RAINERO, Innocenzo
RAINERO, Innocenzo
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 comparison of familial and sporadic migraine in a headache clinic population
2002-01-01 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
2009-01-01 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 mathematical model for the evaluation of iron transport across the blood-cerebrospinal fluid barrier in neurodegenerative diseases
2020-01-01 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
1994-01-01 RAINERO I; BERGAMINI L; BRUNI AC ;FERINI-STRAMBI L; FONCIN JF; GEI G; MACCIARDI F; MONTESI MP; PINESSI L; VAULA G
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia
2017-01-01 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
2019-01-01 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
2010-01-01 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 polymorphism in the interleukin-1α gene influences the clinical features of migraine
2002-01-01 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
2004-01-01 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
Abdominal pain associated with musical hallucinations: a case report
2007-01-01 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
2001-01-01 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
2003-01-01 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
2003-01-01 RAINERO I; SALANI G; VALFRÈ W; SAVI L; RIVOIRO C; FERRERO M; PINESSI L; GRIMALDI LM
Absence of modulation between apolipoprotein E and presenilin 1 genes in Italian families with early-onset Alzheimer's disease
1996-01-01 Nacmias B; Forleo P; Latorraca S; Piacentini S; Amaducci L; Sherrington R; Rogaev E; StGeorgeHyslop P; Rainero I; Pinessi L; Vaula G; Sorbi S
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
Adrenergic regulation of alpha-MSH secretion in man: evidence for a stimulatory role of beta-receptors
1993-01-01 LIMONE P ;D'ALESSANDRO V ;RAINERO I ;AMBROGIO C ;PINESSI L ;DE GENNARO T ;MOLINATTI GM
| 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 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 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 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 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 | |
| Absence of modulation between apolipoprotein E and presenilin 1 genes in Italian families with early-onset Alzheimer's disease | 1996 | Nacmias B; Forleo P; Latorraca S; Piacentini S; Amaducci L; Sherrington R; Rogaev E; StGeorgeHyslop P; Rainero I; Pinessi L; Vaula G; Sorbi S | |
| 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 | |
| Adrenergic regulation of alpha-MSH secretion in man: evidence for a stimulatory role of beta-receptors | 1993 | LIMONE P ;D'ALESSANDRO V ;RAINERO I ;AMBROGIO C ;PINESSI L ;DE GENNARO T ;MOLINATTI GM |