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Page 1
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis.
Teyssou E, Muratet F, Amador MD, Ferrien M, Lautrette G, Machat S, Boillée S, Larmonier T, Saker S, Leguern E, Cazeneuve C, Marie Y, Guegan J, Gyorgy B, Cintas P, Meininger V, Le Forestier N, Salachas F, Couratier P, Camu W, Seilhean D, Millecamps S. Teyssou E, et al. Among authors: leguern e. Neurobiol Aging. 2021 Mar;99:102.e11-102.e20. doi: 10.1016/j.neurobiolaging.2020.10.015. Epub 2020 Oct 23. Neurobiol Aging. 2021. PMID: 33218681
Recurrent polyradiculoneuropathy with the 17p11.2 deletion.
Le Forestier N, LeGuern E, Coullin P, Birouk N, Maisonobe T, Brice A, Léger JM, Bouche P. Le Forestier N, et al. Among authors: leguern e. Muscle Nerve. 1997 Sep;20(9):1184-6. doi: 10.1002/(sici)1097-4598(199709)20:9<1184::aid-mus16>3.0.co;2-t. Muscle Nerve. 1997. PMID: 9270678
[Hereditary neuropathy with liability to pressure palsies].
Bouche P, Mouton P, Gouider R, Dubourg O, Le Guern E, Maisonobe T, le Forestier N. Bouche P, et al. Rev Neurol (Paris). 2000 Oct;156(10):915-9. Rev Neurol (Paris). 2000. PMID: 11033525 Review. French. No abstract available.
Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis.
Millecamps S, Da Barroca S, Cazeneuve C, Salachas F, Pradat PF, Danel-Brunaud V, Vandenberghe N, Lacomblez L, Le Forestier N, Bruneteau G, Camu W, Brice A, Meininger V, LeGuern E. Millecamps S, et al. Among authors: leguern e. Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):E107; author reply E108. doi: 10.1073/pnas.1006190107. Epub 2010 Jun 10. Proc Natl Acad Sci U S A. 2010. PMID: 20538972 Free PMC article. No abstract available.
Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient.
Hernandez Lain A, Millecamps S, Dubourg O, Salachas F, Bruneteau G, Lacomblez L, LeGuern E, Seilhean D, Duyckaerts C, Meininger V, Mallet J, Pradat PF. Hernandez Lain A, et al. Among authors: leguern e. J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1414-6. doi: 10.1136/jnnp.2010.208868. Epub 2010 Jun 18. J Neurol Neurosurg Psychiatry. 2011. PMID: 20562395 No abstract available.
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: leguern e. 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.
242 results