Pubblicazioni 2012

 Micieli G, De Falco FA, Consoli D, Inzitari D, Sterzi R, Tedeschi G, Toni D. The role of emergency neurology in Italy: outcome of a consensus meeting for a intersociety position. Neurol Sci 2012; 33(2):297-304

Calabrò RS, Gervasi G, Bramanti P, Cavallini A. Thrombolysis in Ischemic Stroke: Focus on New Treatment Strategies. Recent Pat Cardiovasc Drug Discov 2012; 7(1):42-52

 Bersano A, Lanfranconi S, Valcarenghi C, Bresolin N, Micieli G, Baron P. Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy. Acta Neurol Scand 2012; 126(2):77-97

 Greco R, Amantea D, Mangione AS, Petrelli F, Gentile R, Nappi G, Blandini F, Corasaniti MT, Tassorelli C. Modulation of RAGE Isoforms Expression in the Brain and Plasma of Rats Exposed to Transient Focal Cerebral Ischemia. Neurochem Res 2012; 37(7):1508-16

 Bersano A, Debette S, Zanier ER, Lanfranconi S, De Simoni MG, Zuffardi O, Micieli G. The Genetics of Small-Vessel Disease. Curr Med Chem 2012; 19(24):4124-41

Bersano A, Baron P, Lanfranconi S, Trobia N, Sterzi R, Motto C, Comi G, Sessa M, Martinelli-Boneschi F, Micieli G, Ferrarese C, Santoro P, Parati E, Boncoraglio G, Padovani A, Pezzini A, Candelise L, Candelise L. Lombardia GENS: a collaborative registry for monogenic diseases associated with stroke. Funct Neurol 2012 ; 27(2):107-17

Canova D, Roatta S, Micieli G, Bosone D. Cerebral oxygenation and haemodynamic effectsinduced by nimodipine in healthy subjects.Funct Neurol 2012 ;27(3):169-76

 Cortese A, Baldanti F, Tavazzi E, Carnevale L, Minoli L, Lozza A, Marchioni E. Guillain-Barré syndrome associated with the D222E variant of the 2009 pandemic i+A10:C33nfluenza A (H1N1) virus: Case report and review of the literature. J Neurol Sci 2012; 312 : 173–6

Tavazzi E, White MK, Khalili K. Progressive multifocal leukoencephalopathy: clinical and molecular aspects. Rev Med Virol 2012; 22(1):18-32

Montomoli C, Citterio A, Piccolo G, Cioccale R, Ferretti V, Fratti C, Bergamaschi R, Cosi VE. Epidemiology and geographical variation of myasthenia gravis in the province of Pavia, Italy. Neuroepidemiology 2012; 38(2):100-5

Hughes S, Spelman T, Trojano M, Lugaresi A, Izquierdo G, Grand’maison F, Duquette P, Girard M, Grammond P, Oreja-Guevara C, Hupperts R, Boz C, Bergamaschi R, Giuliani G, Rio ME, Lechner-Scott J, van Pesch V, Iuliano G, Fiol M, Verheul F, Barnett M, Slee M, Herbert J, Kister I, Vella N, Moore F, Petkovska-Boskova T, Shaygannejad V, Jokubaitis V, McDonnell G, Hawkins S, Kee F, Gray O, Butzkueven H. The Kurtzke EDSS rank stability increases 4 years after the onset of multiple sclerosis: results from the MSBase Registry. J Neurol Neurosurg Psychiatry 2012; 83(3):305-10

Pichiecchio A, Tavazzi E, Poloni G, Ponzio M, Palesi F, Pasin M, Piccolo L, Tosello D, Romani A, Bergamaschi R, Piccolo G, Bastianello S. Advanced magnetic resonance imaging of neuromyelitis optica: a multiparametric approach. Mult Scler J 2012; 18(6):817-24

