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Page 1
Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
Megat S, Mora N, Sanogo J, Roman O, Catanese A, Alami NO, Freischmidt A, Mingaj X, De Calbiac H, Muratet F, Dirrig-Grosch S, Dieterle S, Van Bakel N, Müller K, Sieverding K, Weishaupt J, Andersen PM, Weber M, Neuwirth C, Margelisch M, Sommacal A, Van Eijk KR, Veldink JH; Project Mine Als Sequencing Consortium; Lautrette G, Couratier P, Camuzat A, Le Ber I, Grassano M, Chio A, Boeckers T, Ludolph AC, Roselli F, Yilmazer-Hanke D, Millecamps S, Kabashi E, Storkebaum E, Sellier C, Dupuis L. Megat S, et al. Among authors: lautrette g. Nat Commun. 2023 Jan 20;14(1):342. doi: 10.1038/s41467-022-35724-1. Nat Commun. 2023. PMID: 36670122 Free PMC article.
Early onset Parkinsonism associated with an intronic SOD1 mutation.
Kacem I, Funalot B, Torny F, Lautrette G, Andersen PM, Couratier P. Kacem I, et al. Among authors: lautrette g. Amyotroph Lateral Scler. 2012 May;13(3):315-7. doi: 10.3109/17482968.2011.623301. Epub 2012 Jan 3. Amyotroph Lateral Scler. 2012. PMID: 22214312
Population-based epidemiology of amyotrophic lateral sclerosis (ALS) in an ageing Europe--the French register of ALS in Limousin (FRALim register).
Marin B, Hamidou B, Couratier P, Nicol M, Delzor A, Raymondeau M, Druet-Cabanac M, Lautrette G, Boumediene F, Preux PM; French register of ALS in Limousin. Marin B, et al. Among authors: lautrette g. Eur J Neurol. 2014 Oct;21(10):1292-300, e78-9. doi: 10.1111/ene.12474. Epub 2014 Jun 9. Eur J Neurol. 2014. PMID: 24909935
Epidemiology of amyotrophic lateral sclerosis: A review of literature.
Couratier P, Corcia P, Lautrette G, Nicol M, Preux PM, Marin B. Couratier P, et al. Among authors: lautrette g. Rev Neurol (Paris). 2016 Jan;172(1):37-45. doi: 10.1016/j.neurol.2015.11.002. Epub 2015 Dec 22. Rev Neurol (Paris). 2016. PMID: 26727307 Review.
Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centres.
Marin B, Beghi E, Vial C, Bernard E, Lautrette G, Clavelou P, Guy N, Lemasson G, Debruxelles S, Cintas P, Antoine JC, Camdessanche JP, Logroscino G, Preux PM, Couratier P; EURECALS consortium. Marin B, et al. Among authors: lautrette g. Eur J Neurol. 2016 Apr;23(4):787-95. doi: 10.1111/ene.12941. Epub 2016 Feb 1. Eur J Neurol. 2016. PMID: 26833536
ALS and frontotemporal dementia belong to a common disease spectrum.
Couratier P, Corcia P, Lautrette G, Nicol M, Marin B. Couratier P, et al. Among authors: lautrette g. Rev Neurol (Paris). 2017 May;173(5):273-279. doi: 10.1016/j.neurol.2017.04.001. Epub 2017 Apr 24. Rev Neurol (Paris). 2017. PMID: 28449882 Review.
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis.
Teyssou E, Chartier L, Amador MD, Lam R, Lautrette G, Nicol M, Machat S, Da Barroca S, Moigneu C, Mairey M, Larmonier T, Saker S, Dussert C, Forlani S, Fontaine B, Seilhean D, Bohl D, Boillée S, Meininger V, Couratier P, Salachas F, Stevanin G, Millecamps S. Teyssou E, et al. Among authors: lautrette g. Neurobiol Aging. 2017 Oct;58:239.e11-239.e20. doi: 10.1016/j.neurobiolaging.2017.06.018. Epub 2017 Jun 24. Neurobiol Aging. 2017. PMID: 28716533 Free article.
Exploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment.
Hamidou B, Marin B, Lautrette G, Nicol M, Camu W, Corcia P, Arnes-Bes MC, Tranchant C, Clavelou P, Hannequin D, Maurice G, Beauvais K, Antoine JC, Danel-Brunaud V, Viader F, Preux PM, Couratier P. Hamidou B, et al. Among authors: lautrette g. Amyotroph Lateral Scler Frontotemporal Degener. 2017 Nov;18(7-8):519-527. doi: 10.1080/21678421.2017.1353098. Epub 2017 Aug 1. Amyotroph Lateral Scler Frontotemporal Degener. 2017. PMID: 28762856
55 results