Pubblicazioni 2010

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.

Petzold A, Altintas A, Andreoni L, Bartos A, Berthele A, Blankenstein MA, Buee L, Castellazzi M, Cepok S, Comabella M, Constantinescu CS, Deisenhammer F, Deniz G, Erten G, Espiño M, Fainardi E, Franciotta D, Freedman M, Giedraitis V, Gilhus NE, Giovannoni G, Glabinski A, Grieb P, Hartung HP, Hemmer B, Herukka SK, Hintzen R, Ingelsson M, Jackson S, Jacobsen S, Jafari N, Jalosinski M, Jarius S, Kapaki E, Kieseier BC, Koel-Simmelink MJ, Kornhuber J, Kuhle J, Kurzepa J, Lalive P, Lannfelt L, Lehmensiek V, Lewczuk P, Livrea P, Marnetto F, Martino D, Menge T, Norgren N, Papuc E, Paraskevas GP, Pirttilä T, Rajda C, Rejdak K, Ricny J, Ripova D, Rosengren L, Ruggieri M, Schraen S, Shaw G, Sindic C, Siva A, Stigbrand T, Stonebridge I, Topcular B, Trojano M, Tumani H, Twaalfhoven HA, Vécsei L, Van Pesch V, Vanderstichele H, Vedeler C, Verbeek MM, Villar LM, Weissert R, Wildemann B, Yang C, Yao K, Teunissen C. Neurofilament ELISA validation. 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

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

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

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. Alterations of the endocannabinoid system in an animal model of migraine: evaluation in cerebral areas of rat. Cephalalgia 2010; 30(3) 296-302

Perrotta A, Serrao M, Sandrini G, Burstein R, Sances G, Rossi P, Bartolo M, Pierelli F, Nappi G. Sensitisation of spinal cord pain processing in medication overuse headache involves supraspinal pain control. Cephalalgia 2010; 30(3) 272-84

Sances G, Ghiotto N, Galli F, Guaschino E, Rezzani C, Guidetti V, Nappi G. Risk factors in medication-overuse headache: a 1-year follow-up study (CARE II protocol). Cephalalgia 2010; 30(3) 329-36

Versino M, Newman-Toker DE. Blind spot heterotopia by automated static perimetry to assess static ocular torsion: centro-cecal axis rotation in normals. J Neurol 2010; 257(2):291-3

Sances G, Galli F, Anastasi S, Ghiotto N, De Giorgio G, Guidetti V, Firenze C, Pazzi S, Quartesan R, Gallucci M, Nappi G. Medication-Overuse Headache and Personality: A Controlled Study by Means of the MMPI-2 Headache 2010; 50(2):198-209

Antonaci F, Dumitrache C, De Cillis I, Allena M. A review of current European treatment guidelines for migraine. J Headache Pain 2010; 11(1):13-9

Rossi P, Tassorelli C, Allena M, Ferrante E, Lisotto C, Nappi G. Focus on therapy: Hemicrania continua and new daily persistent headache. J Headache Pain 2010; 11(3):259-65

Antonaci F, Allena M, De Cillis I, Montagna P, Savi L. Linee Guida Europee per il trattamento delle forme più comuni di cefalea nella medicina generale. Minerva Med 2010; 101 (Suppl. 2 al N. 1):1-19

Ferrante E, Rossi P, Tassorelli C, Lisotto C, Nappi G. Focus on therapy of primary stabbing headache. J Headache Pain 2010; 11(2):157-60

Termine C, Ferri M, Livetti G, Beghi E, Salini S, Mongelli A, Blangiardo R, Luoni C, Lanzi G,Balottin U. Migraine with aura with onset in childhood and adolescence: Long-term natural history and prognostic factors. Cephalalgia 2010; 30(6):674-81

Lisotto C, Rossi P, Tassorelli C, Ferrante E, Nappi G. Focus on therapy of hypnic headache. J Headache Pain 2010; 11(4):349-54

Antonaci F, De Cillis I, Cuzzoni MG, Allena M. Almotriptan for the treatment of acute migraine: a review of early intervention trials. Expert Rev Neurother 2010; 10(3):351-64

Mangiacavalli S, Corso A, De Amici M, Varettoni M, Alfonsi E, Lozza A, Lazzarino M. Emergent T-helper 2 profile with high interleukin-6 levels correlates with the appearance of bortezomib-induced neuropathic pain. Br J Haematol 2010; 149(6): 916-8

