Linea 1 - Malattie cerebrovascolari: meccanismi di danno e modelli diagnostico-terapeutici innovativi Amantea D, Bagetta G, Tassorelli C, Mercuri NB, Corasaniti MT. Identification of distinct cellular pools of interleukin-1beta during the evolution of the neuroinflammatory response induced by transient middle cerebral artery occlusion in the brain of rat. Brain Res 2010; 1313:259-69. Panzarasa S, Quaglini S, Sacchi L, Cavallini A, Micieli G, Stefanelli M. Data mining techniques for analyzing stroke care processes.Stud Health Technol Inform 2010; 160(pt 2):939-43 Micieli G, Cavallini A, Quaglini S, Fontana G, Duè M. The Lombardia Stroke Unit Registry: 1-year experience of a web-based hospital stroke registry. Neurol Sci 2010; 31(5):555-64. 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J Immunol Methods 2010;352(1-2):23-31 ol 2009; 16(4):e76-7 Bergamaschi L, Leone MA, Fasano ME, Guerini FR, Ferrante D, Bolognesi E, Barizzone N, Corrado L, Naldi P, Agliardi C, Dametto E, Salvetti M, Visconti A, Galimberti D, Scarpini E, Vercellino M, Bergamaschi R, Monaco F, Caputo D, Momigliano-Richiardi P, D’Alfonso S. HLA-class I markers and multiple sclerosis susceptibility in the Italian population. Genes Immun 2010; 11(2):173-80 Teunissen CE, Tumani H, Bennett J, Berven F, Brundin L, Comabella M, Franciotta D, Federiksen J, Fleming J, Furlan R, Hintzen R, Hughes S, Johnson M, Krasulova E, Kuhle J, Magnone MC, Petzold A, Rajda C, Rejdak K, Schmidt H, Pesch VV, Waubant E, Wolf C, Hemmer B, Deisenhammer F, Giovannoni G. Short commentary on ‘a consensus protocol for the standardization of cerebrospinal fluid collection and biobanking’. Mult Scler 2010; 16(2):129-32 Chiarini M, Sottini A, Ghidini C, Zanotti C, Serana F, Rottoli M, Zaffaroni M, Bergamaschi R, Cordioli C, Capra R, Imberti L. Renewal of the T-cell compartment in multiple sclerosis patients treated with glatiramer acetate. Mult Scler 2010; 16(2):218-27 Patti F, Amato MP, Bastianello S, Caniatti L, Di Monte E, Ferrazza P, Goretti B, Gallo P, Brescia Morra V, Lo Fermo S, Picconi O, Tola M, Trojano M, Effects of immunomodulatory treatment with subcutaneous interferon beta-1a on cognitive decline in mildly disabled patients with relapsing-remitting multiple sclerosis. Mult Scler 2010;16(1):68-77 Delbue S, Tremolada S, Elia F, Carloni C, Amico S, Tavazzi E, Marchioni E, Novati S, Maserati R, Ferrante P. Lymphotropic Polyomavirus is detected in peripheral blood from immunocompromised and healthy subjects. J Clin Virol 2010; 47(2):156-160 Piccolo G, Tavazzi E, Cavallaro T, Romani A, Scelsi R, Martino G. Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. J Neurol Sci 2010; 290(1-2):148-9 Jarius S, Probst C, Borowski K, Franciotta D, Wildemann B, Stoecker W, Wandinger KP. Standardized method for the detection of antibodies to aquaporin-4 based on a highly sensitive immunofluorescence assay employing recombinant target antigen. J Neurol Sci 2010; 291(1-2):52-6 Jarius S, Franciotta D, Bergamaschi R, Wildemann B, Wandinger KP. Immunoglobulin M antibodies to aquaporin-4 in neuromyelitis optica and related disorders. Clin Chem Lab Med 2010; 48(5):659-63 Marchioni E, Tavazzi