RUBINO, Elisa
RUBINO, Elisa
NEUROSCIENZE "RITA LEVI MONTALCINI"
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
2018-01-01 Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, McCorkindale MD, Manzoni C, Rademakers R, Graff-Radford NR, Dickson DW, Parisi JE, Boeve BF, Petersen RC, Miller BL, Seeley WW, van Swieten JC, van Rooij J, Pijnenburg Y, van der Zee J, Van Broeckhoven C, Le Ber I, Van Deerlin V, Suh E, Rohrer JD, Mead S, Graff C, Öijerstedt L, Pickering-Brown S, Rollinson S, Rossi G, Tagliavini F, Brooks WS, Dobson-Stone C, Halliday GM, Hodges JR, Piguet O, Binetti G, Benussi L, Ghidoni R, Nacmias B, Sorbi S, Bruni AC, Galimberti D, Scarpini E, Rainero I, Rubino E, Clarimon J, Lleó A, Ruiz A, Hernández I, Pastor P, Diez-Fairen M, Borroni B, Pasquier F, Deramecourt V, Lebouvier T, Perneczky R, Diehl-Schmid J, Grafman J, Huey ED, Mayeux R, Nalls MA, Hernandez D, Singleton A, Momeni P, Zeng Z, Hardy J, Robertson J, Zinman L, Rogaeva E; International FTD-Genomics Consortium (Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Wald Ouml ML, Nilsson K, Nilsson C, Mackenzie IRA, Hsiung GR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, 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, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Grazia Spillantini M, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Elena Conidi M, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EGP, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.)
A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine
2009-01-01 Rainero I; Rubino E; Negro E; Gallone S; Fenoglio P; Binello E; Gentile S; Vaula G; Pinessi L
A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura
2008-01-01 Rainero I; Rubino E; Pinessi L; Rogaeva E; St.George-Hyslop P
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
2015-01-01 Ferrari, Raffaele; Grassi, Mario; Salvi, Erika; Borroni, Barbara; Palluzzi, Fernando; Pepe, Daniele; D'Avila, Francesca; Padovani, Alessandro; Archetti, Silvana; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Galimberti, Daniela; Scarpini, Elio; Serpente, Maria; Rossi, Giacomina; Giaccone, Giorgio; Tagliavini, Fabrizio; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Bruni, Amalia C.; Maletta, Raffaele G.; Bernardi, Livia; Postiglione, Alfredo; Milan, Graziella; Franceschi, Massimo; Puca, Annibale A.; Novelli, Valeria; Barlassina, Cristina; Glorioso, Nicola; Manunta, Paolo; Singleton, Andrew; Cusi, Daniele; Hardy, John; Momeni, Parastoo
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
2019-01-01 van der Lee, Sven J; Conway, Olivia J; Jansen, Iris; Carrasquillo, Minerva M; Kleineidam, Luca; van den Akker, Erik; Hernández, Isabel; van Eijk, Kristel R; Stringa, Najada; Chen, Jason A; Zettergren, Anna; Andlauer, Till F M; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleó, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illán-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Then Bergh, Florian; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M; Indakoetxea, Begoña; Collij, Lyduine E; Scherer, Martin; Morenas-Rodríguez, Estrella; IFGC; Raffaele Ferrari,Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, AdaikalavanRamasamy, John B.J. Kwok, Carol Dobson-Stone, William S. Brooks, PeterR. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, LaurenBartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustín Ruiz,Mercè Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga,Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, GianluigiForloni, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Elio Scarpini,Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, KarinNilsson, Christer Nilsson, Ian R.A. Mackenzie, Ging-Yuek R. Hsiung, DavidM.A. Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems,Timothy D. Griffiths, Ian G. McKeith, Alan J. Thomas, P. Pietrini, Edward D.Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C. Tierney,Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Elena Alonso, RobertPerneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Alexander Kurz,Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, PeterSt. George-Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone,James B. Rowe, Johannes C.M. Schlachetzki, James Uphill, John Collinge,Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman,John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim VanLangenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa,Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto,Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri,Jørgen E. Nielsen, Lena E. Hjermind, Matthias Riemenschneider, ManuelMayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N.Rossor, Nick C. Fox, Jason D. Warren, Maria Grazia Spillantini, Huw R.Morris, Patrizia Rizzu, Peter Heutink, Julie S. Snowden, Sara Rollinson, AnnaRichardson, Alexander Gerhard, Amalia C. Bruni, Raffaele Maletta, Fran-cesca Frangipane, Chiara Cupidi, Livia Bernardi, Maria Anfossi, Maura Gallo,Maria Elena Conidi, Nicoletta Smirne, Rosa Rademakers, Matt Baker,Dennis W. Dickson, Neill R. Graff-Radford, Ronald C. Petersen, DavidKnopman, Keith A. Josephs, Bradley F. Boeve, Joseph E. Parisi, William W.Seeley, Bruce L. Miller, Anna M. Karydas, Howard Rosen, John C. vanSwieten, Elise G.P. Dopper, Harro Seelaar, Yolande A.L. Pijnenburg, PhilipScheltens, Giancarlo Logroscino, Rosa Capozzo, Valeria Novelli, Annibale A.Puca, Massimo Franceschi, Alfredo Postiglione, Graziella Milan, PaoloSorrentino, Mark Kristiansen, Huei-Hsin Chiang, Caroline Graff, FlorencePasquier, Adeline Rollin, Vincent Deramecourt, Florence Lebert, DimitriosKapogiannis, Luigi Ferrucci, Stuart Pickering-Brown, Andrew B. Singleton,John Hardy, Parastoo Momeni; Ironside, James W; van Berckel, Bart N M; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L; Pastor, Pau; Rodríguez Rodríguez, Eloy; Boeve, Bradley F; Petersen, Ronald C; Ferman, Tanis J; van Gerpen, Jay A; Reinders, Marcel J T; Uitti, Ryan J; Tárraga, Lluís; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Mercè; Zettl, Uwe K; van Schoor, Natasja M; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; de Munain, Adolfo López; Pantelyat, Alexander; Wszolek, Zbigniew K; Ross, Owen A; Dickson, Dennis W; Graff-Radford, Neill R; Knopman, David; Rademakers, Rosa; Lemstra, Afina W; Pijnenburg, Yolande A L; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F; Hemmer, Bernhard; Huisman, Martijn A; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A; Sørensen, Thorkild I A; Heutink, Peter; Sánchez-Juan, Pascual; Posthuma, Danielle; Clarimón, Jordi; Christensen, Kaare; Ertekin-Taner, Nilüfer; Scholz, Sonja W; Ramirez, Alfredo; Ruiz, Agustín; Slagboom, Eline; van der Flier, Wiesje M; Holstege, Henne
A novel neurocognitive approach for placebo analgesia in neurocognitive disorders
2019-01-01 Palermo S.; Rainero I.; Stanziano M.; Vase L.; D'Agata F.; Rubino E.; Fonio P.; Sardanelli F.; Amanzio M.
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache
2004-01-01 RAINERO I; GALLONE S; VALFRÈ W; FERRERO M; ANGILELLA G; RIVOIRO C; RUBINO E; DE MARTINO P; SAVI L; FERRONE M; PINESSI L
A review of the recent advances in neuroimaging of frontotemporal lobar degeneration
2017-01-01 D'Agata, Federico; Orsi, Laura; Cicerale, Alessandro; Rubino, Elisa; Rainero, Innocenzo; Bergui, Mauro; Pinessi, Lorenzo
A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10
2017-01-01 Giorgio, Elisa; Rubino, Elisa; Bruselles, Alessandro; Pizzi, Simone; Rainero, Innocenzo; Duca, Sergio; Sirchia, Fabio; Pasini, Barbara; Tartaglia, Marco; Brusco, Alfredo
Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration
2009-01-01 Salvatore Gallone; Maria Teresa Giordana; Elio Scarpini; Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Daniela Galimberti; Silvia Grifoni; Eliana Venturelli; Pier Luigi Acutis; Silvia Peletto; Maria Grazia Maniaci; Patrizia Ferrero; Michela Zotta; Lorenzo Pinessi
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy.