Terzaghi M, Ghiotto N, Sances G, Rustioni V, Nappi G, Manni R. Episodic Cluster Headache: NREM Prevalence of Nocturnal Attacks. Time to Look Beyond Macrostructural Analysis? Headache 2010; 50(6):1050-4

Greco R, Gasperi V, Maccarrone M, Tassorelli C. The endocannabinoid system and migraine. Exp Neurol 2010; 224(1):85-91

Terrazzino S, Viana M, Floriddia E, Monaco F, Mittino D, Sances G, Tassorelli C, Nappi G, Rinaldi M, Canonico PL, Genazzani AA. The serotonin transporter gene polymorphism STin2 VNTR confers an increased risk of inconsistent response to triptans in migraine patients. Eur J Pharmacol 2010; 641(2-3):82-7

Allena M, Tassorelli C, Sances G, Guaschino E, Sandrini G, Nappi G, Antonaci F. Is Hemicrania Continua a Single Entity or the Association of Two Headache Forms? Considerations From a Case Report. Headache Headache 2010; 50(5):877-81

Antonaci F, Sances G, Loi M, Sandrini G, Dumitrache C, Cuzzoni MG. SUNCT syndrome with paroxysmal mydriasis: Clinical and pupillometric findings. Cephalalgia 2010; 30(8): 987-90

Andrée C, Vaillant M, Barre J, Katsarava Z, Lainez JM, Lair ML, Lanteri-Minet M, Lampl C, Steiner TJ, Stovner LJ, Tassorelli C, Sándor PS. Development and validation of the EUROLIGHT questionnaire to evaluate the burden of primary headache disorders in Europe. Cephalalgia 2010; 30(9):1082-100

Bendtsen L, Evers S, Linde M, Mitsikostas DD, Sandrini G, Schoenen J. EFNS guideline on the treatment of tension-type headache – Report of an EFNS task force. Eur J Neurol 2010; 17(11):1318-25

Terrazzino S, Sances G, Balsamo F, Viana M, Monaco F, Bellomo G, Martignoni E,Tassorelli C, Nappi G, Canonico PL, Genazzani AA. Role of 2 Common Variants of 5HT2A Gene in Medication Overuse Headache. Headache 2010; 50(10):1587-96

De Carlo D, Dal Zotto L, Perissinotto E, Gallo L, Gatta M, Balottin U, Mazzotta G, Moscato D, Raieli V, Rossi LN, Sangermani R, Soriani S, Termine C, Tozzi E, Vecchio A, Zanchin G, Battistella P. Osmophobia in migraine classification: A multicentric study in juvenile patients. Cephalalgia 2010; 30(12):1486-94

Allena M, Rossi P, Tassorelli C, Ferrante E, Lisotto C, Nappi G. Focus on therapy of the Chapter IV headaches provoked by exertional factors: primary cough headache, primary exertional headache and primary headache associated with sexual activity. J Headache Pain 2010; 11(6):525-30

Alfonsi E, Merlo IM, Ponzio M, Montomoli C, Tassorelli C, Biancardi C, Lozza A, Martignoni E. An electrophysiological approach to the diagnosis of neurogenic dysphagia; implications for botulinum toxin treatment. J Neurol Neurosurg Psychiatry 2010;81(1):54-60

Bartolo M, Serrao M, Tassorelli C, Don R, Ranavolo A, Draicchio F, Pacchetti C, Buscone S, Perrotta A, Furnari A, Bramanti P, Padua L, Pierelli F, Sandrini G. Four-week trunk-specific rehabilitation treatment improves lateral trunk flexion in Parkinson’s disease. Mov Disord 2010;  25(3):325-31

Luccichenti G, Cademartiri F, Pichiecchio A, Bontempi E, Sabatini U, Bastianello S. User Interface of a Teleradiology System for the MR Assessment of Multiple Sclerosis. J Digit Imaging 2010; 23(5):632-8

Accornero S, Danesino C, Bastianello S, D’Errico I, Guala A, Chiovato L. Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene. J Clin Endocrinol Metab 2010; 95(8): 3595-6

Bartolo M, De Luca D, Serrao M, Sinforiani E, Zucchella C, Sandrini G. Caregivers burden and needs in community neurorehabilitation. J Rehabil Med 2010; 42(9):818-22

