Bonham, N. Z. R. Steele, C. M. Karch, I. Broce, E. G. Geier, N. L. Wen, P. Momeni, J. Hardy, Z. A. Miller, M. L. Gorno-Tempini, C. P Hess, P. Lewis, B. L. Miller, W. W. Seeley, C. Manzoni, R. S. Desikan, S. E. Baranzini, R. Ferrari, J. S. Yokoyama, D. G. Hernandez, M. A. Nalls, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-stone, P. R. Schofield, G. M. Halliday, J. R. Hodges, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. padovani, C. Cruchaga, N. J. Cairns, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M. Landqvist Waldö, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G. -Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morris, J. Attems, T. D. Griffiths, I. G. McKeith, A. J. Thomas, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaros, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega-Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulos, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q. Trojanowski, J. van der Zee, M. Cruts, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmias, S. Sorbi, S. Bagnoli, I. piaceri, J. E. Nielsen, L. E. Hjermind, M. Riemenschneider, M. Mayhaus, B. Ibach, G. Gasparoni, S. Pichler, W. Gu, M. N. Rossor, N. C. Fox, J. D. Warren, M. G. Spillantini, H. R. Morris, P. Rizzu, P. Heutink, J. S. Snowden, S. Rollinson, A. Richardson, A. Gerhard, A. C. Bruni, R. Maletta, F. Frangipane, C. Cupidi, L. Bernardi, M. Anfossi, M. Gallo, M. E. Conidi, N. Smirne, R. Rademakers, M. Baker, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, D. Knopman, K. A. Josephs, B. F. Boeve, J. E. Parisi, A. M. Karydas, H. Rosen, J. C. van Swieten, E. G. P. Dopper, H. seelaar, Y. A. L. Pijnenburg, P. Scheltens, G. Logroscino, R. Capozzo, V. Novelli, A. A. puca, M. Franceschi, A. Postiglione, G. Milan, P. Sorrentino, M. Kristiansen, H. -H. Chiang, C. Graff, F. Pasquier, A. Rollin, V. Deramecourt, T. Lebouvier, D. Kapogiannis, L. Ferrucci, S. Pickering-Brown, A. B. Singleton

المساهمون: L.W. Bonham, N.Z.R. Steele, C.M. Karch, I. Broce, E.G. Geier, N.L. Wen, P. Momeni, J. Hardy, Z.A. Miller, M.L. Gorno-Tempini, C.P He, P. Lewi, B.L. Miller, W.W. Seeley, C. Manzoni, R.S. Desikan, S.E. Baranzini, R. Ferrari, J.S.Yokoyama, D. G. Hernandez, M. A. Nall, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-stone, P. R. Schofield, G. M. Halliday, J. R. Hodge, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. padovani, C. Cruchaga, N. J. Cairn, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M. Landqvist Waldö, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G. -Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morri, J. Attem, T. D. Griffith, I. G. McKeith, A. J. Thoma, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaro, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega-Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulo, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q. Trojanowski, J. van der Zee, M. Crut, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31350420; info:eu-repo/semantics/altIdentifier/wos/WOS:000477698600012; volume:9; issue:1; firstpage:10854; lastpage:10866; numberofpages:13; journal:SCIENTIFIC REPORTS; https://hdl.handle.net/2318/1894675Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85069717816

الإتاحة: https://doi.org/10.1038/s41598-019-46415-1Test
https://hdl.handle.net/2318/1894675Test

