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Page 1
Paraoxonase cluster polymorphisms are associated with sporadic ALS.
Saeed M, Siddique N, Hung WY, Usacheva E, Liu E, Sufit RL, Heller SL, Haines JL, Pericak-Vance M, Siddique T. Saeed M, et al. Among authors: sufit rl. Neurology. 2006 Sep 12;67(5):771-6. doi: 10.1212/01.wnl.0000227187.52002.88. Epub 2006 Jul 5. Neurology. 2006. PMID: 16822964
Lack of association of VEGF promoter polymorphisms with sporadic ALS.
Chen W, Saeed M, Mao H, Siddique N, Dellefave L, Hung WY, Deng HX, Sufit RL, Heller SL, Haines JL, Pericak-Vance M, Siddique T. Chen W, et al. Among authors: sufit rl. Neurology. 2006 Aug 8;67(3):508-10. doi: 10.1212/01.wnl.0000227926.42370.04. Neurology. 2006. PMID: 16894118
Riluzole metabolism and CYP1A1/2 polymorphisms in patients with ALS.
Ajroud-Driss S, Saeed M, Khan H, Siddique N, Hung WY, Sufit R, Heller S, Armstrong J, Casey P, Siddique T, Lukas TJ. Ajroud-Driss S, et al. Among authors: sufit r. Amyotroph Lateral Scler. 2007 Oct;8(5):305-9. doi: 10.1080/17482960701500650. Amyotroph Lateral Scler. 2007. PMID: 17852022 Clinical Trial.
Oculomotor involvement in myotonic dystrophy type 2.
Ajroud-Driss S, Sufit R, Siddique T, Hain TC. Ajroud-Driss S, et al. Among authors: sufit r. Muscle Nerve. 2008 Oct;38(4):1326-9. doi: 10.1002/mus.21113. Muscle Nerve. 2008. PMID: 18785188
Amyotrophic lateral sclerosis and sarcoidosis.
Ajroud-Driss S, Wolfe L, Sufit R. Ajroud-Driss S, et al. Among authors: sufit r. Muscle Nerve. 2009 Nov;40(5):903. doi: 10.1002/mus.21421. Muscle Nerve. 2009. PMID: 19697365 No abstract available.
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, Bigio EH, Brooks BR, Ajroud K, Sufit RL, Haines JL, Mugnaini E, Pericak-Vance MA, Siddique T. Deng HX, et al. Among authors: sufit rl. Nature. 2011 Aug 21;477(7363):211-5. doi: 10.1038/nature10353. Nature. 2011. PMID: 21857683 Free PMC article.
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.
Fecto F, Yan J, Vemula SP, Liu E, Yang Y, Chen W, Zheng JG, Shi Y, Siddique N, Arrat H, Donkervoort S, Ajroud-Driss S, Sufit RL, Heller SL, Deng HX, Siddique T. Fecto F, et al. Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250. Arch Neurol. 2011. PMID: 22084127
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Ahmeti KB, Ajroud-Driss S, Al-Chalabi A, Andersen PM, Armstrong J, Birve A, Blauw HM, Brown RH, Bruijn L, Chen W, Chio A, Comeau MC, Cronin S, Diekstra FP, Soraya Gkazi A, Glass JD, Grab JD, Groen EJ, Haines JL, Hardiman O, Heller S, Huang J, Hung WY; ITALSGEN consortium; Jaworski JM, Jones A, Khan H, Landers JE, Langefeld CD, Leigh PN, Marion MC, McLaughlin RL, Meininger V, Melki J, Miller JW, Mora G, Pericak-Vance MA, Rampersaud E, Robberecht W, Russell LP, Salachas F, Saris CG, Shatunov A, Shaw CE, Siddique N, Siddique T, Smith BN, Sufit R, Topp S, Traynor BJ, Vance C, van Damme P, van den Berg LH, van Es MA, van Vught PW, Veldink JH, Yang Y, Zheng JG; ALSGEN Consortium. Ahmeti KB, et al. Among authors: sufit r. Neurobiol Aging. 2013 Jan;34(1):357.e7-19. doi: 10.1016/j.neurobiolaging.2012.07.017. Epub 2012 Sep 5. Neurobiol Aging. 2013. PMID: 22959728 Free PMC article.
110 results