2017-01-01 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
Analysis of the DNA methylation pattern of the promoter region of calcitonin gene-related peptide 1 gene in patients with episodic migraine: An exploratory case-control study
2022-01-01 Rubino E.; Boschi S.; Giorgio E.; Pozzi E.; Marcinno' A.; Gallo E.; Roveta F.; Grassini A.; Brusco A.; Rainero I.
Antiepileptic drugs in migraine prophylaxis
2005-01-01 Gentile S; Lo Giudice R; Rainero I; Rubino E; Magaudda A; Pinessi L
APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis
2009-01-01 Rubino E; Rainero I; Ferrero M; Vaula G; Gentile S; Valfre' W; De Martino P; Negro E; Pinessi L
Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis.
2013-01-01 Rubino E; Vacca A; Govone F; De Martino P; Pinessi L; Rainero I
Aquaporin 4 gene and migraine: an association study
2008-01-01 Rubino E; Rainero I; Gallone S; Valfrè W; Berra E; Pinessi L
Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine
2012-01-01 Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G
Association analyses of genetic variants of the HCTR1 gene in migraine
2009-01-01 Rubino E; Rainero I; Gallone S; Fenoglio P; Negro E; Savi L; Pinessi L
Association between Alzheimer's Disease and the hypocretin receptor 2 gene
2011-01-01 Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Scarpini E; Pinessi L
Association between cluster headache and alcohol dehydrogenase 4 polymorphisms
2008-01-01 Rubino E; Rainero I; Gentile S; Gallone S; Fenoglio P; Gravante E; Crasto F; Pinessi L
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers | 2018 | Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, McCorkindale MD, Manzoni C, Rademakers R, Graff-Radford NR, Dickson DW, Parisi JE, Boeve BF, Petersen RC, Miller BL, Seeley WW, van Swieten JC, van Rooij J, Pijnenburg Y, van der Zee J, Van Broeckhoven C, Le Ber I, Van Deerlin V, Suh E, Rohrer JD, Mead S, Graff C, Öijerstedt L, Pickering-Brown S, Rollinson S, Rossi G, Tagliavini F, Brooks WS, Dobson-Stone C, Halliday GM, Hodges JR, Piguet O, Binetti G, Benussi L, Ghidoni R, Nacmias B, Sorbi S, Bruni AC, Galimberti D, Scarpini E, Rainero I, Rubino E, Clarimon J, Lleó A, Ruiz A, Hernández I, Pastor P, Diez-Fairen M, Borroni B, Pasquier F, Deramecourt V, Lebouvier T, Perneczky R, Diehl-Schmid J, Grafman J, Huey ED, Mayeux R, Nalls MA, Hernandez D, Singleton A, Momeni P, Zeng Z, Hardy J, Robertson J, Zinman L, Rogaeva E; International FTD-Genomics Consortium (Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Wald Ouml ML, Nilsson K, Nilsson C, Mackenzie IRA, Hsiung GR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, 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, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Grazia Spillantini M, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Elena Conidi M, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EGP, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.) | |
| A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine | 2009 | Rainero I; Rubino E; Negro E; Gallone S; Fenoglio P; Binello E; Gentile S; Vaula G; Pinessi L | |
| A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura | 2008 | Rainero I; Rubino E; Pinessi L; Rogaeva E; St.George-Hyslop P | |
| A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia | 2015 | Ferrari, Raffaele; Grassi, Mario; Salvi, Erika; Borroni, Barbara; Palluzzi, Fernando; Pepe, Daniele; D'Avila, Francesca; Padovani, Alessandro; Archetti, Silvana; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Galimberti, Daniela; Scarpini, Elio; Serpente, Maria; Rossi, Giacomina; Giaccone, Giorgio; Tagliavini, Fabrizio; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Bruni, Amalia C.; Maletta, Raffaele G.; Bernardi, Livia; Postiglione, Alfredo; Milan, Graziella; Franceschi, Massimo; Puca, Annibale A.; Novelli, Valeria; Barlassina, Cristina; Glorioso, Nicola; Manunta, Paolo; Singleton, Andrew; Cusi, Daniele; Hardy, John; Momeni, Parastoo | |
