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Page 1
The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler. 2011 May;12(3):210-4. doi: 10.3109/17482968.2010.522587. Epub 2010 Oct 11.
Amyotroph Lateral Scler. 2011.
PMID: 20932227
Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis.
Praline J, Blasco H, Vourc'h P, Rat V, Gendrot C, Camu W, Andres CR; French ALS Study Group.
Praline J, et al.
J Neurol Sci. 2012 Jun 15;317(1-2):58-61. doi: 10.1016/j.jns.2012.02.029. Epub 2012 Mar 14.
J Neurol Sci. 2012.
PMID: 22425014
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A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS.
Blasco H, Bernard-Marissal N, Vourc'h P, Guettard YO, Sunyach C, Augereau O, Khederchah J, Mouzat K, Antar C, Gordon PH, Veyrat-Durebex C, Besson G, Andersen PM, Salachas F, Meininger V, Camu W, Pettmann B, Andres CR, Corcia P; French ALS Study Group.
Blasco H, et al.
Hum Mutat. 2013 Jul;34(7):953-60. doi: 10.1002/humu.22329. Epub 2013 May 28.
Hum Mutat. 2013.
PMID: 23568759
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Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS.
Martin I, Vourc'h P, Mahé M, Thépault RA, Antar C, Védrine S, Praline J, Camu W, Andres CR, Corcia P; French ALS Study Group.
Martin I, et al.
Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):432-5. doi: 10.3109/17482960802444972.
Amyotroph Lateral Scler. 2009.
PMID: 19922136
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Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis.
Blasco H, Vourc'h P, Nadjar Y, Ribourtout B, Gordon PH, Guettard YO, Camu W, Praline J, Meininger V, Andres CR, Corcia P; French ALS study group.
Blasco H, et al.
J Neurol Sci. 2011 Apr 15;303(1-2):124-7. doi: 10.1016/j.jns.2010.12.018. Epub 2011 Jan 26.
J Neurol Sci. 2011.
PMID: 21276595
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APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in men.
Praline J, Blasco H, Vourc'h P, Garrigue MA, Gordon PH, Camu W, Corcia P, Andres CR; French ALS Study Group.
Praline J, et al.
Eur J Neurol. 2011 Aug;18(8):1046-52. doi: 10.1111/j.1468-1331.2010.03330.x. Epub 2011 Jan 20.
Eur J Neurol. 2011.
PMID: 21251163
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SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.
Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group.
Corcia P, et al.
Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23.
Neurology. 2006.
PMID: 16931506
Clinical Trial.
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