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Giant axonal neuropathy.
Handb Clin Neurol. 2013;115:933-8. doi: 10.1016/B978-0-444-52902-2.00052-7.
Handb Clin Neurol. 2013.
PMID: 23931822
Review.
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study.
Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, Haytural H, Foroud T, Myers RH, Sassi SB, Hentati E, Nabli F, Farhat E, Amouri R, Hentati F, Farrer MJ.
Trinh J, et al. Among authors: hentati e.
Lancet Neurol. 2016 Nov;15(12):1248-1256. doi: 10.1016/S1474-4422(16)30203-4. Epub 2016 Sep 28.
Lancet Neurol. 2016.
PMID: 27692902
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Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease.
Ben Sassi S, Nabli F, Hentati E, Nahdi H, Trabelsi M, Ben Ayed H, Amouri R, Duda JE, Farrer MJ, Hentati F.
Ben Sassi S, et al. Among authors: hentati e.
Parkinsonism Relat Disord. 2012 Mar;18(3):243-6. doi: 10.1016/j.parkreldis.2011.10.009. Epub 2011 Nov 6.
Parkinsonism Relat Disord. 2012.
PMID: 22056842
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Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism.
Trinh J, Amouri R, Duda JE, Morley JF, Read M, Donald A, Vilariño-Güell C, Thompson C, Szu Tu C, Gustavsson EK, Ben Sassi S, Hentati E, Zouari M, Farhat E, Nabli F, Hentati F, Farrer MJ.
Trinh J, et al. Among authors: hentati e.
Neurobiol Aging. 2014 May;35(5):1125-31. doi: 10.1016/j.neurobiolaging.2013.11.015. Epub 2013 Nov 22.
Neurobiol Aging. 2014.
PMID: 24355527
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Disability progression in multiple sclerosis: a Tunisian prospective cohort study.
Hentati E, Ben Sassi S, Nabli F, Mabrouk T, Zouari M, Hentati F.
Hentati E, et al.
Neurol Sci. 2018 May;39(5):879-884. doi: 10.1007/s10072-018-3295-4. Epub 2018 Feb 23.
Neurol Sci. 2018.
PMID: 29476286
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Translation initiator EIF4G1 mutations in familial Parkinson disease.
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, Kreisler A, Ross OA, Nishioka K, Soto-Ortolaza AI, Cobb SA, Melrose HL, Behrouz B, Keeling BH, Bacon JA, Hentati E, Williams L, Yanagiya A, Sonenberg N, Lockhart PJ, Zubair AC, Uitti RJ, Aasly JO, Krygowska-Wajs A, Opala G, Wszolek ZK, Frigerio R, Maraganore DM, Gosal D, Lynch T, Hutchinson M, Bentivoglio AR, Valente EM, Nichols WC, Pankratz N, Foroud T, Gibson RA, Hentati F, Dickson DW, Destée A, Farrer MJ.
Chartier-Harlin MC, et al. Among authors: hentati e.
Am J Hum Genet. 2011 Sep 9;89(3):398-406. doi: 10.1016/j.ajhg.2011.08.009.
Am J Hum Genet. 2011.
PMID: 21907011
Free PMC article.
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Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.
Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Hentati E, Hentati F, Farrer MJ.
Nishioka K, et al. Among authors: hentati e.
Parkinsonism Relat Disord. 2010 Dec;16(10):686-7. doi: 10.1016/j.parkreldis.2010.09.007. Epub 2010 Oct 23.
Parkinsonism Relat Disord. 2010.
PMID: 20971673
Free PMC article.
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VPS35 mutations in Parkinson disease.
Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, Conibear E, Wasserman WW, Aasly JO, Burkhard PR, Djaldetti R, Ghika J, Hentati F, Krygowska-Wajs A, Lynch T, Melamed E, Rajput A, Rajput AH, Solida A, Wu RM, Uitti RJ, Wszolek ZK, Vingerhoets F, Farrer MJ.
Vilariño-Güell C, et al. Among authors: hentati e.
Am J Hum Genet. 2011 Jul 15;89(1):162-7. doi: 10.1016/j.ajhg.2011.06.001.
Am J Hum Genet. 2011.
PMID: 21763482
Free PMC article.
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