المؤلفون: A. Mishra, R. Ferrari, P. Heutink: J. Hardy, Y. Pijnenburg, D. Posthuma, on behalf of the International FTD-Genomics Consortium: R. Ferrari, D. G. Hernandez, M. A. Nalls, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-Stone, P. R. Schofield, G. M. Halliday, J. R. Hodges, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Herna´ ndez, A. Ruiz, M. Boada, B. Borroni, A. Padovani, C. Cruchaga, N. J. Cairns, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimo´ n, A. Lleo´, R. Blesa, M. Landqvist Waldo, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G-Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morris, J. Attems, T. D. Griffiths, I. G. McKeith, A. J. Thomas, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaros, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega- Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulos, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. Tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q . Trojanowski, J. van der Zee, M. Cruts, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmias, S. Sorbi, S. Bagnoli, I. Piaceri, J. E. Nielsen, L. E. Hjermind, M. Riemenschneider, M. Mayhaus, B. Ibach, G . Gasparoni, S. Pichler, W. Gu, M. N. Rossor, N. C. Fox, J. D. Warren, M. G. Spillantini, H. R. Morris, P. Rizzu, P. Heutink, J. S. Snowden, S. Rollinson, A. Richardson, A. Gerhard, A. C. Bruni, R. Maletta, F. Frangipane, C. Cupidi, L. Bernardi, M. Anfossi, M. Gallo, M. E. Conidi, N. Smirne, R. Rademakers, M. Baker, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, D. Knopman, K. A. Josephs, B. F. Boeve, J. E. Parisi, W. W. Seeley, B. L. Miller, A. M. Karydas, H. Rosen, J. C. van Swieten, E. G. P. Dopper, H. Seelaar, Y. A. L. Pijnenburg, P. Scheltens, G. Logroscino, R. Capozzo, V. Novelli, A. A. Puca, M. Franceschi, A. Postiglione, G. Milan, P. Sorrentino, M. Kristiansen, H-H. Chiang, C. Graff, F. Pasquier, A. Rollin, V. Deramecourt, T. Lebouvier, D. Kapogiannis, L. Ferrucci, S. Pickering-Brown, A. B. Singleton, J. Hardy, P. Momeni

المساهمون: A. Mishra, R. Ferrari, P. Heutink: J. Hardy, Y. Pijnenburg, D. Posthuma, on behalf of the International FTD-Genomics Consortium: R. Ferrari, D. G. Hernandez, M. A. Nall, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-Stone, P. R. Schofield, G. M. Halliday, J. R. Hodge, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Herna´ ndez, A. Ruiz, M. Boada, B. Borroni, A. Padovani, C. Cruchaga, N. J. Cairn, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimo´ n, A. Lleo´, R. Blesa, M. Landqvist Waldo¨, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G-Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morri, J. Attem, T. D. Griffith, I. G. McKeith, A. J. Thoma, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaro, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega- Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulo, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. Tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q .Trojanowski, J. van der Zee, M. Crut, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmia, S. Sorbi, S. Bagnoli, I. Piaceri, J. E. Nielsen, L. E. Hjermind, M. Riemenschneider, M. Mayhau, B. Ibach, G .Gasparoni

مصطلحات موضوعية: FTD, gene-based association study, GWAS, MAGMA, stress-signalling pathway, Allele, Apolipoproteins E, Case-Control Studie, Frontotemporal Dementia, Genetic Association Studie, Genetic Predisposition to Disease, Guanine Nucleotide Exchange Factor, Human, Membrane Transport Protein, Protective Factor, Repressor Protein, Risk Factor, alpha 1-Antitrypsin, Neurology (clinical)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28387812; info:eu-repo/semantics/altIdentifier/wos/WOS:000400069900028; volume:140; issue:5; firstpage:1437; lastpage:1446; numberofpages:10; journal:BRAIN; http://hdl.handle.net/2318/1663656Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85019611145; http://brain.oxfordjournals.orgTest/

الإتاحة: https://doi.org/10.1093/brain/awx066Test
http://hdl.handle.net/2318/1663656Test
http://brain.oxfordjournals.orgTest/

