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219 results

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Page 1
Red flags for multiple system atrophy.
Köllensperger M, Geser F, Seppi K, Stampfer-Kountchev M, Sawires M, Scherfler C, Boesch S, Mueller J, Koukouni V, Quinn N, Pellecchia MT, Barone P, Schimke N, Dodel R, Oertel W, Dupont E, Østergaard K, Daniels C, Deuschl G, Gurevich T, Giladi N, Coelho M, Sampaio C, Nilsson C, Widner H, Sorbo FD, Albanese A, Cardozo A, Tolosa E, Abele M, Klockgether T, Kamm C, Gasser T, Djaldetti R, Colosimo C, Meco G, Schrag A, Poewe W, Wenning GK; European MSA Study Group. Köllensperger M, et al. Among authors: pellecchia mt. Mov Disord. 2008 Jun 15;23(8):1093-9. doi: 10.1002/mds.21992. Mov Disord. 2008. PMID: 18442131
Paroxysmal dystonia in Behçet's disease.
Pellecchia MT, Cuomo T, Striano S, Filla A, Barone P. Pellecchia MT, et al. Mov Disord. 1999 Jan;14(1):177-9. doi: 10.1002/1531-8257(199901)14:1<177::aid-mds1037>3.0.co;2-n. Mov Disord. 1999. PMID: 9918371 No abstract available.
Brain stem cystic astrocytoma presenting with "pure" parkinsonism.
Cicarelli G, Pellecchia MT, Maiuri F, Barone P. Cicarelli G, et al. Among authors: pellecchia mt. Mov Disord. 1999 Mar;14(2):364-6. doi: 10.1002/1531-8257(199903)14:2<364::aid-mds1028>3.0.co;2-i. Mov Disord. 1999. PMID: 10091637 No abstract available.
Possible gluten sensitivity in multiple system atrophy.
Pellecchia MT, Ambrosio G, Salvatore E, Vitale C, De Michele G, Barone P. Pellecchia MT, et al. Neurology. 2002 Oct 8;59(7):1114-5. doi: 10.1212/wnl.59.7.1114. Neurology. 2002. PMID: 12370481 No abstract available.
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T; European Multiple System Atrophy Study Group. Kamm C, et al. Among authors: pellecchia mt. Brain. 2005 Aug;128(Pt 8):1855-60. doi: 10.1093/brain/awh535. Epub 2005 Jun 9. Brain. 2005. PMID: 15947063
UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.
Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Pellecchia MT, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW; European MSA Study Group. Healy DG, et al. Among authors: pellecchia mt. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636
219 results