 Meyniel C, Spelman T, Jokubaitis VG, Trojano M, Izquierdo G, Grand’maison F, Oreja-Guevara C, Boz C, Lugaresi A, Girard M, Grammond P, Iuliano G, Fiol M, Cabrera-Gomez JA, Fernandez-Bolanos R, Giuliani G, Lechner-Scott J, Cristiano E, Herbert J, Petkovska-Boskova T, Bergamaschi R, van Pesch V, Moore F, Vella N, Slee M, Santiago V, Barnett M, Havrdova E, Young C, Sirbu CA, Tanner M, Rutherford M, Butzkueven H. Country, Sex, EDSS Change and Therapy Choice Independently Predict Treatment Discontinuation in Multiple Sclerosis and Clinically Isolated Syndrome. PLoS One 2012; 7(6): e38661

 Delbue S, Elia F, Carloni C, Tavazzi E, Marchioni E, Carluccio S, Signorini L, Novati S, Maserati R, Ferrante P. JC virus load in cerebrospinal fluid and transcriptional control region rearrangements may predict the clinical course of progressive multifocal leukoencephalopathy. J Cell Physiol 2012; 227(10):3511-7

 Kister I, Chamot E, Cutter G, Bacon TE, Jokubaitis VG, Hughes SE, Gray OM, Trojano M, Izquierdo G, Grand’maison F, Duquette P, Lugaresi A, Grammond P, Boz C, Hupperts R, Petersen T, Giuliani G, Oreja-Guevara C, Iuliano G, Lechner-Scott J, Bergamaschi R, Rio ME, Verheul F, Fiol M, Van Pesch V, Slee M, Butzkueven H, Herbert J. Increasing age at disability milestones among MS patients in the MSBase Registry. J Neurol Sci 2012; 318(1-2):94-9

Menni C, Lowell WE, Bentzen J, Bergamaschi R, Martinelli Boneschi F, Martinelli V, Bernardinelli L, Stenager E, Davis GE, Foco L.Short and long term variation in ultraviolet radiation and multiple sclerosis. Int J Environ Res Public Health 2012; 9(3): 685-97

 Lechner-Scott J, Spencer B, de Malmanche T, Attia J, Fitzgerald M, Trojano M, Grand’maison F, Antonio C Gomez J, Izquierdo G, Duquette P, Girard M, Grammond P, Oreja-Guevara C, Hupperts R, Bergamaschi R, Boz C, Giuliani G, Pesch VV, Iuliano G, Fiol M, Cristiano E, Verheul F, Saladino ML, Slee M, Barnett M, Deri N, Fletcher S, Vella N, Shaw C, Herbert J, Moore F, Petkovska-Boskova T, Jokubatis V, Butzkueven H. The frequency of CSF oligoclonal banding in multiple sclerosis increases with latitude. Mult Scler 2012; 18(7):974-982

 Jarius S, Franciotta D, Paul F, Bergamaschi R, Rommer PS, Ruprecht K, Ringelstein M, Aktas O, Kristoferitsch W, Wildemann B.Testing for antibodies to human aquaporin-4 by ELISA: Sensitivity, specificity, and direct comparison with immunohistochemistry. J Neurol Sci 2012; 320(1-2):32-7

 Jarius S, Paul F, Franciotta D, de Seze J, Münch C, Salvetti M, Ruprecht K, Liebetrau M, Wandinger K, Akman-Demir G, Melms A, Kristoferitsch W, Wildemann B. Neuromyelitis optica spectrum disorders in patients with myasthenia gravis: ten new aquaporin-4 antibody positive cases and a review of the literature. Mult Scler J 2012; 18(8):1135-43

 Mallucci G, Franciotta D, Romani A, Ceroni M, Bergamaschi R. Anti-aquaporin-4 antibody-positive recurrent isolated optic neuritis and primary Sjögren’s syndrome.J Neurol 2012; 259(8):1740-1

