Metzger S;Walter C;Riess O;Roos RA;Nielsen JE;Craufurd D;Nguyen HP;REGISTRY Investigators of the European Huntington’s Disease Network:Bachoud-Lévi AC; Bentivoglio AR; Biunno I; Bonelli RM; Burgunder
JM; Dunnett SB; Ferreira JJ; Handley OJ; Heiberg A; Illmann T; Landwehrmeyer G;
Levey J; Ramos-Arroyo MA; Nielsen J; Koivisto SP; Päivärinta M; Roos RA;
Sebastián AR; Tabrizi S; Vandenberghe W; Verellen-Dumoulin C; Zaremba J; Uhrová
T; Wahlström J; Barth K; Correia-Guedes L; Finisterra AM; Garde MB; Bos R; Betz
S; Callaghan J; Fullam R; Ecker D; Nielsen MG; Handley OJ; Hvalstedt C; Held C;
Koppers K; Laurà M; Horta SM; Descals AM; Díaz MF; Mestre T; Minster S; Monza D; Mütze L; Oehmen M; Townhill J; Orth M; Padieu H; Paterski L; Peppa N; Koivisto
SP; Roedig V; Rialland A; Røren N; Šašinková P; Seliverstov Y; Cubillo PT; van
Walsem MR; Wright A; Silva WV; Witjes-Anné MN; Yudina E; Zielonka D; Zielonka E; Zinzi P; Bonelli RM; Herranhof B; Holl A; Kapfhammer HP; Koppi, The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients., «PLOS ONE», 2013, 8, Article number: e68951 , pp. 1 - 9 [Scientific article]Open Access
Sambati L; Agati R; Bacci A; Bianchi S; Capellari S., Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course., «NEUROLOGICAL SCIENCES», 2013, Neurol Sci. 2013 Jul;34(7):1235-8. doi: 10.1007/s10072-012-1129-3, pp. 1135 - 1138 [Scientific article]
Quarrel O.W.; Handley O.; O'Donovan K.; Dumoulin C.; Ramos-Arroyo M.; Biunno I.; Bauer P.; Kline M.; Capellari S.; Cortelli P.; Gallassi R.; Landwehrmeyer G.B.; European Huntington's Disease Network., Discrepancies in reporting the CAG repeat lengths for Huntington's disease., «EUROPEAN JOURNAL OF HUMAN GENETICS», 2012, 20, pp. 20 - 26 [Scientific article]
Popova S.N.; Tarvainen I.; Capellari S.; Parchi P.; Hannikainen P.; Pirinen E.; Haapasalo H.; Alafuzoff I., Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family., «ACTA NEUROLOGICA SCANDINAVICA», 2012, 126, pp. 315 - 323 [Scientific article]
Martinelli P.; Scaglione C.; Rizzo G.; Capellari S., From Ritual Sword Duel to Electrophysiology: Hyperactive Facial Motor Nucleus in Hemifacial Spasm, «MOVEMENT DISORDERS», 2012, 27, pp. 927 - 928 [Comment or similar]
Jansen C.; Parchi P.; Capellari S.; Ibrahim-Verbaas C.A.; Schuur M.; Strammiello R.; Corrado P.; Bishop M.T.; van Gool W.A.; Verbeek M.M.; Baas F.; van Saane W.; Spliet W.G.; Jansen G.H.; van Duijn C.M.; Rozemuller A.J., Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects., «PLOS ONE», 2012, 7, Article number: e36333 , pp. 1 - 10 [Scientific article]Open Access
Cortelli P.; Terlizzi R.; Capellari S.; Benarroch E., Nuclear lamins: Functions and clinical implications, «NEUROLOGY», 2012, 79, pp. 1726 - 1731 [Scientific article]
Durrenberger P.F.; Fernando F.S.; Magliozzi R.; Kashefi S.N.; Bonnert T.P.; Ferrer I.; Seilhean D.; Nait-Oumesmar B.; Schmitt A.; Gebicke-Haerter P.J.; Falkai P.; Grünblatt E.; Palkovits M.; Parchi P.; Capellari S.; Arzberger T.; Kretzschmar H.; Roncaroli F.; Dexter D.T.; Reynolds R., Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe Study., «ACTA NEUROPATHOLOGICA», 2012, 124, pp. 893 - 903 [Scientific article]
Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; Rozemuller A.J., A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient., «JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY», 2011, 70, pp. 698 - 702 [Scientific article]
G Rizzo; C Tonon; E Malucelli; C Scaglione; C Testa; D Manners; S Capellari; P Cortelli; R Lodi, Abnormal in vivo cerebral energy metabolism in Huntington’s disease: preliminary findings, in: Neurological Sciences, «NEUROLOGICAL SCIENCES», 2011, 32, pp. S268 - S268 (atti di: XLII Congresso Nazionale Società Italiana di Neurologia, Torino, 22-25 October 2011) [Contribution to conference proceedings]
G. Rizzo; C. Tonon; E. Malucelli; C. Scaglione; C. Testa; D. Manners; S. Capellari; R. Lodi; P. Cortelli., Alterazione del metabolismo energetico cerebrale in vivo nella malattia di Huntington: dati preliminari, in: XXXVIII congresso nazionale LIMPE 2011, 2011, pp. 13 - 13 (atti di: XXXVIII congresso nazionale LIMPE 2011, Venezia, Italia, 5-8 Ottobre 2011) [Abstract]
Manners DN; Lodi R; Malucelli E; Testa C; Rizzo G; Capellari S; Pierangeli G; Cortelli P; Montagna P; Barbiroli B; Tonon C; Parchi P, Distribution Of Diffusivity Changes In Subcortical Deep Gray Matter In Prion Diseases, in: 2° Congresso Annuale dell'Italian Chapter dell'ISMRM, 2011, pp. 81 - 81 (atti di: 2° Congresso Annuale dell'Italian Chapter dell'ISMRM, Roma, Italia, 31 marzo-1 aprile 2011) [Abstract]
R Lodi; D N Manners; E Malucelli; C Testa; G Rizzo; S Capellari; R Strammiello; G Pierangeli; P Cortelli; P Montagna; B Barbiroli; C Tonon; P Parchi, Distribution of Diffusivity Changes in Subcortical Deep Gray Matter in Prion Diseases, in: ISMRM 19th Annual Meeting and Exhibition, 2011, pp. 2197 - 2917 (atti di: ISMRM 19th Annual Meeting and Exhibition, Montreal, Canada, 7-13 May 2011) [Abstract]
Marconi S.; Rizzo G.; Capellari S.; Scaglione C.; Cortelli P.; Martinelli P.; Bonazza S., Eating disorder as a psychiatric onset of juvenile Huntington's disease., «THE AMERICAN JOURNAL OF PSYCHIATRY», 2011, 168, pp. 1120 - 1121 [Scientific article]
Parchi P.; Capellari S.; Gambetti P., Fatal Familial and Sporadic Insomnia., in: Esperti Internazionali (N=99), Neurodegeneration:The molecular pathology of dementia and movement disorders., CHICHESTER, Wiley-Blackwell, 2011, pp. 346 - 349 [Chapter or essay]
