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308 results
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Progression in ALS is not linear but is curvilinear.
Gordon PH, Cheng B, Salachas F, Pradat PF, Bruneteau G, Corcia P, Lacomblez L, Meininger V. Gordon PH, et al. Among authors: meininger v. J Neurol. 2010 Oct;257(10):1713-7. doi: 10.1007/s00415-010-5609-1. Epub 2010 Jun 8. J Neurol. 2010. PMID: 20532545
[What's new in primary lateral sclerosis?].
Le Forestier N, Maisonobe T, Spelle L, Lesort A, Salachas F, Chassande B, Bouche P, Samson Y, Meininger V. Le Forestier N, et al. Among authors: meininger v. Rev Neurol (Paris). 2000 Apr;156(4):364-71. Rev Neurol (Paris). 2000. PMID: 10795013 French.
[TBK1 gene stresses the major role of autophagy in ALS].
Corcia P, Beltran S, Vourc'h P, Meininger V, Couratier P. Corcia P, et al. Among authors: meininger v. Rev Neurol (Paris). 2015 Nov;171(11):747-9. doi: 10.1016/j.neurol.2015.10.004. Rev Neurol (Paris). 2015. PMID: 26573965 French. No abstract available.
[Multifocal motor neuropathies with conduction blocks. 39 cases].
Le Forestier N, Chassande B, Moulonguet A, Maisonobe T, Schaeffer S, Birouk N, Baumann N, Adams D, Léger JM, Meininger V, Said G, Bouche P. Le Forestier N, et al. Among authors: meininger v. Rev Neurol (Paris). 1997 Oct;153(10):579-86. Rev Neurol (Paris). 1997. PMID: 9684022 French.
[Tolerance of riluzole in a phase IIIb clinical trial].
Lacomblez L, Dib M, Doppler V, Faudet A, Robin V, Salachas F, Bensimon G, Meininger V. Lacomblez L, et al. Among authors: meininger v. Therapie. 2002 Jan-Feb;57(1):65-71. Therapie. 2002. PMID: 12090150 Clinical Trial. French.
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.
Millecamps S, Corcia P, Cazeneuve C, Boillée S, Seilhean D, Danel-Brunaud V, Vandenberghe N, Pradat PF, Le Forestier N, Lacomblez L, Bruneteau G, Camu W, Brice A, Meininger V, LeGuern E, Salachas F. Millecamps S, et al. Among authors: meininger v. Neurobiol Aging. 2012 Apr;33(4):839.e1-3. doi: 10.1016/j.neurobiolaging.2011.11.010. Epub 2011 Dec 9. Neurobiol Aging. 2012. PMID: 22169395
Phenotypic and genotypic studies of ALS cases in ALS-SMA families.
Corcia P, Vourc'h P, Blasco H, Couratier P, Dangoumau A, Bellance R, Desnuelle C, Viader F, Pautot V, Millecamps S, Bakkouche S, Salachas F, Andres CR, Meininger V, Camu W. Corcia P, et al. Among authors: meininger v. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):432-437. doi: 10.1080/21678421.2018.1440406. Epub 2018 Mar 1. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29493298
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S, Boillée S, Le Ber I, Seilhean D, Teyssou E, Giraudeau M, Moigneu C, Vandenberghe N, Danel-Brunaud V, Corcia P, Pradat PF, Le Forestier N, Lacomblez L, Bruneteau G, Camu W, Brice A, Cazeneuve C, Leguern E, Meininger V, Salachas F. Millecamps S, et al. Among authors: meininger v. J Med Genet. 2012 Apr;49(4):258-63. doi: 10.1136/jmedgenet-2011-100699. J Med Genet. 2012. PMID: 22499346
308 results