| A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity | 2019 | van der Lee, Sven J; Conway, Olivia J; Jansen, Iris; Carrasquillo, Minerva M; Kleineidam, Luca; van den Akker, Erik; Hernández, Isabel; van Eijk, Kristel R; Stringa, Najada; Chen, Jason A; Zettergren, Anna; Andlauer, Till F M; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleó, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illán-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Then Bergh, Florian; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M; Indakoetxea, Begoña; Collij, Lyduine E; Scherer, Martin; Morenas-Rodríguez, Estrella; IFGC; Raffaele Ferrari,Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, AdaikalavanRamasamy, John B.J. Kwok, Carol Dobson-Stone, William S. Brooks, PeterR. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, LaurenBartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustín Ruiz,Mercè Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga,Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, GianluigiForloni, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Elio Scarpini,Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, KarinNilsson, Christer Nilsson, Ian R.A. Mackenzie, Ging-Yuek R. Hsiung, DavidM.A. Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems,Timothy D. Griffiths, Ian G. McKeith, Alan J. Thomas, P. Pietrini, Edward D.Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C. Tierney,Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Elena Alonso, RobertPerneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Alexander Kurz,Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, PeterSt. George-Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone,James B. Rowe, Johannes C.M. Schlachetzki, James Uphill, John Collinge,Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman,John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim VanLangenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa,Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto,Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri,Jørgen E. Nielsen, Lena E. Hjermind, Matthias Riemenschneider, ManuelMayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N.Rossor, Nick C. Fox, Jason D. Warren, Maria Grazia Spillantini, Huw R.Morris, Patrizia Rizzu, Peter Heutink, Julie S. Snowden, Sara Rollinson, AnnaRichardson, Alexander Gerhard, Amalia C. Bruni, Raffaele Maletta, Fran-cesca Frangipane, Chiara Cupidi, Livia Bernardi, Maria Anfossi, Maura Gallo,Maria Elena Conidi, Nicoletta Smirne, Rosa Rademakers, Matt Baker,Dennis W. Dickson, Neill R. Graff-Radford, Ronald C. Petersen, DavidKnopman, Keith A. Josephs, Bradley F. Boeve, Joseph E. Parisi, William W.Seeley, Bruce L. Miller, Anna M. Karydas, Howard Rosen, John C. vanSwieten, Elise G.P. Dopper, Harro Seelaar, Yolande A.L. Pijnenburg, PhilipScheltens, Giancarlo Logroscino, Rosa Capozzo, Valeria Novelli, Annibale A.Puca, Massimo Franceschi, Alfredo Postiglione, Graziella Milan, PaoloSorrentino, Mark Kristiansen, Huei-Hsin Chiang, Caroline Graff, FlorencePasquier, Adeline Rollin, Vincent Deramecourt, Florence Lebert, DimitriosKapogiannis, Luigi Ferrucci, Stuart Pickering-Brown, Andrew B. Singleton,John Hardy, Parastoo Momeni; Ironside, James W; van Berckel, Bart N M; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L; Pastor, Pau; Rodríguez Rodríguez, Eloy; Boeve, Bradley