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Impact of a frequent nearsplice SOD1 variant in amyotrophic lateral sclerosis: optimising SOD1 genetic screening for gene therapy opportunities.
Muratet F, Teyssou E, Chiot A, Boillée S, Lobsiger CS, Bohl D, Gyorgy B, Guegan J, Marie Y, Amador MDM, Salachas F, Meininger V, Bernard E, Antoine JC, Camdessanché JP, Camu W, Cazeneuve C, Fauret-Amsellem AL, Leguern E, Mouzat K, Guissart C, Lumbroso S, Corcia P, Vourc'h P, Grapperon AM, Attarian S, Verschueren A, Seilhean D, Millecamps S. Muratet F, et al. Among authors: seilhean d. J Neurol Neurosurg Psychiatry. 2021 Sep;92(9):942-949. doi: 10.1136/jnnp-2020-325921. Epub 2021 Mar 30. J Neurol Neurosurg Psychiatry. 2021. PMID: 33785574
Dementia in two histologically confirmed cases of multiple sclerosis: one case with isolated dementia and one case associated with psychiatric symptoms.
Fontaine B, Seilhean D, Tourbah A, Daumas-Duport C, Duyckaerts C, Benoit N, Devaux B, Hauw JJ, Rancurel G, Lyon-Caen O. Fontaine B, et al. Among authors: seilhean d. J Neurol Neurosurg Psychiatry. 1994 Mar;57(3):353-9. doi: 10.1136/jnnp.57.3.353. J Neurol Neurosurg Psychiatry. 1994. PMID: 8158186 Free PMC article.
Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions.
Seilhean D, Takahashi J, El Hachimi KH, Fujigasaki H, Lebre AS, Biancalana V, Dürr A, Salachas F, Hogenhuis J, de Thé H, Hauw JJ, Meininger V, Brice A, Duyckaerts C. Seilhean D, et al. Acta Neuropathol. 2004 Jul;108(1):81-7. doi: 10.1007/s00401-004-0855-x. Epub 2004 Apr 27. Acta Neuropathol. 2004. PMID: 15114487
Causes of death in a post-mortem series of ALS patients.
Corcia P, Pradat PF, Salachas F, Bruneteau G, Forestier Nl, Seilhean D, Hauw JJ, Meininger V. Corcia P, et al. Among authors: seilhean d. Amyotroph Lateral Scler. 2008;9(1):59-62. doi: 10.1080/17482960701656940. Amyotroph Lateral Scler. 2008. PMID: 17924236
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis.
Dupuis L, Corcia P, Fergani A, Gonzalez De Aguilar JL, Bonnefont-Rousselot D, Bittar R, Seilhean D, Hauw JJ, Lacomblez L, Loeffler JP, Meininger V. Dupuis L, et al. Among authors: seilhean d. Neurology. 2008 Mar 25;70(13):1004-9. doi: 10.1212/01.wnl.0000285080.70324.27. Epub 2008 Jan 16. Neurology. 2008. PMID: 18199832
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A; French Research Network on FTD/FTD-MND. Le Ber I, et al. Among authors: seilhean d. Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c. Neurology. 2009. PMID: 19433740
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: seilhean d. 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.
204 results