 Di Filippo M, Franciotta D, Massa R, Di Gregorio M, Zardini E, Gastaldi M, Terracciano C, Rastelli E, Gaetani L, Iannone A, Menduno P, Floridi P, Sarchielli P, Calabresi P. Recurrent hyperCKemia with normal muscle biopsy in a pediatric patient with neuromyelitis optica.Neurology 2012 ; 79(11): 1182-4

Pisani V, Stefani A, Pierantozzi M, Natoli S, Stanzione P, Franciotta D, Pisani A. Increased blood-cerebrospinal fluid transfer of albumin in advanced Parkinson’s disease. J Neuroinflammation 2012; 9(–): 188

 Patti F, Amato MP, Trojano M, Bastianello S, Tola MR, Picconi O, Cilia S, Cottone S, Grimaldi LM. Longitudinal changes in social functioning in mildly disabled patients with relapsing-remitting multiple sclerosis receiving subcutaneous interferon -1a: results from the COGIMUS (COGnitive Impairment in MUltiple Sclerosis) study (II). Qual Life Res 202 ; 21(7):1111-21

Zanin V, Delbue S, Marcuzzi A, Tavazzi E, Del Savio R, Crovella S, Marchioni E, Ferrante P, Comar M. Specific protein profile in cerebrospinal fluid from HIV-1-positive cART-treated patients affected by neurological disorders. J Neurovirol 2012; 18 (5): 416-22

Goretti B, Portaccio E, Ghezzi A, Lori S, Moiola L, Falautano M, Viterbo R, Patti F, Vecchio R, Pozzilli C, Bianchi V, Cappiello S, Comi G, Trojano M, Amato MP (in which Bergamaschi R, Veggiotti P). Fatigue and its relationships with cognitive functioning and depression in paediatric multiple sclerosis. Mult Scler 2012; 18(3):329-34

 Grecchi S, Mazzini G, Lisa A, Armentero MT, Bergamaschi R, Romani A, Blandini F, Di Perri C, Scovassi AI. Search for cellular stress biomarkers in lymphocytes from patients with multiple sclerosis: a pilot study. PLoS One 2012; 7(9): e44935

Ferrò MT, Franciotta D, Prelle A, Bestetti A, Cinque P. Active intrathecal herpes simplex virus type 1 (HSV-1) and human herpesvirus-6 (HHV-6) infection at onset of multiple sclerosis. J Neurovirol 2012; 18(5):437-40

 Trojano M, Lucchese G, Graziano G, Taylor BV, Simpson S, Lepore V, Grand’maison F, Duquette P, Izquierdo G, Grammond P, Amato MP, Bergamaschi R, Giuliani G, Boz C, Hupperts R, Van Pesch V, Lechner-Scott J, Cristiano E, Fiol M, Oreja-Guevara C, Saladino ML, Verheul F, Slee M, Paolicelli D, Tortorella C, D’Onghia M, Iaffaldano P, Direnzo V, Butzkueven H. Geographical Variations in Sex Ratio Trends over Time in Multiple Sclerosis. PLoS One ,2012;7(10):e48078

Vairetti M, Ferrigno A, Rizzo V, Ambrosi G, Bianchi A, Richelmi P, Blandini F, Armentero MT. Impaired hepatic function and central dopaminergic denervation in a rodent model of Parkinson’s disease: A self-perpetuating crosstalk? Biochim Biophys Acta 2012; 1822(2):176-84

Melcangi RC, Caruso D, Levandis G, Abbiati F, Armentero MT, Blandini F. Modifications of Neuroactive Steroid Levels in an Experimental Model of Nigrostriatal Degeneration: Potential Relevance to the Pathophysiology of Parkinson’s Disease. J Mol Neurosci 2012; 46(1):177-83

Tiloca C, Ratti A, Pensato V, Castucci A, Sorarù G, Del Bo R, Corrado L, Cereda C, D’Ascenzo C, Comi GP, Mazzini L, Castellotti B, Ticozzi N, Gellera C, Silani V, Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis. Neurobiol Aging 2012; 33(3):630.e1-2