المؤلفون: R. Ferrari, D. G. Hernandez, M. A. Nalls, J. D. Rohrer, A. Ramasamy, J. B. . J. Kwok, C. Dobson Stone, W. S. Brooks William S., P. R. Schofield, G. M. Halliday, J. R. Hodges, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. Padovani, C. Cruchaga, N. J. Cairns, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M. L. Waldö, K. Nilsson, C. Nilsson, I. R. . A. Mackenzie, G. R. Hsiung, D. M. . A. Mann, J. Grafman, C. M. Morris, J. Attems, T. D. Griffiths, I. G. McKeith, A. J. Thomas, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaros, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega Cubero, E. Alonso, R. Perneczky, J. Diehl Schmid, P. Alexopoulos, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George Hyslop, G. Rossi, F. Tagliavini, G. Giaccone, J. B. Rowe, J. C. . M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q. Trojanowski, J. Van der Zee, W. Deschamps, T. Van Langenhove, M. Cruts, C. Van Broeckhoven, S. F. Cappa, I. Le Ber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmias, S. Sorbi, S. Bagnoli, I. Piaceri, J. E. Nielsen, L. E. Hjermind, M. Riemenschneider, M. Mayhaus, B. Ibach, G. Gasparoni, S. Pichler, W. Gu, M. N. Rossor, N. C. Fox, J. D. Warren, M. G. Spillantini, H. R. Morris, P. Rizzu, P. Heutink, J. S. Snowden, S. Rollinson, A. Richardson, A. Gerhard, A. C. Bruni, R. Maletta, F. Frangipane, C. Cupidi, L. Bernardi, M. Anfossi, M. Gallo, M. E. Conidi, N. Smirne, R. Rademakers, M. Baker, D. W. Dickson, N. R. Graff Radford, R. C. Petersen, D. Knopman, K. A. Josephs, B. F. Boeve, J. E. Parisi, W. W. Seeley, B. L. Miller, A. M. Karydas, H. Rosen, J. C. van Swieten, E. G. . P. Dopper, H. Seelaar, Y. A. . L. Pijnenburg, P. Scheltens, G. Logroscino, R. Capozzo, V. Novelli, A. A. Puca, M. Franceschi, A. Postiglione, G. Milan, P. Sorrentino, M. Kristiansen, H. Chiang, C. Graff, F. Pasquier, A. Rollin, V. Deramecourt, F. Lebert, D. Kapogiannis, L. Ferrucci, S. Pickering Brown, A. B. Singleton, J. Hardy, P. Momeni

المساهمون: R. Ferrari, D.G. Hernandez, M.A. Nall, J.D. Rohrer, A. Ramasamy, J.B.J. Kwok, C. Dobson Stone, W. S. Brooks William S., P.R. Schofield, G.M. Halliday, J.R. Hodge, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. Padovani, C. Cruchaga, N.J. Cairn, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M.L. Waldö, K. Nilsson, C. Nilsson, I.R.A. Mackenzie, G.R. Hsiung, D.M.A. Mann, J. Grafman, C.M. Morri, J. Attem, T.D. Griffith, I.G. Mckeith, A.J. Thoma, P. Pietrini, E.D. Huey, E.M. Wassermann, A. Baborie, E. Jaro, M.C. Tierney, P. Pastor, C. Razquin, S. Ortega Cubero, E. Alonso, R. Perneczky, J. Diehl Schmid, P. Alexopoulo, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George Hyslop, G. Rossi, F. Tagliavini, G. Giaccone, J.B. Rowe, J.C.M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V.M. Van Deerlin, M. Grossman, J.Q. Trojanowski, J. Van der Zee, W. Deschamp, T. Van Langenhove, M. Crut, C. Van Broeckhoven, S.F. Cappa, I. Le Ber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmia, S. Sorbi, S. Bagnoli, I. Piaceri, J.E. Nielsen, L.E. Hjermind, M. Riemenschneider, M. Mayhau, B. Ibach, G. Gasparoni, S. Pichler, W. Gu, M.N. Rossor

مصطلحات موضوعية: amyotrophic-lateral-sclerosi, lobar degeneration, genetic-variation, hexanucleotide repeat, susceptibility loci, diagnostic-criteria, parkinson-disease, multiple-sclerosi, Alzheimer-disease, common variants, Settore MED/26 - Neurologia, Settore BIO/13 - Biologia Applicata

