RAINERO, Innocenzo

RAINERO, Innocenzo  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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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 comparison of familial and sporadic migraine in a headache clinic population 2002 RAINERO I; VALFRÈ W; GENTILE S; LO GIUDICE R; FERRERO M; SAVI L; PINESSI L
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 mathematical model for the evaluation of iron transport across the blood-cerebrospinal fluid barrier in neurodegenerative diseases 2020 Ficiara, E; D'Agata, F; Ansari, S; Boschi, S; Rainero, I; Priano, L; Cattaldo, S; Abollino, O; Cavalli, R; Guiot, C
A new Italian pedigree with early-onset Alzheimer's disease 1994 RAINERO I; BERGAMINI L; BRUNI AC ;FERINI-STRAMBI L; FONCIN JF; GEI G; MACCIARDI F; MONTESI MP; PINESSI L; VAULA G
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 network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia 2017 Fernando Palluzzi, Raffaele Ferrari, Francesca Graziano, Valeria Novelli, Giacomina Rossi, Daniela Galimberti, Innocenzo Rainero, Luisa Benussi, Benedetta Nacmias, Amalia C. Bruni, Daniele Cusi, Erika Salvi, Barbara Borroni, Mario Grassi
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 novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities 2010 Bachetti T; Di Zanni E; Lantieri F; Caroli F; Regis S; Filocamo M; Rainero I; Gallone S; Cilia R; Romano S; Savoiardo M; Pareyson D; Biancheri R; Ravazzolo R; Ceccherini I
A Novel PSEN1 Variant Leading to Posterior Cortical Atrophy: A Case Report 2023 Roveta, Fausto; Marcinnò, Andrea; Grassini, Alberto; Ferrandes, Fabio; Cermelli, Aurora; Boschi, Silvia; Gallone, Salvatore; Atzori, Cristiana; Imperiale, Daniele; Dentelli, Patrizia; Pasini, Barbara; Brusco, Alfredo; Rubino, Elisa; Rainero, Innocenzo
A polymorphism in the interleukin-1α gene influences the clinical features of migraine 2002 RAINERO I; PINESSI L; SALANI G; VALFRÈ W; RIVOIRO C; SAVI L; GENTILE S; GIUDICE RL; GRIMALDI LM
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
Abdominal pain associated with musical hallucinations: a case report 2007 GENTILE S; FERRERO M; GIUDICE RL; RAINERO I; PINESSI L
Abnormal 5-HT1D receptor function in chronic tension-type headache: A neuroendocrine study with sumatriptan 2001 Rainero I; Valfre' W; Savi L; Rivoiro C; Del Rizzo P; Limone P; Amanzio M; Pollo A; Benedetti F; Pinessi L
Abnormal 5-HT1D receptor function in cluster headache: A neuroendocrine study with sumatriptan 2003 PINESSI L; RAINERO I; VALFRE' W; LO GIUDICE R; FERRERO M; RIVOIRO C; ARVAT E; GIANOTTI L; DEL RIZZO P; LIMONE P
Absence of linkage between the interleukin-6 gene (-174 G/C) polymorphism and migraine 2003 RAINERO I; SALANI G; VALFRÈ W; SAVI L; RIVOIRO C; FERRERO M; PINESSI L; GRIMALDI LM