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Reply to the letter from Gazulla et al.
Corcia P, Lunetta C, Couratier P, Vourc'h P, Gromicho M, Desnuelle C, Soriani MH, Pinto S, de Carvalho M. Corcia P, et al. Eur J Neurol. 2022 Jan;29(1):e3-e4. doi: 10.1111/ene.15134. Epub 2021 Oct 18. Eur J Neurol. 2022. PMID: 34624147 No abstract available.
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.
[Genetics of motor neuron disorders].
Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Rev Neurol (Paris). 2008 Feb;164(2):115-30. doi: 10.1016/j.neurol.2007.10.002. Epub 2008 Feb 20. Rev Neurol (Paris). 2008. PMID: 18358870 Review. French.
Respiratory onset in an ALS family with L144F SOD1 mutation.
Corcia P, Petiot P, Stevic Z, Vourc'h P, Morales R, Gordon PH, Pageot N, Andres C, Camu W. Corcia P, et al. J Neurol Neurosurg Psychiatry. 2011 Jul;82(7):747-9. doi: 10.1136/jnnp.2009.197558. Epub 2010 Jun 20. J Neurol Neurosurg Psychiatry. 2011. PMID: 20562451
175 results