Human C9ORF72 hexanucleotide expansion reproduces RNA foci and dipeptide repeat proteins but not neurodegeneration in BAC transgenic mice OM Peters, GT Cabrera, H Tran, TF Gendron, JE McKeon, J Metterville, ... Neuron 88 (5), 902-909, 2015 | 281 | 2015 |
Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis C Yang, H Wang, T Qiao, B Yang, L Aliaga, L Qiu, W Tan, J Salameh, ... Proceedings of the National Academy of Sciences 111 (12), E1121-E1129, 2014 | 206 | 2014 |
ALS‐linked protein disulfide isomerase variants cause motor dysfunction U Woehlbier, A Colombo, MJ Saaranen, V Pérez, J Ojeda, FJ Bustos, ... The EMBO journal 35 (8), 845-865, 2016 | 118 | 2016 |
Amyotrophic lateral sclerosis JS Salameh, RH Brown Jr, JD Berry Seminars in neurology 35 (04), 469-476, 2015 | 110 | 2015 |
Adeno‐associated virus–delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model L Stoica, SH Todeasa, GT Cabrera, JS Salameh, MK ElMallah, C Mueller, ... Annals of neurology 79 (4), 687-700, 2016 | 109 | 2016 |
Guillain–barre syndrome E Malek, J Salameh Seminars in neurology 39 (05), 589-595, 2019 | 104 | 2019 |
Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging F Tian, W Yang, DA Mordes, JY Wang, JS Salameh, J Mok, J Chew, ... Nature communications 7 (1), 13283, 2016 | 99 | 2016 |
A randomized trial of mexiletine in ALS: Safety and effects on muscle cramps and progression MD Weiss, EA Macklin, Z Simmons, AS Knox, DJ Greenblatt, N Atassi, ... Neurology 86 (16), 1474-1481, 2016 | 97 | 2016 |
Traumatic brain injury: oxidative stress and novel anti-oxidants such as mitoquinone and edaravone H Ismail, Z Shakkour, M Tabet, S Abdelhady, A Kobaisi, R Abedi, ... Antioxidants 9 (10), 943, 2020 | 94 | 2020 |
Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing TI Jones, C Yan, PC Sapp, D McKenna-Yasek, PB Kang, C Quinn, ... Clinical epigenetics 6, 1-16, 2014 | 83 | 2014 |
Medical research productivity in the Arab countries: 2007-2016 bibliometric analysis R El Rassi, LI Meho, A Nahlawi, JS Salameh, A Bazarbachi, EA Akl Journal of global health 8 (2), 2018 | 67 | 2018 |
Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosis OM Peters, EA Lewis, JM Osterloh, A Weiss, JS Salameh, J Metterville, ... Human Molecular Genetics 27 (21), 3761-3771, 2018 | 51 | 2018 |
An open label study of a novel immunosuppression intervention for the treatment of amyotrophic lateral sclerosis CN Fournier, D Schoenfeld, JD Berry, ME Cudkowicz, J Chan, C Quinn, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19 (3-4), 242-249, 2018 | 41 | 2018 |
Amyotrophic lateral sclerosis: analysis of ALS cases in a predominantly admixed population of Ecuador M Bucheli, A Andino, M Montalvo, J Cruz, N Atassi, J Berry, J Salameh Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15 (1-2), 106-113, 2014 | 38 | 2014 |
Necrotizing myopathies: an update C Quinn, JS Salameh, T Smith, N Souayah Journal of clinical neuromuscular disease 16 (3), 131-140, 2015 | 33 | 2015 |
Impaired neurodevelopment by the low complexity domain of CPEB4 reveals a convergent pathway with neurodegeneration J Shin, JS Salameh, JD Richter Scientific reports 6 (1), 29395, 2016 | 26 | 2016 |
A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1 YB Liu, A Tewari, J Salameh, E Arystarkhova, TG Hampton, A Brashear, ... Elife 4, e11102, 2015 | 25 | 2015 |
Phosphoglycerate mutase deficiency with tubular aggregates in a patient from Panama J Salameh, N Goyal, R Choudry, S Camelo‐Piragua, PST Chong Muscle & nerve 47 (1), 138-140, 2013 | 22 | 2013 |
Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice C Yang, T Qiao, J Yu, H Wang, Y Guo, J Salameh, J Metterville, S Parsi, ... PLoS One 17 (2), e0255710, 2022 | 17 | 2022 |
SOD1 (A4V)‐mediated ALS presenting with lower motor neuron facial diplegia and unilateral vocal cord paralysis JS Salameh, N Atassi, WS David Muscle & Nerve: Official Journal of the American Association of …, 2009 | 16 | 2009 |