Ajroud-Driss S - Search Results

1

A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs.

Ajroud-Driss S, Fecto F, Ajroud K, Yang Y, Donkervoort S, Siddique N, Siddique T. Ajroud-Driss S, et al. Neurogenetics. 2009 Oct;10(4):359-61. doi: 10.1007/s10048-009-0188-y. Epub 2009 Apr 7. Neurogenetics. 2009. PMID: 19350291 No abstract available.

2

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.

Ajroud-Driss S, Fecto F, Ajroud K, Lalani I, Calvo SE, Mootha VK, Deng HX, Siddique N, Tahmoush AJ, Heiman-Patterson TD, Siddique T. Ajroud-Driss S, et al. Neurogenetics. 2015 Jan;16(1):1-9. doi: 10.1007/s10048-014-0421-1. Epub 2014 Sep 6. Neurogenetics. 2015. PMID: 25193783 Free PMC article.

3

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. 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.

4

Familial amyotrophic lateral sclerosis, a historical perspective.

Siddique T, Ajroud-Driss S. Siddique T, et al. Acta Myol. 2011 Oct;30(2):117-20. Acta Myol. 2011. PMID: 22106714 Free PMC article. Review.

5

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. Ann Neurol. 2010 Jun;67(6):739-48. doi: 10.1002/ana.22051. Ann Neurol. 2010. PMID: 20517935 Free PMC article.

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. Arch Neurol. 2011 Aug;68(8):1057-61. doi: 10.1001/archneurol.2011.178. Arch Neurol. 2011. PMID: 21825243 Free PMC article.

7

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

8

Sporadic and hereditary amyotrophic lateral sclerosis (ALS).

Ajroud-Driss S, Siddique T. Ajroud-Driss S, et al. Biochim Biophys Acta. 2015 Apr;1852(4):679-84. doi: 10.1016/j.bbadis.2014.08.010. Epub 2014 Sep 1. Biochim Biophys Acta. 2015. PMID: 25193032 Free article. Review.

9

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. Amyotroph Lateral Scler. 2007 Oct;8(5):305-9. doi: 10.1080/17482960701500650. Amyotroph Lateral Scler. 2007. PMID: 17852022 Clinical Trial.

10

Oculomotor involvement in myotonic dystrophy type 2.

Ajroud-Driss S, Sufit R, Siddique T, Hain TC. Ajroud-Driss S, et al. Muscle Nerve. 2008 Oct;38(4):1326-9. doi: 10.1002/mus.21113. Muscle Nerve. 2008. PMID: 18785188

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