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24943344; info:eu-repo/semantics/altIdentifier/wos/WOS:000338483600015; volume:13; issue:7; firstpage:686; lastpage:699; numberofpages:14; journal:LANCET NEUROLOGY; http://hdl.handle.net/2434/248950Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84902509590

الإتاحة: https://doi.org/10.1016/S1474-4422Test(14)70065-1
http://hdl.handle.net/2434/248950Test

المؤلفون: Manuel Mayhaus, Sandro Sorbi, Peter R. Schofield, A. Rollin, A. Karydas, Alessandro Padovani, Gilles Gasparoni, Peter St George-Hyslop, Carol Dobson-Stone, Stefano F. Cappa, D. S. Knopman, John Hardy, John R. Hodges, Graziella Milan, Florence Pasquier, Christopher Morris, Edward D. Huey, Marc Cruts, Y.A.L. Pijnenburg, R. C. Petersen, Elisa Rubino, P. Scheltens, Vincent Deramecourt, Neil Graff-Radford, Elio Scarpini, Ting Wang, Panagiotis Alexopoulos, Peter Heutink, Lena E. Hjermind, AB Singleton, Jordan Grafman, Elizabeth Thompson, Adrian Danek, Pietro Pietrini, Raffaele Ferrari, Innocenzo Rainero, C. Van Broeckhoven, Rosa Capozzo, Adaikalavan Ramasamy, J. van der Zee, Eric M. Wassermann, Karin Nilsson, Ging-Yuek Robin Hsiung, J. C. van Swieten, Ping Zeng, Rosa Rademakers, Siro Bagnoli, Amalia C. Bruni, Anna Richardson, Dimitrios Kapogiannis, Ian R. A. Mackenzie, Martin N. Rossor, Bruce L. Miller, Roberta Ghidoni, Raffaele Maletta, Massimo Franceschi, Rafael Blesa, Vivianna M. Van Deerlin, Christer Nilsson, Glenda M. Halliday, Jordi Clarimón, John Q. Trojanowski, Michael Tierney, Valeria Novelli, Agustín Ruiz, Didier Hannequin, Giorgio Giaccone, Elise G.P. Dopper, Nicoletta Smirne, F Tagliavini, I. Leber, Julie S. Snowden, Sara Rollinson, Alexis Brice, Ian G. McKeith, John E. Nielsen, Paolo Sorrentino, Véronique Golfier, Maura Gallo, Lauren Bartley, B. F. Boeve, Giancarlo Logroscino, Elena Alonso, Lorenzo Pinessi, Matt Baker, Nigel J. Cairns, Matthias Riemenschneider, William S. Brooks, Alexander Gerhard, Mark Kristiansen, Eric Haan, Israel Hernandez, Ekaterina Rogaeva, Jason D. Warren, Thibaud Lebouvier, Nick C. Fox, Stuart Pickering-Brown, Giacomina Rossi, Carlos Cruchaga, G. Binetti, Maria Landqvist Waldö, William W. Seeley, Jonathan D. Rohrer, Keith A. Josephs, Diego Albani, Wei Gu, Huei-Hsin Chiang, Luigi Ferrucci, H. Zhao, Howie Rosen, Pau Pastor, Alfredo Postiglione, Evelyn Jaros, Livia Bernardi, Dena G. Hernandez, Alberto Lleó, James B. Rowe, Parastoo Momeni, Maria Serpente, Huw R. Morris, Timothy D. Griffiths, Maria Grazia Spillantini, Alan J. Thomas, Maria Elena Conidi, M. Anfossi, Sabrina Pichler, Martine Vercelletto, Murray Grossman, Johannes C. M. Schlachetzki, Gianluigi Forloni, Dennis W. Dickson, Chiara Fenoglio, Olivier Piguet, John B.J. Kwok, Benedetta Nacmias, Harro Seelaar, Robert Perneczky, A. Baborie, Patrizia Rizzu, Y. Gao, Simon Mead, Janine Diehl-Schmid, Sara Ortega-Cubero, Mike A. Nalls, Daniela Galimberti, Annibale Alessandro Puca, Cristina Razquin, Mercè Boada, Johannes Attems, Luisa Benussi, Chiara Cupidi, Irene Piaceri, Xinghao Yu, Joseph E. Parisi, Alexander Kurz, John Collinge, James Uphill, Barbara Borroni, Francesca Frangipane, Caroline Graff, Bernd Ibach, D. M. A. Mann