Serrao M, Coppola G, Di Lorenzo C, Di Fabio R, Padua L, Sandrini G, Pierelli F. Nociceptive trigeminocervical reflexes in healthy subjects. Clin Neurophysiol 2010;  121(9):1563-68

Giugni E, Vadalà R, Pezzella F R, Luccichenti G, Bastianello S. Imaging not imagination: towards a revision of the role of neuroimaging in the diagnosis of dementia. Funct Neurol 2010; 25(2): 61-3

Maccabelli G, Pichiecchio A, Guala A, Ponzio M, Palesi F, Maranzana Rt D, Poloni GU, Bastianello S, Danesino C. Advanced magnetic resonance imaging in benign hereditary chorea: Study of two familial cases. Mov Disord 2010; 15; 25(15):2670-4

Pezzella M, Yeghiazaryan NS, Veggiotti P, Bettinelli A, Giudizioso G, Zara F, Striano P, Minetti C. Galloway-Mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature. Seizure 2010; 19(2):132-5

Alexandre V, Capovilla G, Fattore C, Franco V, Gambardella A, Guerrini R, La Briola F, Ladogana M, Rosati E, Specchio LM, Striano S, Perucca E. Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy. Epilepsia 2010; 51(5):921-5

Saetre E, Abdelnoor M, Perucca E, Taubøll E, Isojärvi J, Gjerstad L. Antiepileptic drugs and quality of life in the elderly: Results from a randomized double-blind trial of carbamazepine and lamotrigine in patients with onset of epilepsy in old age. Epilepsy Behav 2010; 17(3):395-401

Arzimanoglou A, Ryvlin P, Perucca E. When the past challenges the present: are older antiepileptic drugs still the best choice in childhood absence epilepsy? Lancet Neurol 2010; 9(5):457-9

Ossola M, Romani A, Tavazzi E, Pichiecchio A, Galimberti CA. Epileptic mechanisms in Charles Bonnet syndrome. Epilepsy Behav 2010; 18(1-2):119-22

Perucca E. When clinical trials make history: Demonstrating efficacy of new antiepileptic drugs as monotherapy. Epilepsia 2010; 51(10):1933-5

Rheims S, Perucca E, Ryvlin P. Placebo-corrected efficacy of modern antiepileptic drugs for refractory epilepsy: Reply to Beyenburg et al., 2009. Epilepsia 2010; 51(5): 935-6

Canevini MP, De Sarro G, Galimberti CA, Gatti G, Licchetta L, Malerba A, Muscas G, La Neve A, Striano P, Perucca E. Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug-refractory epilepsy. Epilepsia 2010; 51(5):797-804

Manni R, Terzaghi M. Comorbidity between epilepsy and sleep disorders. Epilepsy Res 2010; 90(3):171-7

Moshel YA, Elliott R, Teutonico F, Sellin J, Carlson C, Devinsky O, Weiner HL. Do tubers contain function? Resection of epileptogenic foci in perirolandic cortex in children with tuberous sclerosis complex. Epilepsia 2010; 51(7):1242-51

Perucca P, Terzaghi M, Manni R. Status epilepticus migrainosus: clinical, electrophysiologic, and imaging characteristics. Neurology 2010; 75(4):373-4

Olivieri I, Teutonico F, Orcesi S, Papalia G, Uggetti C, Bastianello S, Balottin U, Veggiotti P. Paroxysmal tonic eye deviation: an atypical presentation of hypothalamic hamartoma. Epileptic Disord 2010;  12(3):233-5

Yeghiazaryan NS, Morana G, Veggiotti P, Savino G, Minetti C, Rossi A, Striano P, Giordano L. Temporal lobe epilepsy and hippocampal malrotation: Is there a causal association?Epilepsy Behav 2010; 18(4):502-4

Malerba A, Ciampa C, De Fazio S, Fattore C, Frassine B, La Neve A, Pellacani S, Specchio LM, Tiberti A, Tinuper P, Perucca E. Patterns of prescription of antiepileptic drugs in patients with refractory epilepsy at tertiary referral centres in Italy. Epilepsy Res 2010; 91(2-3): 273-82

Coppola G, Grosso S, Franzoni E, Veggiotti P, Zamponi N, Parisi P, Spalice A, Habetswallner F, Fels A, Capovilla G, Verrotti A, Mangano S, Balestri A, Curatolo P, Pascotto A.Rufinamide in children and adults with Lennox-Gastaut syndrome: First Italian multicenter experience. Seizure 2010; 19(9):587-91

