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In ALS, a mutation could be worth two steps.
Corcia P, Blasco H, Beltran S, Andres C, Vourc'h P, Couratier P. Corcia P, et al. Among authors: andres c. Rev Neurol (Paris). 2018 Dec;174(10):669-670. doi: 10.1016/j.neurol.2018.11.001. Rev Neurol (Paris). 2018. PMID: 30501924 No abstract available.
Genetics of amyotrophic lateral sclerosis.
Corcia P, Couratier P, Blasco H, Andres CR, Beltran S, Meininger V, Vourc'h P. Corcia P, et al. Among authors: andres cr. Rev Neurol (Paris). 2017 May;173(5):254-262. doi: 10.1016/j.neurol.2017.03.030. Epub 2017 Apr 25. Rev Neurol (Paris). 2017. PMID: 28449881 Review.
Typical bulbar ALS can be linked to GARS mutation.
Corcia P, Brulard C, Beltran S, Marouillat S, Bakkouche SE, Andres CR, Blasco H, Vourc'h P. Corcia P, et al. Among authors: andres cr. Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):275-277. doi: 10.1080/21678421.2018.1556699. Epub 2019 Jan 20. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30661401
[Genetics of motor neuron disorders].
Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Among authors: andres c. 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.
C-reactive protein: A promising biomarker in ALS?
Corcia P, Blasco H, Beltran S, Andres C, Vourc'h P, Couratier P. Corcia P, et al. Among authors: andres c. Rev Neurol (Paris). 2018 Mar;174(3):104-105. doi: 10.1016/j.neurol.2017.07.001. Epub 2017 Aug 7. Rev Neurol (Paris). 2018. PMID: 28797688 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. Among authors: andres cr. 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.
659 results