Tassorelli C, Furnari A, Buscone S, Alfonsi E, Pacchetti C, Zangaglia R, Pichiecchio A, Bastianello S, Lozza A, Allena M, Bolla M, Sandrini G, Nappi G, Martignoni E. Pisa syndrome in Parkinson’s disease: Clinical, electromyographic, and radiological characterization. Mov Disord 2012; 27(2):227-35

 Milani P, Gagliardi S, Bongioanni P, Grieco GS, Dezza M, Bianchi M, Cova E, Ceroni M, Cereda C. Effect of the 50bp deletion polymorphism in the SOD1 promoter on SOD1 mRNA levels in Italian ALS patients. J Neurol Sci 2012; 313(1-2):75-8

Cova L, Bossolasco P, Armentero MT, Diana V, Zennaro E, Mellone M, Calzarossa C, Cerri S, Lambertenghi Deliliers G, Polli E, Blandini F, Silani V. Neuroprotective effects of human mesenchymal stem cells on neural cultures exposed to 6-hydroxydopamine: implications for reparative therapy in Parkinson’s disease. Apoptosis 2012; 17(3):289-304

 Blandini F, Armentero MT. New pharmacological avenues for the treatment of l-DOPA-induced dyskinesias in Parkinson’s disease: targeting glutamate and adenosine receptors. Expert Opin Investig Drugs 2012; 21(2):153-68

 Bossolasco P, Cova L, Levandis G, Diana V, Cerri S, Lambertenghi Deliliers G, Polli E, Silani V, Blandini F, Armentero MT. Noninvasive near-infrared live imaging of human adult mesenchymal stem cells transplanted in a rodent model of Parkinson’s disease. Int J Nanomedicine 2012; 7: 435 – 47

 Blandini F, Armentero MT. Animal models of Parkinson’s disease. FEBS J 2012; 279(7):1156-66

 Zucchella C, Bartolo M, Pasotti C, Chiapella L, Sinforiani E. Caregiver Burden and Coping in Early-stage Alzheimer Disease. Alzheimer Dis Assoc Disord 2012; 26(1): 55-60

 Gagliardi S, Ghirmai S, Abel KJ, Lanier M, Gardai SJ, Lee C, Cashman JR. Evaluation in vitro of synthetic curcumins as agents promoting monocytic gene expression related to -amyloid clearance. Chem Res Toxicol 2012; 25(1):101-12

 Guareschi S, Cova E, Cereda C, Ceroni M, Donetti E, Bosco DA, Trotti D, Pasinelli P. An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1. Proc Natl Acad Sci U S A 2012; 109(13):5074-9

 Cashman JR, Gagliardi S, Lanier M, Ghirmai S, Abel KJ, Fiala M. Curcumins Promote Monocytic Gene Expression Related to -Amyloid and Superoxide Dismutase Clearance. Neurodegener Dis 2012; 10(1-4):274-6

 Gagliardi S, Davin A, Ricca I, Grieco GS, Zangaglia R, Pierelli F, Ghiroldi A, Pacchetti C, Casali C, Cereda C. A new GLUT-1 mutation in a family with glucose transporter 1 deficiency syndrome. Mov Disord 2012; 27(6):804-5

 Palesi F, Vitali P, Chiarati P, Castellazzi G, Caverzasi E, Pichiecchio A, Colli-Tibaldi E, D’Amore F, D’Errico I, Sinforiani E, Bastianello S. DTI and MR Volumetry of Hippocampus-PC/PCC Circuit: In Search of Early Micro- and Macrostructural Signs of Alzheimers’s Disease. Neurol Res Int 2012; 2012(–): 517876

