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Page 1
CTA/CTG expansions at the SCA 8 locus in multiple system atrophy.
Munhoz RP, Teive HA, Raskin S, Werneck LC. Munhoz RP, et al. Among authors: raskin s. Clin Neurol Neurosurg. 2009 Feb;111(2):208-10. doi: 10.1016/j.clineuro.2008.09.003. Epub 2008 Nov 5. Clin Neurol Neurosurg. 2009. PMID: 18980793
Rigid spine syndrome. Case report.
Zétola VH, Scola RH, Raskin S, Prevendello DM, Correa Neto Y, Werneck LC. Zétola VH, et al. Among authors: raskin s. Arq Neuropsiquiatr. 1998 Dec;56(4):812-8. doi: 10.1590/s0004-282x1998000500018. Arq Neuropsiquiatr. 1998. PMID: 10029887
Huntington disease: DNA analysis in Brazilian population.
Raskin S, Allan N, Teive HA, Cardoso F, Haddad MS, Levi G, Boy R, Lerena Junior J, Sotomaior VS, Janzen-Dück M, Jardim LB, Fellander FR, Andrade LA. Raskin S, et al. Arq Neuropsiquiatr. 2000 Dec;58(4):977-85. doi: 10.1590/s0004-282x2000000600001. Arq Neuropsiquiatr. 2000. PMID: 11105061 Free article.
Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease.
Rawal N, Periquet M, Dürr A, de Michele G, Bonifati V, Teive HA, Raskin S, Guimaraes J, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Rawal N, et al. Among authors: raskin s. J Neurol. 2002 Aug;249(8):1127-9. doi: 10.1007/s00415-002-0757-6. J Neurol. 2002. PMID: 12420720 No abstract available.
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism.
Rawal N, Periquet M, Lohmann E, Lücking CB, Teive HA, Ambrosio G, Raskin S, Lincoln S, Hattori N, Guimaraes J, Horstink MW, Dos Santos Bele W, Brousolle E, Destée A, Mizuno Y, Farrer M, Deleuze JF, De Michele G, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Rawal N, et al. Among authors: raskin s. Neurology. 2003 Apr 22;60(8):1378-81. doi: 10.1212/01.wnl.0000056167.89221.be. Neurology. 2003. PMID: 12707451
Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Periquet M, et al. Among authors: raskin s. Brain. 2003 Jun;126(Pt 6):1271-8. doi: 10.1093/brain/awg136. Brain. 2003. PMID: 12764050
How much phenotypic variation can be attributed to parkin genotype?
Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destée A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Lohmann E, et al. Among authors: raskin s. Ann Neurol. 2003 Aug;54(2):176-85. doi: 10.1002/ana.10613. Ann Neurol. 2003. PMID: 12891670
345 results