F; Petersen, Ronald C; Ferman, Tanis J; van Gerpen, Jay A; Reinders, Marcel J T; Uitti, Ryan J; Tárraga, Lluís; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Mercè; Zettl, Uwe K; van Schoor, Natasja M; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; de Munain, Adolfo López; Pantelyat, Alexander; Wszolek, Zbigniew K; Ross, Owen A; Dickson, Dennis W; Graff-Radford, Neill R; Knopman, David; Rademakers, Rosa; Lemstra, Afina W; Pijnenburg, Yolande A L; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F; Hemmer, Bernhard; Huisman, Martijn A; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A; Sørensen, Thorkild I A; Heutink, Peter; Sánchez-Juan, Pascual; Posthuma, Danielle; Clarimón, Jordi; Christensen, Kaare; Ertekin-Taner, Nilüfer; Scholz, Sonja W; Ramirez, Alfredo; Ruiz, Agustín; Slagboom, Eline; van der Flier, Wiesje M; Holstege, Henne | |
| A novel neurocognitive approach for placebo analgesia in neurocognitive disorders | 2019 | Palermo S.; Rainero I.; Stanziano M.; Vase L.; D'Agata F.; Rubino E.; Fonio P.; Sardanelli F.; Amanzio M. | |
| A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache | 2004 | RAINERO I; GALLONE S; VALFRÈ W; FERRERO M; ANGILELLA G; RIVOIRO C; RUBINO E; DE MARTINO P; SAVI L; FERRONE M; PINESSI L | |
| A review of the recent advances in neuroimaging of frontotemporal lobar degeneration | 2017 | D'Agata, Federico; Orsi, Laura; Cicerale, Alessandro; Rubino, Elisa; Rainero, Innocenzo; Bergui, Mauro; Pinessi, Lorenzo | |
| A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10 | 2017 | Giorgio, Elisa; Rubino, Elisa; Bruselles, Alessandro; Pizzi, Simone; Rainero, Innocenzo; Duca, Sergio; Sirchia, Fabio; Pasini, Barbara; Tartaglia, Marco; Brusco, Alfredo | |
| Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration | 2009 | Salvatore Gallone; Maria Teresa Giordana; Elio Scarpini; Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Daniela Galimberti; Silvia Grifoni; Eliana Venturelli; Pier Luigi Acutis; Silvia Peletto; Maria Grazia Maniaci; Patrizia Ferrero; Michela Zotta; Lorenzo Pinessi | |
| Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. | 2017 | E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero; | |
| Analysis of the DNA methylation pattern of the promoter region of calcitonin gene-related peptide 1 gene in patients with episodic migraine: An exploratory case-control study | 2022 | Rubino E.; Boschi S.; Giorgio E.; Pozzi E.; Marcinno' A.; Gallo E.; Roveta F.; Grassini A.; Brusco A.; Rainero I. | |
| Antiepileptic drugs in migraine prophylaxis | 2005 | Gentile S; Lo Giudice R; Rainero I; Rubino E; Magaudda A; Pinessi L | |
| APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis | 2009 | Rubino E; Rainero I; Ferrero M; Vaula G; Gentile S; Valfre' W; De Martino P; Negro E; Pinessi L | |
| Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis. | 2013 | Rubino E; Vacca A; Govone F; De Martino P; Pinessi L; Rainero I | |
| Aquaporin 4 gene and migraine: an association study | 2008 | Rubino E; Rainero I; Gallone S; Valfrè W; Berra E; Pinessi L | |
| Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine | 2012 | Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G | |
| Association analyses of genetic variants of the HCTR1 gene in migraine | 2009 | Rubino E; Rainero I; Gallone S; Fenoglio P; Negro E; Savi L; Pinessi L | |
| Association between Alzheimer's Disease and the hypocretin receptor 2 gene | 2011 | Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Scarpini E; Pinessi L | |
| Association between cluster headache and alcohol dehydrogenase 4 polymorphisms | 2008 | Rubino E; Rainero I; Gentile S; Gallone S; Fenoglio P; Gravante E; Crasto F; Pinessi L |