Siddique T - Search Results

1

Genome-wide analysis of the parkinsonism-dementia complex of Guam.

Morris HR, Steele JC, Crook R, Wavrant-De Vrièze F, Onstead-Cardinale L, Gwinn-Hardy K, Wood NW, Farrer M, Lees AJ, McGeer PL, Siddique T, Hardy J, Perez-Tur J. Morris HR, et al. Among authors: siddique t. Arch Neurol. 2004 Dec;61(12):1889-97. doi: 10.1001/archneur.61.12.1889. Arch Neurol. 2004. PMID: 15596609

2

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.

3

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.

El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. El Euch-Fayache G, et al. Among authors: siddique t. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855

4

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

5

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

6

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.

7

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

8

A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosis.

Aksoy H, Dean G, Elian M, Deng HX, Deng G, Juneja T, Storey E, McKinlay Gardner RJ, Jacob RL, Laing NG, Siddique T. Aksoy H, et al. Among authors: siddique t. Neuroepidemiology. 2003 Jul-Aug;22(4):235-8. doi: 10.1159/000070564. Neuroepidemiology. 2003. PMID: 12792143

9

Presence of dendritic cells, MCP-1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue.

Henkel JS, Engelhardt JI, Siklós L, Simpson EP, Kim SH, Pan T, Goodman JC, Siddique T, Beers DR, Appel SH. Henkel JS, et al. Among authors: siddique t. Ann Neurol. 2004 Feb;55(2):221-35. doi: 10.1002/ana.10805. Ann Neurol. 2004. PMID: 14755726

10

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.

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