 Morelli M, Blandini F, Simola N, Hauser RA. A(2A) Receptor Antagonism and Dyskinesia in Parkinson’s Disease. Parkinsons Dis 2012; 2012(–):489853

 Gagliardi S, Milani P, Sardone V, Pansarasa O, Cereda C. From Transcriptome to Noncoding RNAs: Implications in ALS Mechanism. Neurol Res Int 2012; 2012(–):278725

 Colucci M, Cervio M, Faniglione M, De Angelis S, Pajoro M, Levandis G, Tassorelli C, Blandini F, Feletti F, De Giorgio R, Dellabianca A, Tonini S, Tonini M . Intestinal dysmotility and enteric neurochemical changes in a Parkinson’s disease rat model. Auton Neurosci 2012; 169(2):77-86

 Pisani V, Stefani A, Pierantozzi M, Natoli S, Stanzione P, Franciotta D, Pisani A. Increased blood-cerebrospinal fluid transfer of albumin in advanced Parkinson’s disease. J Neuroinflammation 2012; 9(1):188

 Ratti A, Corrado L, Castellotti B, Del Bo R, Fogh I, Cereda C, Tiloca C, D’Ascenzo C, Bagarotti A, Pensato V, Ranieri M, Gagliardi S, Calini D, Mazzini L, Taroni F, Corti S, Ceroni M, Oggioni GD, Lin K, Powell JF, Sorarù G, Ticozzi N, Comi GP, D’Alfonso S, Gellera C, Silani V.C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. Neurobiol Aging 2012; 33(10):2528.e7-2528.e14

 Giannicola G, Rosa M, Servello D, Menghetti C, Carrabba G, Pacchetti C, Zangaglia R, Cogiamanian F, Scelzo E, Marceglia S, Rossi L, Priori A. Subthalamic Local Field Potentials After Seven-Years Deep Brain Stimulation in Parkinson’s Disease. Exp Neurol 2012; 237(2):312-317

 Mauri M, Sinforiani E, Zucchella C, Cuzzoni MG, Bono G. Progression to dementia in a population with amnestic mild cognitive impairment: clinical variables associated with conversion. Funct Neurol 2012; 27(1):49-54

 Zangaglia R, Pasotti C, Mancini F, Servello D, Sinforiani E, Pacchetti C. Deep brain stimulation and cognition in Parkinson’s disease: An eight-year follow-up study. Mov Disord 2012; 27(9):1192-4

 Tinazzi M, Cipriani A, Matinella A, Cannas A, Solla P, Nicoletti A, Zappia M, Morgante L, Morgante F, Pacchetti C, Sciarretta M, Dallocchio C, Rossi S, Malentacchi M, Ceravolo R, Frosini D, Sestini S, Bovi T, Barbui C. FP-CIT single photon emission computed tomography findings in drug-induced Parkinsonism. Schizophr Res 2012; 139(1-3):40-5

 Sinforiani E, Pasotti C, Chiapella L, Malinverni P, Zucchella C. Memantine in Alzheimer’s disease: experience in an Alzheimer’s disease assessment unit. Aging Clin Exp Res 2012; 24(2):193-6

 Ferrari M, Martignoni E, Blandini F, Riboldazzi G, Bono G, Marino F, Cosentino M. Association of UDP-glucuronosyl transferase 1A9 polymorphisms with adverse reactions to catechol-O-methyltransferase inhibitors in Parkinson’s disease patients. Eur J Clin Pharmacol 2012; 68 (11): 1493-9

 Sinforiani E, Pasotti C, Chiapella L, Picascia M, Zucchella C. Clinical characteristics of population referred to an Italian center for dementia. Aging Clin Exp Res. 2012; 24:104-5

 Zucchella C, Sinforiani E, Citterio A, Giarracca V, Bono G, Mauri M. Reproductive life events and Alzheimer’s disease in Italian women: a retrospective study. Neuropsychiatr Dis Treat 2012; 8(–):555-60