E, Bastianello S. Non-multiple sclerosis recurrent demyelinating disorders: an ongoing debate. Brain 2010; 133(pt 8):e150 Lolli F, Franciotta D. Oligoclonal bands in tears. Mult Scler 2010; 16(6): 760 Versino M, Biagi F, Bianchi PI, Zardini E, Colnaghi S, Moglia A, Corazza GR, Franciotta D. Gluten sensitivity and the CNS: diagnosis and treatment. Lancet Neurol 2010; 9(7):653; author reply 654-5 Jarius S, Franciotta D, Paul F, Ruprecht K, Bergamaschi R, Rommer PS, Reuss R, Probst C, Kristoferitsch W, Wandinger KP, Wildemann B. Cerebrospinal fluid antibodies to aquaporin-4 in neuromyelitis optica and related disorders: frequency, origin, and diagnostic relevance. J Neuroinflammation 2010; 7: 52 Goretti B, Ghezzi A, Portaccio E, Lori S, Zipoli V, Razzolini L, Moiola L, Falautano M, De Caro MF, Viterbo R, Patti F, Vecchio R, Pozzilli C, Bianchi V, Roscio M, Comi G, Trojano M, Amato MP, (in wich Bergamaschi R, Veggiotti P). Psychosocial issue in children and adolescents with multiple sclerosis. Neurol Sci 2010; 31(4): 467-70 Amato MP, Goretti B, Ghezzi A, Lori S, Zipoli V, Moiola L, Falautano M, De Caro MF, Viterbo R, Patti F, Vecchio R, Pozzilli C, Bianchi V, Roscio M, Martinelli V, Comi G, Portaccio E, Trojano M, (in wich Bergamaschi R, Veggiotti P). Cognitive and psychosocial features in childhood and juvenile MS: two-year follow-up Neurology 2010; 75(13): 1134-40 D’Aguanno S, Franciotta D, Lupisella S, Barassi A, Pieragostino D, Lugaresi A, Centonze D, D’Eril GM, Bernardini S, Federici G, Urbani A. Protein profiling of Guillain-Barrè syndrome cerebrospinal fluid by two-dimensional electrophoresis and mass spectrometry. Neurosci Lett 2010; 485(1):49-54 Tavazzi E, Bargiggia V, Pichiecchio A, Delbue S, Maserati R, Bastianello S, Ferrante P, Minoli L, Ricevuti G, Ceroni M, Marchioni E. HIV-related acute inflammatory leukoencephalopathy of undetermined origin: review of the literature. Int J Immunopathol Pharmacol 2010; 23(3): 693-700 Jarius S, Frederikson J, Waters P, Paul F, Akman-Demir G, Marignier R, Franciotta D, Ruprecht K, Kuenz B, Rommer P, Kristoferitsch W, Wildemann B, Vincent A. Frequency and prognostic impact of antibodies to aquaporin-4 in patients with optic neuritis. J Neurol Sci 2010; 298(1-2):158-62 Absinta M, Rocca MA, Moiola L, Ghezzi A, Milani N, Veggiotti P, Comi G, Filippi M. Brain macro- and microscopic damage in patients with paediatric MS. J Neurol Neurosurg Psychiatry 2010; 81(12):1357-62 Scotti C, Sommi P, Pasquetto MV, Cappelletti D, Stivala S, Mignosi P, Savio M, Chiarelli LR, Valentini G, Bolanos-Garcia VM, Merrell DS, Franchini S, Verona ML, Bolis C, Solcia E, Manca R, Franciotta D, Casasco A, Filipazzi P, Zardini E, Vannini V. Cell-Cycle Inhibition by Helicobacter pylori L-Asparaginase. PLoS One 2010 Linea 3 – Processi neurodegenerativi e disordini del movimento Rosa M, Marceglia S, Servello D, Foffani G, Rossi L, Sassi M, Mrakic-Sposta S, Zangaglia R,Pacchetti C, Porta M, Priori A. Time dependent subthalamic local field potential changes after DBS surgery in Parkinson’s disease. Exp Neurol 2010; 222(2):184-190 Corrado L, Del Bo R, Castellott B, Ratti A, Cereda C, Penco S, Sorarù G, Yari