Siddique T - Search Results

1

Cholinergic denervation in a pure multi-infarct state: observations on CADASIL.

Mesulam M, Siddique T, Cohen B. Mesulam M, et al. Among authors: siddique t. Neurology. 2003 Apr 8;60(7):1183-5. doi: 10.1212/01.wnl.0000055927.22611.eb. Neurology. 2003. PMID: 12682331

2

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

3

Genetic aspects of amyotrophic lateral sclerosis.

Siddique T, Lalani I. Siddique T, et al. Adv Neurol. 2002;88:21-32. Adv Neurol. 2002. PMID: 11908227 Review. No abstract available.

4

Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.

Li X, Rowland LP, Mitsumoto H, Przedborski S, Bird TD, Schellenberg GD, Peskind E, Johnson N, Siddique T, Mesulam MM, Weintraub S, Mastrianni JA. Li X, et al. Among authors: siddique t. Ann Neurol. 2005 Dec;58(6):858-64. doi: 10.1002/ana.20646. Ann Neurol. 2005. PMID: 16315279

5

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

Vance C, Al-Chalabi A, Ruddy D, Smith BN, Hu X, Sreedharan J, Siddique T, Schelhaas HJ, Kusters B, Troost D, Baas F, de Jong V, Shaw CE. Vance C, et al. Among authors: siddique t. Brain. 2006 Apr;129(Pt 4):868-76. doi: 10.1093/brain/awl030. Epub 2006 Feb 22. Brain. 2006. PMID: 16495328 Free article.

6

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.

Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Among authors: siddique n, siddique t. Ann Neurol. 2010 Jun;67(6):739-48. doi: 10.1002/ana.22051. Ann Neurol. 2010. PMID: 20517935 Free PMC article.

7

Recent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2.

Ajroud-Driss S, Deng HX, Siddique T. Ajroud-Driss S, et al. Among authors: siddique t. Curr Neurol Neurosci Rep. 2011 Jun;11(3):262-73. doi: 10.1007/s11910-011-0185-z. Curr Neurol Neurosci Rep. 2011. PMID: 21327736 Review.

8

Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.

Deng HX, Bigio EH, Zhai H, Fecto F, Ajroud K, Shi Y, Yan J, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Among authors: siddique n, siddique t. Arch Neurol. 2011 Aug;68(8):1057-61. doi: 10.1001/archneurol.2011.178. Arch Neurol. 2011. PMID: 21825243 Free PMC article.

9

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. Among authors: siddique n, siddique t. Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250. Arch Neurol. 2011. PMID: 22084127

10

What is repeated in ALS and FTLD.

Fecto F, Siddique T. Fecto F, et al. Among authors: siddique t. Lancet Neurol. 2012 Jan;11(1):25-7. doi: 10.1016/S1474-4422(11)70275-7. Epub 2011 Dec 7. Lancet Neurol. 2012. PMID: 22154784 No abstract available.

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