 Nisticò R, Cavallucci V, Piccinin S, Macrì S, Pignatelli M, Mehdawy B, Blandini F, Laviola G, Lauro D, Mercuri NB, D’Amelio M . Insulin Receptor -Subunit Haploinsufficiency Impairs Hippocampal Late-Phase LTP and Recognition Memory. Neuromolecular Med 2012; 14(4):262-9

 Lanni C, Garbin G, Lisa A, Biundo F, Ranzenigo A, Sinforiani E, Cuzzoni G, Govoni S, Ranzani GN, Racchi M. Influence of COMT Val158Met Polymorphism on Alzheimer’s Disease and Mild Cognitive Impairment in Italian Patients. J Alzheimers Dis 2012; 32(4):919-26

 Stanga S, Lanni C, Sinforiani E, Mazzini G, Racchi M. Searching for Predictive Blood Biomarkers: Misfolded p53 in Mild Cognitive Impairment. Curr Alzheimer Res 2012; 9(10):1191-7

Cosentino M, Blandini F, Armentero MT, Martignoni ES, Nappi G, Lecchini S, Marino F. The neurotoxins rotenone, paraquat and manganese exert different effects on human isolated Lymphocites. J Pharmaceutical Sciences and Research 2012; Vol.4(2): 1697-702

 Sassi M, Zekaj E, Grotta A, Pollini A, Pellanda A, Borroni M, Pacchetti C, Menghetti C, Porta M, Servello D. Safety in the Use of Dexmedetomidine (Precedex) for Deep Brain Stimulation Surgery: Our Experience in 23 Randomized Patients. Neuromodulation 2012

 Chiappedi M, Maffioletti E, Piazza F, D’Adda N, Tamburini M, Balottin U. Abilities of preschoolers: comparing different tools. Ital J Pediatr 2012; 38(1):3

 Izzotti A, Longobardi M, Cartiglia C, Anzuini F, Arrigo P, Fazzi E, Orcesi S, La Piana R, Pulliero A. Different Mutations in Three Prime Repair Exonuclease 1 and Ribonuclease H2 Genes Affect Clinical Features in Aicardi-Goutieres Syndrome. J Child Neurol 2012; 27(1):51-60

 Fusar-Poli P, Hobson R, Raduelli M, Balottin U. Reliability and Validity of the Comprehensive Assessment of the at Risk Mental State, Italian Version (CAARMS-I). Curr Pharm Des 2012; 18(4):386-91

 Olivieri I, Bova SM, Urgesi C, Ariaudo G, Perotto E, Fazzi E, Stronati M, Fabbro F, Balottin U, Orcesi S. Outcome of extremely low birth weight infants: What’s new in the third millennium? Neuropsychological profiles at four years. Early Hum Dev 2012; 88(4):241-50

 Tagliabue A, Bertoli S, Trentani C, Borrelli P, Veggiotti P. Effects of the ketogenic diet on nutritional status, resting energy expenditure, and substrate oxidation in patients with medically refractory epilepsy: A 6-month prospective observational study. Clin Nutr 2012; 31(2):246-9

 Fusar-Poli P, Rubia K, Rossi G, Sartori G, Balottin U. Striatal Dopamine Transporter Alterations in ADHD: Pathophysiology or Adaptation to Psychostimulants? A Meta-Analysis. Am J Psychiatry 2012; 169(3):264-72

Pulliero A, Marengo B, Domenicotti C, Longobardi MG, Fazzi E, Orcesi S, Bianchi M, Balottin U, Izzotti A. Inhibition of neuroblastoma cell growth by TREX1-mutated human lymphocytes. Oncol Rep 2012; 27(5):1689-94

 Balottin U, Calcaterra E, Zambonin F, Veggiotti P, Luoni C, Termine C. Chorea mollis: long-term follow-up of an infantile case. Neurol Sci 2012; 33(3):643-5

