Senda Ajroud-Driss - Publications

Neurology Northwestern University, Evanston, IL 

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Burt RK, Balabanov R, Tavee J, Han X, Sufit R, Ajroud-Driss S, Jovanovic B, Quigley K, Arnautovic I, Helenowski I, Sharrack B. Hematopoietic stem cell transplantation for chronic inflammatory demyelinating polyradiculoneuropathy. Journal of Neurology. PMID 32594300 DOI: 10.1007/s00415-020-10010-6  0.32
2017 Nicholson TT, Smith SB, Siddique T, Sufit R, Ajroud-Driss S, Coleman JM, Wolfe LF. Respiratory Pattern and Tidal Volumes Differ for Pressure Support and Volume-Assured Pressure Support in Amyotrophic Lateral Sclerosis. Annals of the American Thoracic Society. PMID 28410001 DOI: 10.1513/Annalsats.201605-346Oc  0.96
2015 Ajroud-Driss S, Fecto F, Ajroud K, Lalani I, Calvo SE, Mootha VK, Deng HX, Siddique N, Tahmoush AJ, Heiman-Patterson TD, Siddique T. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. Neurogenetics. 16: 1-9. PMID 25193783 DOI: 10.1007/S10048-014-0421-1  0.96
2015 Ajroud-Driss S, Siddique T. Sporadic and hereditary amyotrophic lateral sclerosis (ALS). Biochimica Et Biophysica Acta. 1852: 679-684. PMID 25193032 DOI: 10.1016/J.Bbadis.2014.08.010  0.96
2015 Edens BM, Ajroud-Driss S, Ma L, Ma YC. Molecular mechanisms and animal models of spinal muscular atrophy. Biochimica Et Biophysica Acta. 1852: 685-692. PMID 25088406 DOI: 10.1016/J.Bbadis.2014.07.024  0.96
2014 Siddique T, Deng HX, Ajroud-Driss S. Motor Neuron Disease Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.05604-X  0.96
2013 Ajroud-Driss S, Christiansen M, Allen JA, Kessler JA. 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. Molecular Therapy : the Journal of the American Society of Gene Therapy. 21: 1279-86. PMID 23609019 DOI: 10.1038/Mt.2013.69  0.96
2013 Allen JA, Chen R, Ajroud-Driss S, Sufit RL, Heller S, Siddique T, Wolfe L. Gastrostomy tube placement by endoscopy versus radiologic methods in patients with ALS: a retrospective study of complications and outcome. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 14: 308-14. PMID 23286755 DOI: 10.3109/21678421.2012.751613  0.96
2013 Rivera I, Ajroud-Driss S, Casey P, Heller S, Allen J, Siddique T, Sufit R. Prevalence and characteristics of pain in early and late stages of ALS. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 14: 369-72. PMID 23286754 DOI: 10.3109/21678421.2012.751614  0.96
2013 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, et al. Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Neurobiology of Aging. 34: 357.e7-19. PMID 22959728 DOI: 10.1016/j.neurobiolaging.2012.07.017  0.96
2013 Siddique T, Deng HX, Ajroud-Driss S. Motor Neuron Disease Emery and Rimoin's Principles and Practice of Medical Genetics. 1-22. DOI: 10.1016/B978-0-12-383834-6.00141-5  0.96
2011 Siddique T, Ajroud-Driss S. Familial amyotrophic lateral sclerosis, a historical perspective. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology / Edited by the Gaetano Conte Academy For the Study of Striated Muscle Diseases. 30: 117-20. PMID 22106714  0.96
2011 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, et al. SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis. Archives of Neurology. 68: 1440-6. PMID 22084127 DOI: 10.1001/Archneurol.2011.250  0.96
2011 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. Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations. Archives of Neurology. 68: 1057-61. PMID 21825243 DOI: 10.1001/Archneurol.2011.178  0.96
2011 Ajroud-Driss S, Deng HX, Siddique T. Recent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2. Current Neurology and Neuroscience Reports. 11: 262-73. PMID 21327736 DOI: 10.1007/S11910-011-0185-Z  0.96
2010 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. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Annals of Neurology. 67: 739-48. PMID 20517935 DOI: 10.1002/Ana.22051  0.96
2009 Souayah N, Ajroud-Driss S, Sander HW, Brannagan TH, Hays AP, Chin RL. Small fiber neuropathy following vaccination for rabies, varicella or Lyme disease. Vaccine. 27: 7322-5. PMID 19808027 DOI: 10.1016/J.Vaccine.2009.09.077  0.96
2009 Ajroud-Driss S, Wolfe L, Sufit R. Amyotrophic lateral sclerosis and sarcoidosis. Muscle & Nerve. 40: 903. PMID 19697365 DOI: 10.1002/Mus.21421  0.96
2009 Ajroud-Driss S, Fecto F, Ajroud K, Yang Y, Donkervoort S, Siddique N, Siddique T. A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs. Neurogenetics. 10: 359-61. PMID 19350291 DOI: 10.1007/S10048-009-0188-Y  0.96
2008 Ajroud-Driss S, Sufit R, Siddique T, Hain TC. Oculomotor involvement in myotonic dystrophy type 2. Muscle & Nerve. 38: 1326-9. PMID 18785188 DOI: 10.1002/Mus.21113  0.96
2008 Frutiger K, Lukas TJ, Gorrie G, Ajroud-Driss S, Siddique T. Gender difference in levels of Cu/Zn superoxide dismutase (SOD1) in cerebrospinal fluid of patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 9: 184-7. PMID 18574763 DOI: 10.1080/17482960801984358  0.96
2007 Ajroud-Driss S, Saeed M, Khan H, Siddique N, Hung WY, Sufit R, Heller S, Armstrong J, Casey P, Siddique T, Lukas TJ. Riluzole metabolism and CYP1A1/2 polymorphisms in patients with ALS. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 8: 305-9. PMID 17852022 DOI: 10.1080/17482960701500650  0.96
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