المساهمون: Amsterdam Neuroscience - Neurodegeneration, Human genetics, Neurology, Apollo - University of Cambridge Repository, Int FTD-Genomics Consortium IFGC

المصدر: Scientific reports, vol 10, iss 1
Scientific Reports, 10(1):12184. Nature Publishing Group
Scientific reports 10(1), 12184 (2020). doi:10.1038/s41598-020-68848-9
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, George-Hyslop, P S, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Cruts, M, Van Broeckhoven, C, Cappa, S F, Leber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebouvier, T, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P, Zhao, H, Zeng, P & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9Test
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, Rowe, J B, Nielsen, J E, Hjermind, L E & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9Test
Scientific reports

مصطلحات موضوعية: 0301 basic medicine, Oncology, lcsh:Medicine, Genome-wide association study, Neurodegenerative, 631/208, 0302 clinical medicine, Leukocytes, Odds Ratio, 2.1 Biological and endogenous factors, Aetiology, Amyotrophic lateral sclerosis, lcsh:Science, Telomerase, Telomere Shortening, education.field_of_study, Multidisciplinary, 692/617, article, Mendelian Randomization Analysis, Amyotrophic Lateral Sclerosis, Asian Continental Ancestry Group, Cholesterol, European Continental Ancestry Group, Genome-Wide Association Study, Humans, Lipoproteins, LDL, Polymorphism, Single Nucleotide, Proportional Hazards Models, Telomere, Frontotemporal Dementia, Single Nucleotide, Neurology, Engineering sciences. Technology, 692/499, medicine.medical_specialty, Lipoproteins, 692/308, Population, White People, LDL, Mendelian randomization (MR) , leukocyte telomere length (LTL) , amyotrophic lateral sclerosis (ALS), 03 medical and health sciences, Medical research, Rare Diseases, Asian People, Internal medicine, Mendelian randomization, Genetics, medicine, Polymorphism, education, Genetic association, business.industry, Proportional hazards model, International FTD-Genomics Consortium, lcsh:R, Neurosciences, Odds ratio, medicine.disease, Computational biology and bioinformatics, Brain Disorders, 030104 developmental biology, Risk factors, lcsh:Q, 631/114, ALS, business, ddc:600, 030217 neurology & neurosurgery

وصف الملف: application/pdf; application/zip; text/xml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::311860380fb1414204d0afc5fcb0b1d3Test
https://doi.org/10.1038/s41598-020-68848-9Test

المؤلفون: B. Borroni, M. Grassi, M. Bianchi, A. C. Bruni, R. G. Maletta, M. Anfossi, D. Pepe, A. Cagnin, P. Caffarra, S. Cappa, F. Clerici, A. Daniele, G. B. Frisoni, L. Parnetti, R. Perri, I. Rainero, L. Tremolizzo, M. Turla, O. Zanetti, A. Padovani, D. Galimberti

المساهمون: B. Borroni, M. Grassi, M. Bianchi, A.C. Bruni, R.G. Maletta, M. Anfossi, D. Pepe, A. Cagnin, P. Caffarra, S. Cappa, F. Clerici, A. Daniele, G.B. Frisoni, D. Galimberti, L. Parnetti, R. Perri, I. Rainero, L. Tremolizzo, M. Turla, O. Zanetti, A. Padovani

مصطلحات موضوعية: Frontotemporal dementia, frontotemporal lobar degeneration, genetic, heritability, inheritance, Age of Onset, Aged, Female, Human, Italy, Male, Middle Aged, Parent, Registrie, Sex Factor, Inheritance Pattern, Medicine (all), Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23719513; info:eu-repo/semantics/altIdentifier/wos/WOS:000337918000004; volume:41; issue:2; firstpage:371; lastpage:376; numberofpages:6; journal:JOURNAL OF ALZHEIMER'S DISEASE; http://hdl.handle.net/2434/514438Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84927566601

