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Huntington's disease-like 2 in Brazil--report of 4 patients.
Mov Disord. 2008 Nov 15;23(15):2244-7. doi: 10.1002/mds.22223.
Mov Disord. 2008.
PMID: 18816802
Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.
Rodrigues GR, Walker RH, Bader B, Danek A, Brice A, Cazeneuve C, Russaouen O, Lopes-Cendes I, Marques W Jr, Tumas V.
Rodrigues GR, et al. Among authors: russaouen o.
Arq Neuropsiquiatr. 2011 Jun;69(3):419-23. doi: 10.1590/s0004-282x2011000400002.
Arq Neuropsiquiatr. 2011.
PMID: 21755114
Free article.
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Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation.
Seilhean D, Cazeneuve C, Thuriès V, Russaouen O, Millecamps S, Salachas F, Meininger V, Leguern E, Duyckaerts C.
Seilhean D, et al. Among authors: russaouen o.
Acta Neuropathol. 2009 Oct;118(4):561-73. doi: 10.1007/s00401-009-0545-9. Epub 2009 May 16.
Acta Neuropathol. 2009.
PMID: 19449021
Free article.
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SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V.
Millecamps S, et al. Among authors: russaouen o.
J Med Genet. 2010 Aug;47(8):554-60. doi: 10.1136/jmg.2010.077180. Epub 2010 Jun 24.
J Med Genet. 2010.
PMID: 20577002
Free article.
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