 Fazzi E, Signorini SG, LA Piana R, Bertone C, Misefari W, Galli J, Balottin U, Bianchi PE. Neuro-ophthalmological disorders in cerebral palsy: ophthalmological, oculomotor, and visual aspects. Dev Med Child Neurol 2012; 54(8):730-6

 Bello L, Piva L, Barp A, Taglia A, Picillo E, Vasco G, Pane M, Previtali SC, Torrente Y, Gazzerro E, Motta MC, Grieco GS, Napolitano S, Magri F, D’Amico A, Astrea G, Messina S, Sframeli M, Vita GL, Boffi P, Mongini T, Ferlini A, Gualandi F, Soraru’ G, Ermani M, Vita G, Battini R, Bertini E, Comi GP, Berardinelli A, Minetti C, Bruno C, Mercuri E, Politano L, Angelini C, Hoffman EP, Pegoraro E. Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology 2012; 79(2):159-62

 Signorini SG, Decio A, Fedeli C, Luparia A, Antonini M, Bertone C, Misefari W, Ruberto G, Bianchi PE, Balottin U. Septo-optic dysplasia in childhood: the neurological, cognitive and neuro-ophthalmological perspective. Dev Med Child Neurol 2012; 54(11):1018-24

 Orcesi S, Olivieri I, Longo S, Perotti G, La Piana R, Tinelli C, Spinillo A, Balottin U, Stronati M. Neurodevelopmental outcome of preterm very low birth weight infants born from 2005 to 2007. Eur J Paediatr Neurol 2012; 16(6):716-23

 Tonduti D, Pichiecchio A, La Piana R, Livingston JH, Doherty DA, Majumdar A, Tomkins S, Mine M, Ceroni M, Ricca I, Balottin U, Orcesi S. COL4A1-Related Disease: Raised Creatine Kinase and Cerebral Calcification as Useful Pointers. Neuropediatrics 2012; 43(5):283-8

 Chiappedi M, Togni R, De Bernardi E, Baschenis IM, Battezzato S, Balottin U, Toffola ED, Bejor M. rm trajectories and writing strategy in healthy children. BMC Pediatr 2012; 12(1):173

 Cavanna AE, Selvini C, Termine C, Balottin U, Eddy CM. Tolerability profile of clonidine in the treatment of adults with tourette syndrome. Clin Neuropharmacol 2012; 35(6):269-72

 Schmidt JL, Olivieri I, Vento JM, Fazzi E, Gordish-Dressman H, Orcesi S, Vanderver A. Family history of autoimmune disease in patients with aicardi-goutières syndrome. Clin Dev Immunol 2012; 2012(–):206730

 Muratori F, Tancredi R, Massagli A, Esposito D, Villa L, Valli A, Molteni M, Militerni R, Frolli A, Balottin U, Carigi T, Gallo ML, Giuberti V, Pitanti V, Germelli C, Giorgi A, Vannucchi L, Armellini M, Campanile S, Casella C, Monti A, Masini S, Pini G, Calugi S, A. Narzisi A. Effetti a sei mesi dell’intervento precoce nei disturbi dello spettro autistico. Gior Neuropsich Età Evol 2012; 32:135-50

 Pane M, Lombardo ME, Alfieri P, D’Amico A, Bianco F, Vasco G, Piccini G, Mallardi M, Romeo DM, Ricotti V, Ferlini A, Gualandi F, Vicari S, Bertini E, Berardinelli A, Mercuri E. Attention Deficit Hyperactivity Disorder and Cognitive Function in Duchenne Muscular Dystrophy: Phenotype-Genotype Correlation. J Pediatr 2012; 22(8):685-9

 Pane M, Messina S, Vasco G, Foley AR, Morandi L, Pegoraro E, Mongini T, D’Amico A, Bianco F, Lombardo ME, Scalise R, Bruno C, Berardinelli A, Pini A, Moroni I, Mora M, Toscano A, Moggio M, Comi G, Santorelli FM, Bertini E, Muntoni F, Mercuri E. Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency. Neuromuscul Disord 2012; 22(8):685-9