Carlomagno Y, Ghezzi S, Pensato V, Colombrita C, Gagliardi S, Cozzi L, Orsetti V, Mancuso M, Siciliano G, Mazzini L, Comi GP, Gellera C, Ceroni M, D’Alfonso S, Silani V. Mutations of FUS Gene in Sporadic Amyotrophic Lateral Sclerosis Blandini F, Cova L, Armentero MT, Zennaro E, Levandis G, Bossolasco P, Calzarossa C, Mellone M, Giuseppe B, Deliliers GL, Polli E, Nappi G, Silani V. Transplantation of undifferentiated human mesenchymal stem cells protects against 6-hydroxydopamine neurotoxicity in the rat. Cell Transplant 2010; 19(2):203-17 Cova L, Armentero MT, Zennaro E, Calzarossa C, Bossolasco P, Busca G, Deliliers GL, Polli E, Nappi G, Silani V, Blandini F. Multiple neurogenetic and neurorescue effects of human mesenchymal stem cell after transplantation in an experimental model of Parkinson’s disease. Brain Res 2010; 1311:12-27 Zangaglia R, Stocchi F, Sciarretta M, Antonini A, Mancini F, Guidi M, Martignoni E,Pacchetti C. Clinical Experiences With Levodopa Methylester (Melevodopa) in Patients With Parkinson Disease Experiencing Motor Fluctuations: An Open-Label Observational Study. Clin Neuropharmacol 2010; 33(2):61-6 Ambrosi G, Armentero MT, Levandis G, Bramanti P, Nappi G, Blandini F. Effects of early and delayed treatment with an mGluR5 antagonist on motor impairment, nigrostriatal damage and neuroinflammation in a rodent model of Parkinson’s disease. Brain Res Bull 2010; 82(1-2):29-38 Dallocchio C, Arbasino C, Klersy C, Marchioni E. The effects of physical activity on psychogenic movement disorders. Mov Disord 2010; 25(4):421-5 Cova E, Bongioanni P, Cereda C, Metelli MR, Salvaneschi L, Bernuzzi S, Guareschi S, Rossi B, Ceroni M. Time course of oxidant markers and antioxidant defences in subgroups of Amyotrophic lateral Sclerosis patients. Neurochem Int 2010; 56(5):687-693 Colleoni S, Galli C, Giannelli SG, Armentero MT, Blandini F, Broccoli V, Lazzari G. Long-term culture and differentiation of CNS precursors derived from anterior human neural rosettes following exposure to ventralizing factors. Exp Cell Res 2010; 316(7): 1148-58 Terzaghi M, Rustioni V, Manni R, Pacchetti C, Zangaglia R, Ossola M. Agrypnia with nocturnal confusional behaviors in dementia with Lewy bodies: Immediate efficacy of rivastigmine. Mov Disord 2010; 25(5):647-9 Manni R, Terzaghi M, Repetto A, Zangaglia R, Pacchetti C. Complex paroxysmal nocturnal behaviors in Parkinson’s disease. Mov Disord 2010; 25(8): 985-90 Gagliardi S, Cova E, Davin A, Guareschi S, Abel K, Alvisi E, Laforenza U, Ghidoni R, Cashman JR, Ceroni M, Cereda C. SOD1 mRNA expression in sporadic amyotrophic lateral sclerosis. Neurobiol Dis 2010; 39(2):198-203 Battistini S, Ricci C, Lotti EM, Benigni M, Gagliardi S, Zucco R, Bondavalli M, Marcello N,Ceroni M, Cereda C. