| Year |
Citation |
Score |
| 2023 |
Berger A, Locatelli M, Arcila-Londono X, Hayat G, Olney N, Wymer J, Gwathmey K, Lunetta C, Heiman-Patterson T, Ajroud-Driss S, Macklin EA, Bind MA, Goslin K, Stuchiner T, Brown L, et al. The natural history of ALS: Baseline characteristics from a multicenter clinical cohort. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-9. PMID 37461167 DOI: 10.1080/21678421.2023.2232812 |
0.307 |
|
| 2019 |
Kacem I, Sghaier I, Bougatef S, Nasri A, Gargouri A, Ajroud-Driss S, Gouider R. Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-9. PMID 31858811 DOI: 10.1080/21678421.2019.1704012 |
0.352 |
|
| 2017 |
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, et al. Pyrimethamine Significantly Lowers CSF/SOD1 in ALS Patients With SOD1 Mutations. Annals of Neurology. PMID 28480639 DOI: 10.1002/Ana.24950 |
0.477 |
|
| 2017 |
Sufit RL, Ajroud-Driss S, Casey P, Kessler JA. Open label study to assess the safety of VM202 in subjects with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-10. PMID 28166654 DOI: 10.1080/21678421.2016.1259334 |
0.318 |
|
| 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 |
0.69 |
|
| 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 |
0.489 |
|
| 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 |
0.348 |
|
| 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 |
0.366 |
|
| 2012 |
Allen J, Hall M, Wallery S, Ajroud-Driss S, Armstrong J, McManus C, Cook T, Sufit R, Chrisman H, Wolfe L, Siddique T. Gastrostomy Tube Placement by Endoscopy Versus Radiologic Methods in Patients with ALS: A Retrospective Review of Complications and Outcome (P01.101) Neurology. 78: P01.101-P01.101. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P01.101 |
0.362 |
|
| 2012 |
Ajroud-Driss S, Fecto F, Ajroud K, Siddique T. Mutations in the Nuclear Encoded Novel Mitochondrial Protein CHCHD10 Cause an Autosomal Dominant Mitochondrial Myopathy (IN7-2.002) Neurology. 78: IN7-2.002-IN7-2.002. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In7-2.002 |
0.691 |
|
| 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 |
0.335 |
|
| 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 |
0.726 |
|
| 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 |
0.714 |
|
| 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 |
0.342 |
|
| 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 |
0.71 |
|
| 2009 |
Ajroud-Driss S, Wolfe L, Sufit R. Amyotrophic lateral sclerosis and sarcoidosis. Muscle & Nerve. 40: 903. PMID 19697365 DOI: 10.1002/Mus.21421 |
0.306 |
|
| 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 |
0.671 |
|
| 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 |
0.456 |
|
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