Piccinelli P, Beghi E, Borgatti R, Ferri M, Giordano L, Romeo A, Termine C, Viri M, Zucca C, Balottin U. Neuropsychological and behavioural aspects in children and adolescents with idiopathic epilepsy at diagnosis and after 12 months of treatment. Seizure 2010; 19(9):540-6

Bialer M, Johannessen SI, Levy RH, Perucca E, Tomson T, White HS. Progress report on new antiepileptic drugs: A summary of the Tenth Eilat Conference (EILAT X). Epilepsy Res 2010; 92(2-3):89-124

Mapelli J, Gandolfi D, D’Angelo E. Combinatorial responses controlled by synaptic inhibition in the cerebellum granular layer. J Neurophysiol 2010; 103(1):250-61

D’Angelo E. Homeostasis of intrinsic excitability: making the point. J Physiol 2010; 588(Pt 6):901-2

Arleo A, Nieus T, Bezzi M, D’Errico A, D’Angelo E, Coenen OJ. How Synaptic Release Probability Shapes Neuronal Transmission: Information-Theoretic Analysis in a Cerebellar Granule Cell. Neural Comput 2010; 22(8):2031-58

Solinas S, Nieus T, D’Angelo E. A realistic large-scale model of the cerebellum granular layer predicts circuit spatio-temporal filtering properties. Front Cell Neurosci 2010; 4:12

Boso M, Emanuele E, Prestori F, Politi P, Barale F, D’Angelo E. Autism and genius: is there a link? The involvement of central brain loops and hypotheses for functional testing. The involvement of central brain loops and hypotheses for functional testing. Funct Neurol 2010; 25 (1):15-20

Galliano E, Mazzarello P, D’Angelo E. Discovery and rediscoveries of Golgi cells. J Physiol 2010; 588(Pt 19):3639-55

Giza J, Urbanski MJ, Prestori F, Bandyopadhyay B, Yam A, Friedrich V, Kelley K, D’Angelo E, Goldfarb M. Behavioral and cerebellar transmission deficits in mice lacking the autism-linked gene islet brain-2.  J Neurosci 201030 (44):14805-16

Mapelli J, Gandolfi D, D’Angelo E. High-Pass Filtering and Dynamic Gain Regulation Enhance Vertical Bursts Transmission along the Mossy Fiber Pathway of Cerebellum. Front Cell Neurosci 2010; 4:14

Dover K, Solinas S, D’Angelo E, Goldfarb M. Long-term inactivation particle for voltage-gated sodium channels. J Physiol 2010; 588(Pt 19):3695-711

van Bon BW, Koolen DA, Brueton L, McMullan D, Lichtenbelt KD, Adès LC, Peters G, Gibson K, Novara F, Pramparo T, Bernardina BD, Zoccante L, Balottin U, Piazza F, Pecile V, Gasparini P, Guerci V, Kets M, Pfundt R, de Brouwer AP, Veltman JA, de Leeuw N, Wilson M, Antony J, Reitano S, Luciano D, Fichera M, Romano C, Brunner HG, Zuffardi O, de Vries BB. The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. Eur J Hum Genet 2010; 18(2):163-70

Gimelli S, Chrast J, Baban A, Henrichsen CN, Lerone M, Zuffardi O, Gimelli G, Reymond A. A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromes. Am J Med Genet A 2010; 152A(5):1285-94

Lindstrand A, Malmgren H, Verri A, Benetti E, Eriksson M, Nordgren A, Anderlid BM, Golovleva I, Schoumans J, Blennow E. Molecular and clinical characterization of patients with overlapping 10p deletions. Am J Med Genet A 2010; 152A(5):1233-43

Novara F, Beri S, Giorda R, Ortibus E, Nageshappa S, Darra F, Bernardina BD, Zuffardi O, Van Esch H. Refining the phenotype associated with MEF2C haploinsufficiency. Clin Genet 2010; 78(5):471-7

Bonaglia MC, Marelli S, Novara F, Commodaro S, Borgatti R, Minardo G, Memo L, Mangold E, Beri S, Zucca C, Brambilla D, Molteni M, Giorda R, Weber RG, Zuffardi O. Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions. Eur J Hum Genet 2010; 18(12):1302-9