الإتاحة: https://doi.org/10.3233/JAD-130128Test
http://hdl.handle.net/2434/514438Test

المؤلفون: D. Galimberti, C. Fenoglio, M. Serpente, C. Villa, R. Bonsi, A. Arighi, G.G. Fumagalli, R. Del Bo, B. Dell'Osso, G.P. Comi, A.C. Altamura, C. Mariani, E. Scarpini, A. C. Bruni, M. Anfossi, A. Clodomiro, C. Cupidi, B. Nacmias, S. Sorbi, I. Piaceri, S. Bagnoli, V. Bessi, A. Marcone, C. Cerami, S. F. Cappa, M. Filippi, F. Agosta, G. Magnani, G. Comi, M. Franceschi, I. Rainero, M. T. Giordana, E. Rubino, P. Ferrero, E. Rogaeva, Z. Xi, A. Confaloni, P. Piscopo, G. Bruno, G. Talarico, A. Cagnin, F. Clerici

المساهمون: D. Galimberti, C. Fenoglio, M. Serpente, C. Villa, R. Bonsi, A. Arighi, G.G. Fumagalli, R. Del Bo, A.C. Bruni, M. Anfossi, A. Clodomiro, C. Cupidi, B. Nacmia, S. Sorbi, I. Piaceri, S. Bagnoli, V. Bessi, A. Marcone, C. Cerami, S.F. Cappa, M. Filippi, F. Agosta, G. Magnani, G. Comi, M. Franceschi, I. Rainero, M.T. Giordana, E. Rubino, P. Ferrero, E. Rogaeva, Z. Xi, A. Confaloni, P. Piscopo, G. Bruno, G. Talarico, A. Cagnin, F. Clerici, B. Dell'Osso, G.P. Comi, A.C. Altamura, C. Mariani, E. Scarpini

مصطلحات موضوعية: C9ORF72, clinical presentation, dementia, frontotemporal lobar degeneration, hexanucleotide repeat expansion, late onset psychosi, phenotype, Settore MED/26 - Neurologia, Settore MED/25 - Psichiatria

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000324050500012; volume:74; issue:5; firstpage:384; lastpage:391; numberofpages:8; journal:BIOLOGICAL PSYCHIATRY; http://hdl.handle.net/2434/227800Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84882289214

الإتاحة: https://doi.org/10.1016/j.biopsych.2013.01.031Test
http://hdl.handle.net/2434/227800Test

المؤلفون: Elena Fea, Ida Colantonio, Ornella Garrone, G. Cento, G.G. Di Costanzo, Elvio G. Russi, Gianmauro Numico, Gianfilippo Bertelli, Milena Gasco, Cristina Granetto, Marco Merlano, M. Anfossi, Nicola Silvestris, Marcella Occelli

المصدر: Annals of Oncology. 20:941-945

مصطلحات موضوعية: Adult, Male, Health Knowledge, Attitudes, Practice, medicine.medical_specialty, Palliative care, Adolescent, Referral, Attitude of Health Personnel, Medical Oncology, Truth Disclosure, Young Adult, Level of consciousness, Patient Education as Topic, Neoplasms, Surveys and Questionnaires, medicine, Humans, In patient, Referral and Consultation, Aged, Aged, 80 and over, Physician-Patient Relations, business.industry, Age Factors, Cancer, Hematology, Awareness, Middle Aged, Prognosis, medicine.disease, Surgery, Patient Rights, Oncology, Health Care Surveys, Family medicine, Workforce, Female, Empathy, Communication skills, Comprehension, Training program, business, Program Evaluation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::274cbba9e331f0df27fe457b84ce139aTest
https://doi.org/10.1093/annonc/mdn709Test