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. J Neurol Sci 2010; 293(1-2):112-5 Eggert K, Squillacote D, Barone P, Dodel R, Katzenschlager R, Emre M, Lees AJ, Rascol O, Poewe W, Tolosa E, Trenkwalder C, Onofrj M, Stocchi F, Nappi G, Kostic V, Potic J, Ruzicka E, Oertel W. Safety and efficacy of perampanel in advanced Parkinson’s disease: a randomized, placebo-controlled study. Mov Disord 2010; 25(7) Middei S, Roberto A, Berretta N, Panico MB, Lista S, Bernardi G, Mercuri NB, Ammassari-Teule M, Nisticò R. Learning discloses abnormal structural and functional plasticity at hippocampal synapses in the APP23 mouse model of Alzheimer’s disease. Learn Mem 2010;17(5):236-40 Cova E, Ghiroldi A, Guareschi S, Mazzini G, Gagliardi S, Davin A, Bianchi M, Ceroni M,Cereda C. G93A SOD1 alters cell cycle in a cellular model of Amyotrophic Lateral Sclerosis. Cell Signal 2010; 22(10):1477-84 Sinforiani E, Citterio A, Zucchella C, Bono G, Corbetta S, Merlo P, Mauri M. Impact of Gender Differences on the Outcome of Alzheimer’s Disease. Dement Geriatr Cogn Disord 2010; 30(2): 147-54 Blandini F. An update on the potential role of excitotoxicity in the pathogenesis of Parkinson’s disease. Funct Neurol 2010; 25(2): 65 – 71 Cappuccio I, Colapicchioni C, Santangelo V, Sale P, Blandini F, Bonelli M, Niccolini C, Busceti C, Bucci D, Nicoletti F, Melchiorri D. The origin recognition complex subunit, ORC3, is developmentally regulated and supports the expression of biochemical markers of neuronal maturation in cultured cerebellar granule cells. Brain Res 2010; 1358:1-10 Fazi B, Biancolella M, Mehdawy B, Corazzari M, Minella D, Blandini F, Moreno S, Nardacci R, Nisticò R, Sepe S, Novelli G, Piacentini M, Di Sano F. Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain. Neurobiol Dis 2010; 40(3):634-44 Bianchi M, Emanuele E, Davin A, Gagliardi S, Cova E, Meli V, Trotti R, Cereda C. Comparison of three methods for genotyping of prothrombotic polymorphisms. Clin Exp Med 2010; 10(4):269-72 Fumagalli M, Giannicola G, Rosa M, Marceglia S, Lucchiari C, Mrakic-Sposta S, Servello D,Pacchetti C, Porta M, Sassi M, Zangaglia R, Franzini A, Albanese A, Romito L, Piacentini S, Zago S, Pravettoni G, Barbieri S, Priori A. Conflict-dependent dynamic of subthalamic nucleus oscillations during moral decisions. Soc Neurosci 2010; 8:1-14 Albertini V, Bruno A, Paterlini A, Lista S, Benussi L, Cereda C, Binetti G, Ghidoni R. Optimization protocol for amyloid-β peptides detection in human cerebrospinal fluid using SELDI TOF MS. Proteomics Clin Appl 2010; 4(3): 352-7 Fogh I, D’Alfonso S, Gellera C, Ratti A, Cereda C, Penco S, Corrado L, Sorarù G, Castellotti B, Tiloca C, Gagliardi S, Cozzi L, Lupton MK, Ticozzi N, Mazzini L, Shaw CE, Al-Chalabi A, Powell J, Silani V. No association of DPP6 with amyotrophic lateral sclerosis in an Italian population. Neurobiol Aging 2010; doi:10.1016/j.neurobiolaging.2009.05.014 Emanuele E, Lista S, Ghidoni R, Binetti G, Cereda C, Benussi L, Maletta R, Bruni AC, Politi P. Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer’s disease. Neurobiol Aging. 2010; doi:10.1016/j.neurobiolaging.2009.07.003 Armentero MT, Sinforiani E, Ghezzi C, Bazzini E, Levandis G, Ambrosi G, Zangaglia R, Pacchetti C, Cereda C, Cova E, Basso E, Celi D, Martignoni E, Nappi G, Blandini F. Peripheral expression of key regulatory kinases in Alzheimer’s disease and Parkinson’s disease. Neurobiology of Aging 2010; doi:10.1016/j.neurobiolaging.2010.01.004 Ricci C, Battistini S, Cozzi L, Benigni M, Origone P, Verriello L, Lunetta C, Cereda C, Milani P, Greco G, Patrosso