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Page 1
Identification of TMEM230 mutations in familial Parkinson's disease.
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T. Deng HX, et al. Among authors: siddique n, siddique t. Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6. Nat Genet. 2016. PMID: 27270108 Free PMC article.
A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy.
Rezania K, Yan J, Dellefave L, Deng HX, Siddique N, Pascuzzi RT, Siddique T, Roos RP. Rezania K, et al. Among authors: siddique n, siddique t. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):162-6. doi: 10.1080/aml.4.3.162.166. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129803
Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.
Bigio EH, Johnson NA, Rademaker AW, Fung BB, Mesulam MM, Siddique N, Dellefave L, Caliendo J, Freeman S, Siddique T. Bigio EH, et al. Among authors: siddique n, siddique t. J Neuropathol Exp Neurol. 2004 Aug;63(8):801-11. doi: 10.1093/jnen/63.8.801. J Neuropathol Exp Neurol. 2004. PMID: 15330335
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.
Li YJ, Pericak-Vance MA, Haines JL, Siddique N, McKenna-Yasek D, Hung WY, Sapp P, Allen CI, Chen W, Hosler B, Saunders AM, Dellefave LM, Brown RH, Siddique T. Li YJ, et al. Among authors: siddique n, siddique t. Neurogenetics. 2004 Dec;5(4):209-13. doi: 10.1007/s10048-004-0193-0. Epub 2004 Oct 2. Neurogenetics. 2004. PMID: 15657798
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria.
Deng HX, Shi Y, Furukawa Y, Zhai H, Fu R, Liu E, Gorrie GH, Khan MS, Hung WY, Bigio EH, Lukas T, Dal Canto MC, O'Halloran TV, Siddique T. Deng HX, et al. Among authors: siddique t. Proc Natl Acad Sci U S A. 2006 May 2;103(18):7142-7. doi: 10.1073/pnas.0602046103. Epub 2006 Apr 24. Proc Natl Acad Sci U S A. 2006. PMID: 16636275 Free PMC article.
Distal axonopathy in an alsin-deficient mouse model.
Deng HX, Zhai H, Fu R, Shi Y, Gorrie GH, Yang Y, Liu E, Dal Canto MC, Mugnaini E, Siddique T. Deng HX, et al. Among authors: siddique t. Hum Mol Genet. 2007 Dec 1;16(23):2911-20. doi: 10.1093/hmg/ddm251. Epub 2007 Sep 12. Hum Mol Genet. 2007. PMID: 17855450
Genetics of amyotrophic lateral sclerosis.
Siddique N, Siddique T. Siddique N, et al. Among authors: siddique t. Phys Med Rehabil Clin N Am. 2008 Aug;19(3):429-39, vii. doi: 10.1016/j.pmr.2008.05.001. Phys Med Rehabil Clin N Am. 2008. PMID: 18625408 Free PMC article. Review.
261 results