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Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep.
Coutelier M, Andries S, Ghariani S, Dan B, Duyckaerts C, van Rijckevorsel K, Raftopoulos C, Deconinck N, Sonderegger P, Scaravilli F, Vikkula M, Godfraind C. Coutelier M, et al. Among authors: duyckaerts c. Neurology. 2008 Jul 1;71(1):64-6. doi: 10.1212/01.wnl.0000316306.08751.28. Neurology. 2008. PMID: 18591508 No abstract available.
The lipid phosphatase Synaptojanin 1 undergoes a significant alteration in expression and solubility and is associated with brain lesions in Alzheimer's disease.
Ando K, Ndjim M, Turbant S, Fontaine G, Pregoni G, Dauphinot L, Yilmaz Z, Suain V, Mansour S, Authelet M, De Dekker R, Leroy K, Delatour B; Brain Bank NeuroCEB Neuropathology Network; Duyckaerts C, Potier MC, Brion JP. Ando K, et al. Among authors: duyckaerts c. Acta Neuropathol Commun. 2020 Jun 3;8(1):79. doi: 10.1186/s40478-020-00954-1. Acta Neuropathol Commun. 2020. PMID: 32493451 Free PMC article.
Valosin-containing protein gene mutations: clinical and neuropathologic features.
Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D. Guyant-Maréchal L, et al. Among authors: duyckaerts c. Neurology. 2006 Aug 22;67(4):644-51. doi: 10.1212/01.wnl.0000225184.14578.d3. Epub 2006 Jun 21. Neurology. 2006. PMID: 16790606
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: duyckaerts c. Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c. Neurology. 2009. PMID: 19433740
Friedreich's ataxia: oxidative stress and cytoskeletal abnormalities.
Sparaco M, Gaeta LM, Santorelli FM, Passarelli C, Tozzi G, Bertini E, Simonati A, Scaravilli F, Taroni F, Duyckaerts C, Feleppa M, Piemonte F. Sparaco M, et al. Among authors: duyckaerts c. J Neurol Sci. 2009 Dec 15;287(1-2):111-8. doi: 10.1016/j.jns.2009.08.052. Epub 2009 Sep 12. J Neurol Sci. 2009. PMID: 19748629
Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.
Dickson DW, Bergeron C, Chin SS, Duyckaerts C, Horoupian D, Ikeda K, Jellinger K, Lantos PL, Lippa CF, Mirra SS, Tabaton M, Vonsattel JP, Wakabayashi K, Litvan I; Office of Rare Diseases of the National Institutes of Health. Dickson DW, et al. Among authors: duyckaerts c. J Neuropathol Exp Neurol. 2002 Nov;61(11):935-46. doi: 10.1093/jnen/61.11.935. J Neuropathol Exp Neurol. 2002. PMID: 12430710
473 results