MC, Causarano R, Caponnetto C, Giannini F, Corbo M, Penco S. Lack of association of PON polymorphisms with sporadic ALS in an Italian population. Neurobiol Aging 2010; doi:10.1016/j.neurobiolaging.2010.02.010 Corrado L, Carlomagno Y, Falasco L, Mellone S, Godi M, Cova E, Cereda C, Testa L, Mazzini L, D’Alfonso S. A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient. Neurobiol Aging 2010; doi:10.1016/j.neurobiolaging.2010.02.011 Sinforiani E.,Pasotti C.,Chiapella L.,Malinverni P.,Zucchella C.Differences between physician and caregiver evaluations in Alzheimer’s disease. Funct Neurol 2010: 25 (4): 205-9 Linea 4 - Neurologia e psichiatria dello sviluppo Termine C, Trotti R, Ondei P, Gamba G, Montani N, Gamba A, De Simone M, Marni E, Balottin U. Mitral valve prolapse and abnormalities of haemostasis in children and adolescents with migraine with aura and other idiopathic headaches: a pilot study. Acta Neurol Scand 2010; 122(2): 91-6 Ragona F, Brazzo D, Giorgi ID, Morbi M, Freri E, Teutonico F, Gennaro E, Zara F, Binelli S, Veggiotti P, Granata T. Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients. Brain Dev 2010; 32(1):71-7 Veggiotti P, Teutonico F, Alfei E, Nardocci N, Zorzi G, Tagliabue A, De Giorgis V, Balottin U. Glucose transporter type 1 deficiency: Ketogenic diet in three patients with atypical phenotype. Brain Dev 2010; 32(5): 404-8 Ravaglia S, Danesino C, Moglia A, Costa A, Cena H, Maccarini L, Carlucci A, Pichiecchio A, Bini P, De Filippi P, Rossi M. Changes in nutritional status and body composition during enzyme replacement therapy in adult-onset type II glycogenosis. Eur J Neurol 2010; 17(7):957-62 Mercuri E, Clements E, Offiah A, Pichiecchio A, Vasco G, Bianco F, Berardinelli A, Manzur A, Pane M, Messina S, Gualandi F, Ricci E, Rutherford M, Muntoni F. Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine. Ann Neurol 2010 Feb;67(2):201-8 Chiappedi M, Rossi G, Rossi M, Bejor M, Balottin U. Autism and classification systems: a study of 84 children. Ital J Pediatr 2010;36:10 Orcesi S, Tonduti D, Uggetti C, Larizza D, Fazzi E, Balottin U. New case of 4h syndrome and a review of the literature. Pediatr Neurol 2010; 42(5): 359-64 De Filippi P, Ravaglia S, Bembi B, Costa A, Moglia A, Piccolo G, Repetto A, Dardis A, Greco G, Ciana G, Canevari F, Danesino C. The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease. Genet Med 2010; 12(4):206-11 Brun L, Ngu LH, Keng WT, Ch’ng GS, Choy YS, Hwu WL, Lee WT, Willemsen MA, Verbeek MM, Wassenberg T, Régal L, Orcesi S, Tonduti D, Accorsi P, Testard H, Abdenur JE, Tay S, Allen GF, Heales S, Kern I, Kato M, Burlina A, Manegold C, Hoffmann GF, Blau N. Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. Neurology 2010; 75(1):64-71 Guilmatre A, Legallic S, Steel G, Willis A, Di Rosa G, Goldenberg A, Drouin-Garraud V, Guet A, Mignot C, Des Portes V, Valayannopoulos V, Van Maldergem L, Hoffman JD, Izzi C, Espil-Taris C, Orcesi S, Bonafé L, Le Galloudec E, Maurey H, Ioos C, Afenjar A, Blanchet P, Echenne B, Roubertie A, Frebourg T, Valle D, Campion D. Type I hyperprolinemia: genotype/phenotype correlations. Hum Mutat 2010; 31(8):961-5 Verri A, Cremante