المؤلفون: Sandro Sorbi, Orso Bugiani, Lorenzo Pinessi, Innocenzo Rainero, Carmine Tomaino, Livia Bernardi, B. Terni, Alfredo Postiglione, Alessandra Clodomiro, Sabina Pappatà, J. F. Foncin, R. Di Lorenzo, N. Abbamondi, Raffaele Maletta, M. Anfossi, L. Nee, Francesca Frangipane, P H St George Hyslop, A. Leotta, M. G. Muraca, Sabrina A.M. Curcio, Graziella Milan, Giorgio Giaccone, Gianfranco Puccio, Elisa Rubino, Amalia C. Bruni, Ekaterina Rogaeva, Silvana Geracitano, Rosanna Colao, Maura Gallo, Maria Grazia Spillantini, Gianluigi Forloni, Maria Mirabelli, Nicoletta Smirne, S Lio

المصدر: Neurology 74 (2010): 798–806. doi:10.1212/WNL.0b013e3181d52785
info:cnr-pdr/source/autori:Bruni AC;Bernardi L;Colao R;Rubino E;Smirne N;Frangipane F;Terni B;Curcio SA;Mirabelli M;Clodomiro A;Di Lorenzo R;Maletta R;Anfossi M;Gallo M;Geracitano S;Tomaino C;Muraca MG;Leotta A;Lio SG;Pinessi L;Rainero I;Sorbi S;Nee L;Milan G;Pappatà S;Postiglione A;Abbamondi N;Forloni G;St George Hyslop P;Rogaeva E;Bugiani O;Giaccone G;Foncin JF;Spillantini MG;Puccio G./titolo:Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation./doi:10.1212%2FWNL.0b013e3181d52785/rivista:Neurology/anno:2010/pagina_da:798/pagina_a:806/intervallo_pagine:798–806/volume:74

مصطلحات موضوعية: Adult, Male, Alzheimer disease, presenilin 1, Genotype, International Cooperation, Population, Biology, Global Health, PSEN1 mutation, History, 21st Century, Presenilin, History, 17th Century, Methionine, Gene Frequency, Alzheimer Disease, Fluorodeoxyglucose F18, Leucine, Presenilin-1, PSEN1, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, education, Prefrontal cortex, Family Health, Genetics, Memory Disorders, education.field_of_study, Brain, Articles, Middle Aged, Alzheimer's disease, medicine.disease, founder effect, Phenotype, Dorsolateral prefrontal cortex, medicine.anatomical_structure, Italy, Positron-Emission Tomography, Mutation, Mutation (genetic algorithm), Female, Neurology (clinical), Cognition Disorders

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f79a5059afdc1cd6987baed55d02717Test
http://hdl.handle.net/2318/152288Test

المؤلفون: John Hardy, Francesca Frangipane, Ekaterina Rogaeva, Silvana Geracitano, Gianfranco Puccio, Carmine Tomaino, Yosuke Wakutani, S. Pradella, Livia Bernardi, M. Anfossi, Amalia C. Bruni, Christine Sato, P. St. George-Hyslop, Parastoo Momeni, Rosanna Colao, Raffaele Maletta, T. Kawarai, Maria Mirabelli, Nicoletta Smirne, Andrew Kertesz, Joshua W. Elder, A. Costanzo, Sabrina A.M. Curcio, Maura Gallo

المصدر: Neurology. 69(2)

مصطلحات موضوعية: Proband, Adult, Genetic Markers, Male, Heterozygote, Genotype, DNA Mutational Analysis, Biology, Cohort Studies, Progranulins, Gene Frequency, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Allele, Age of Onset, Allele frequency, Aged, Phenocopy, Genetics, Aged, 80 and over, Genetic heterogeneity, Genetic Carrier Screening, Haplotype, Middle Aged, medicine.disease, Pedigree, Italy, Mutation (genetic algorithm), Mutation, Intercellular Signaling Peptides and Proteins, Dementia, Female, Neurology (clinical), Frontotemporal dementia, Chromosomes, Human, Pair 17

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f03ecc110fc922bde08a3aeab258c89eTest
https://pubmed.ncbi.nlm.nih.gov/17620543Test