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Items: 23


NaV channel variants in patients with painful and nonpainful peripheral neuropathy.

Wadhawan S, Pant S, Golhar R, Kirov S, Thompson J, Jacobsen L, Qureshi I, Ajroud-Driss S, Freeman R, Simpson DM, Smith AG, Hoke A, Bristow LJ.

Neurol Genet. 2017 Dec 15;3(6):e207. doi: 10.1212/NXG.0000000000000207. eCollection 2017 Dec.


Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutations.

Lange DJ, Shahbazi M, Silani V, Ludolph AC, Weishaupt JH, Ajroud-Driss S, Fields KG, Remanan R, Appel SH, Morelli C, Doretti A, Maderna L, Messina S, Weiland U, Marklund SL, Andersen PM.

Ann Neurol. 2017 Jun;81(6):837-848. doi: 10.1002/ana.24950. Epub 2017 Jun 9.


Respiratory Pattern and Tidal Volumes Differ for Pressure Support and Volume-assured Pressure Support in Amyotrophic Lateral Sclerosis.

Nicholson TT, Smith SB, Siddique T, Sufit R, Ajroud-Driss S, Coleman JM 3rd, Wolfe LF.

Ann Am Thorac Soc. 2017 Jul;14(7):1139-1146. doi: 10.1513/AnnalsATS.201605-346OC.


Open label study to assess the safety of VM202 in subjects with amyotrophic lateral sclerosis.

Sufit RL, Ajroud-Driss S, Casey P, Kessler JA.

Amyotroph Lateral Scler Frontotemporal Degener. 2017 May;18(3-4):269-278. doi: 10.1080/21678421.2016.1259334. Epub 2017 Feb 6.


Double-blind, placebo-controlled study of HGF gene therapy in diabetic neuropathy.

Kessler JA, Smith AG, Cha BS, Choi SH, Wymer J, Shaibani A, Ajroud-Driss S, Vinik A; VM202 DPN-II Study Group.

Ann Clin Transl Neurol. 2015 May;2(5):465-78. doi: 10.1002/acn3.186. Epub 2015 Mar 5.


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.

Neurogenetics. 2015 Jan;16(1):1-9. doi: 10.1007/s10048-014-0421-1. Epub 2014 Sep 6.


Sporadic and hereditary amyotrophic lateral sclerosis (ALS).

Ajroud-Driss S, Siddique T.

Biochim Biophys Acta. 2015 Apr;1852(4):679-84. doi: 10.1016/j.bbadis.2014.08.010. Epub 2014 Sep 1. Review.


Molecular mechanisms and animal models of spinal muscular atrophy.

Edens BM, Ajroud-Driss S, Ma L, Ma YC.

Biochim Biophys Acta. 2015 Apr;1852(4):685-92. doi: 10.1016/j.bbadis.2014.07.024. Epub 2014 Aug 1. Review.


Phase 1/2 open-label dose-escalation study of plasmid DNA expressing two isoforms of hepatocyte growth factor in patients with painful diabetic peripheral neuropathy.

Ajroud-Driss S, Christiansen M, Allen JA, Kessler JA.

Mol Ther. 2013 Jun;21(6):1279-86. doi: 10.1038/mt.2013.69. Epub 2013 Apr 23.


Gastrostomy tube placement by endoscopy versus radiologic methods in patients with ALS: a retrospective study of complications and outcome.

Allen JA, Chen R, Ajroud-Driss S, Sufit RL, Heller S, Siddique T, Wolfe L.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14(4):308-14. doi: 10.3109/21678421.2012.751613. Epub 2013 Jan 4.


Prevalence and characteristics of pain in early and late stages of ALS.

Rivera I, Ajroud-Driss S, Casey P, Heller S, Allen J, Siddique T, Sufit R.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 Sep;14(5-6):369-72. doi: 10.3109/21678421.2012.751614. Epub 2013 Jan 4.


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.

Neurobiol Aging. 2013 Jan;34(1):357.e7-19. doi: 10.1016/j.neurobiolaging.2012.07.017. Epub 2012 Sep 5.


Familial amyotrophic lateral sclerosis, a historical perspective.

Siddique T, Ajroud-Driss S.

Acta Myol. 2011 Oct;30(2):117-20. Review.


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.

Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250.


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.

Arch Neurol. 2011 Aug;68(8):1057-61. doi: 10.1001/archneurol.2011.178.


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

Ajroud-Driss S, Deng HX, Siddique T.

Curr Neurol Neurosci Rep. 2011 Jun;11(3):262-73. doi: 10.1007/s11910-011-0185-z. Review.


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.

Ann Neurol. 2010 Jun;67(6):739-48. doi: 10.1002/ana.22051.


Small fiber neuropathy following vaccination for rabies, varicella or Lyme disease.

Souayah N, Ajroud-Driss S, Sander HW, Brannagan TH, Hays AP, Chin RL.

Vaccine. 2009 Dec 9;27(52):7322-5. doi: 10.1016/j.vaccine.2009.09.077. Epub 2009 Oct 4.


Amyotrophic lateral sclerosis and sarcoidosis.

Ajroud-Driss S, Wolfe L, Sufit R.

Muscle Nerve. 2009 Nov;40(5):903. doi: 10.1002/mus.21421. No abstract available.


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.

Neurogenetics. 2009 Oct;10(4):359-61. doi: 10.1007/s10048-009-0188-y. Epub 2009 Apr 7. No abstract available.


Oculomotor involvement in myotonic dystrophy type 2.

Ajroud-Driss S, Sufit R, Siddique T, Hain TC.

Muscle Nerve. 2008 Oct;38(4):1326-9. doi: 10.1002/mus.21113.


Gender difference in levels of Cu/Zn superoxide dismutase (SOD1) in cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

Frutiger K, Lukas TJ, Gorrie G, Ajroud-Driss S, Siddique T.

Amyotroph Lateral Scler. 2008 Jun;9(3):184-7. doi: 10.1080/17482960801984358.


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.

Amyotroph Lateral Scler. 2007 Oct;8(5):305-9.


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