A, Clerici F, Destefani V, Radicioni A. Klinefelter’s syndrome and psychoneurologic function. Mol Hum Reprod 2010; 16(6):425-33 Messina S, Bruno C, Moroni I, Pegoraro E, D’Amico A, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Farina L, Minetti C, Moggio M, Mongini T, Mottarelli E, Pane M, Pantaleoni C, Pichiecchio A, Pini A, Ricci E, Saredi S, Sframeli M, Tortorella G, Toscano A, Trevisan CP, Uggetti C, Vasco G, Comi GP, Santorelli FM, Bertini E, Mercuri E. Congenital muscular dystrophies with cognitive impairment. A population study. Neurology 2010; 75(10): 898-903 Chiappedi M, Balottin U, Baschenis IM, Piazza F, Bernardi ED, Bejor M. Scientifically based nurture and nature: Alternative but non exclusive hypotheses on attention development. Med Hypotheses 2010; 75(5):445-7 Mazzone E, Martinelli D, Berardinelli A, Messina S, D’Amico A, Vasco G, Main M, Doglio L, Politano L, Cavallaro F, Frosini S, Bello L, Carlesi A, Bonetti AM, Zucchini E, Sanctis RD, Scutifero M, Bianco F, Rossi F, Motta MC, Sacco A, Donati MA, Mongini T, Pini A, Battini R, Pegoraro E, Pane M, Pasquini E, Bruno C, Vita G, Waure CD, Bertini E, Mercuri E. North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy. Neuromuscul Disord 2010; 20(11):712-6 Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D. Four novel cases of periaxin-related neuropathy and review of the literature. Neurology 2010; 75(20): 1830-8 Balbi P, Salvini S, Fundarò C, Frazzitta G, Maestri R, Mosah D, Uggetti C, Sechi G. The clinical spectrum of late-onset Alexander disease: a systematic literature review. J Neurol 2010; 257(12):1955-62 Ravaglia S, Pichiecchio A, Ponzio M, Danesino C, Saeidi Garaghani K, Poloni GU, Toscano A, Moglia A, Carlucci A, Bini P, Ceroni M, Bastianello S. Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response. J Inherit Metab Dis 2010; 33(6):737-45 Rosa-Rizzotto M, Visonà Dalla Pozza L, Turconi AC, Tornetta L, Andreucci E, Zambonin F, Fedrizzi E, Facchin P; Gipci Study Group (in wich Fazzi E, Signorini S). The perception of involved professionals towards research feasibility and usefulness: lessons from the Multi-Site Trial on Efficacy of Constraint Induced Movement Therapy in Children with Hemiplegia. Eur J Phys Rehabil Med. 2010; 46(3): 369-76 Iannicelli M, Brancati F, Mougou-Zerelli S, Mazzotta A, Thomas S, Elkhartoufi N, Travaglini L, Gomes C, Ardissino GL, Bertini E, Boltshauser E, Castorina P, D’Arrigo S, Fischetto R, Leroy B, Loget P, Bonnière M, Starck L, Tantau J, Gentilin B, Majore S, Swistun D, Flori E, Lalatta F, Pantaleoni C, Penzien J, Grammatico P; International JSRD Study Group* (in wich Uggetti C, Signorini S), Dallapiccola B, Gleeson JG, Attie-Bitach T, Valente EM. Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies. Hum Mutat. 2010; 31(5):E1319-31 Linea 5 – Neurologia funzionale e disordini dei comportamenti adattativi Antonaci F, Alfei E, Piazza F, De Cillis I, Balottin U. Therapy-resistant cluster headache in childhood: case report and literature review. Cephalalgia 2010; 30(2): 233-8 Greco R, Gasperi V, Sandrini G, Bagetta G, Nappi G, Maccarrone M, Tassorelli C. 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