 Estrada-Cuzcano A, Koenekoop RK, Senechal A, De Baere EB, de Ravel T, Banfi S, Kohl S, Ayuso C, Sharon D, Hoyng CB, Hamel CP, Leroy BP, Ziviello C, Lopez I, Bazinet A, Wissinger B, Sliesoraityte I, Avila-Fernandez A, Littink KW, Vingolo EM, Signorini S, Banin E, Mizrahi-Meissonnier L, Zrenner E, Kellner U, Collin RW, den Hollander AI, Cremers FP, Klevering BJ. BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome. Arch Ophthalmol 2012;130(11): 1425-32

 Scionti I, Greco F, Ricci G, Govi M, Arashiro P, Vercelli L, Berardinelli A, Angelini C, Antonini G, Cao M, Di Muzio A, Moggio M, Morandi L, Ricci E, Rodolico C, Ruggiero L, Santoro L, Siciliano G, Tomelleri G, Trevisan CP, Galluzzi G, Wright W, Zatz M, Tupler R. Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy. Am J Hum Genet 2012; 90(4): 628-35

Terrazzino S, Tassorelli C, Sances G, Allena M, Viana M, Monaco F, Bellomo G, Nappi G, Canonico PL, Genazzani AA. Association of haplotype combination of serotonin transporter gene polymorphisms with monthly headache days in MOH patients. Eur J Neurol 2012; 19(1): 69-75

 Berliocchi L, Russo R, Tassorelli C, Morrone LA, Bagetta G, Corasaniti MT. Death in pain: peripheral nerve injury and spinal neurodegenerative mechanisms. Curr Opin Pharmacol 2012; 12(1):49-54

 Linde M, Gustavsson A, Stovner LJ, Steiner TJ, Barré J, Katsarava Z, Lainez JM, Lampl C, Lantéri-Minet M, Rastenyte D, Ruiz de la Torre E, Tassorelli C, Andrée C. The cost of headache disorders in Europe: the Eurolight project. Eur J Neurol 2012; 19(5):703-711

Nappi RE, Terreno E, Tassorelli C, Sances G, Allena M, Guaschino E, Antonaci F, Albani F, Polatti F . Sexual Function and Distress in Women Treated for Primary Headaches in a Tertiary University Center. J Sex Med 2012; 9(3):761-769

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 Salviati L, Trevisson E, Rodriguez Hernandez MA, Casarin A, Pertegato V, Doimo M, Cassina M, Agosto C, Desbats MA, Sartori G, Sacconi S, Memo L, Zuffardi O, Artuch R, Quinzii C. Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. J Med Genet 2012; 49(3):187-91

 Vetro A, Bouman K, Hastings R, McMullan DJ, Vermeesch JR, Miller K, Sikkema-Raddatz B, Ledbetter DH, Zuffardi O, van Ravenswaaij-Arts CM . The introduction of arrays in prenatal diagnosis: A special challenge. Hum Mutat 2012; 33(6):923-9

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 Rossi E, Giorda R, Bonaglia MC, Candia SD, Grechi E, Franzese A, Soli F, Rivieri F, Patricelli MG, Saccilotto D, Bonfante A, Giglio S, Beri S, Rocchi M, Zuffardi O. De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s. PLoS One. 2012; 7(6):e39180

 Di Lorenzo C, Di Lorenzo G, Daverio A, Pasqualetti P, Coppola G, Giannoudas I, Barone Y, Grieco GS, Niolu C, Pascale E, Santorelli FM, Nicoletti F, Pierelli F, Siracusano A, Seri S. The Val66Met Polymorphism of the BDNF Gene Influences Trigeminal Pain-Related Evoked Responses. J Pain 2012; 13(9):866-73

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