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Olfactory heterogeneity in LRRK2 related Parkinsonism.
Silveira-Moriyama L, Munhoz RP, de J Carvalho M, Raskin S, Rogaeva E, de C Aguiar P, Bressan RA, Felicio AC, Barsottini OG, Andrade LA, Chien HF, Bonifati V, Barbosa ER, Teive HA, Lees AJ. Silveira-Moriyama L, et al. Among authors: raskin s. Mov Disord. 2010 Dec 15;25(16):2879-83. doi: 10.1002/mds.23325. Mov Disord. 2010. PMID: 20818658
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.
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
Atypical parkinsonism and SCA8.
Munhoz RP, Teive HA, Raskin S, Troiano AR. Munhoz RP, et al. Among authors: raskin s. Parkinsonism Relat Disord. 2006 Apr;12(3):191-2. doi: 10.1016/j.parkreldis.2005.10.001. Epub 2005 Dec 20. Parkinsonism Relat Disord. 2006. PMID: 16368257 No abstract available.
345 results